Compounds for using in imaging and particularly for the diagnosis of neurodegenerative diseases

Abstract

The invention relates to compounds of formula (II) for using in imaging and particularly for the diagnosis of neurodegenerative diseases.

Claims

1. Compound of formula II ##STR00414## X being selected from N or CR.sub.4 Y being selected from an alkene or an alkyne, an aryl or a heteroaryl, an alkane comprising from 1 to 7 carbon atoms, n being an integer equal to 0 or 1; R.sub.1 being selected from aryl or heteroaryl selected from phenyl, pyrimidine, pyridine, thiophene, furan, triazole, oxazole, (aza)indole, (aza)indoline, (aza)benzimidazole optionally substituted at one or more positions with a group selected from: Halogen, NO.sub.2, CN, dimethyltriazene, trimethylammonium, aryliodonium, NR.sup.aR.sup.b, SO.sub.2NR.sup.aR.sup.b, CONR.sup.aR.sup.b, NR.sup.cSO.sub.2NR.sup.aR.sup.b, NR.sup.cCONR.sup.aR.sup.b, NR.sup.aCOR.sup.b; R.sup.a, R.sup.b and R.sup.c are independently of each other H, (C.sub.1-C.sub.7) alkyl, aryl, heteroaryl, (C.sub.3-C.sub.7) carbocyclyl, (C.sub.1-C.sub.7) alkyl-aryl, (C.sub.1-C.sub.7) alkyl-heteroaryl, or R.sup.a and R.sup.b together form a (C.sub.3-C.sub.7) heterocyclyl; Sn (Alkyl).sub.3, Alkyl is selected from methyl or n-butyl; B(OH).sub.2, B(pinacol); R.sup.d, CH.sub.2R.sup.d; R.sup.d represents H, (C.sub.1-C.sub.7)alkyl, aryl, heteroaryl, (C.sub.3-C.sub.7) heterocyclyl, (C.sub.3-C.sub.7) carbocycIyIe, (C.sub.1-C.sub.7)alkyl-aryl, (C.sub.1-C.sub.7) alkyl-heteroaryl, (C.sub.1-C.sub.7) alkyl-(C.sub.3-C.sub.7) heterocyclyl, [(C.sub.1-C.sub.7) alkyl].sub.n-Z or a [(C.sub.1-C.sub.7) alkyl-Z].sub.n Z being a heteroatom selected from N, O or S, in particular selected from NR.sup.aR.sup.b or OR.sup.e, and n being an integer comprised from 1 to 7; OR.sup.e, OAc, OTs, OTf, SR.sup.e, SO.sub.2R.sup.e, COR.sup.e, NR.sup.eSO.sub.2R.sup.e, NHCOOR.sup.e; R.sup.e is H, (C.sub.1-C.sub.7)alkyl, aryl, heteroaryl, (C.sub.3-C.sub.7) heterocyclyl, (C.sub.3-C.sub.7) carbocyclyl, (C.sub.1-C.sub.7) alkyl-aryl, (C.sub.1-C.sub.7) alkyl-heteroaryl or (C.sub.1-C.sub.7) alkyl-(C.sub.3-C.sub.7) heterocyclyl; R.sub.2 being selected from: H, SO.sub.2Ph, COR.sup.e, NR.sup.cCONR.sup.aR.sup.b, COOR.sup.e, OH, R.sup.d; R.sub.3 being selected from: Halogen, NO.sub.2, CN, dimethyltriazene, trimethylammonium, aryliodonium, NR.sup.aR.sup.b, SO.sub.2NR.sup.aR.sup.b, CONR.sup.aR.sup.b, NR.sup.cSO.sub.2NR.sup.aR.sup.b, NR.sup.cCONR.sup.aR.sup.b, NR.sup.aCOR.sup.b; Sn(Alkyl).sub.3, Alkyl being selected from methyl or n-butyl; B(OH).sub.2, B (pinacol); R.sup.d, CH.sub.2R.sup.d; OR.sup.e, OAc, OTs, OTf, O(heteroaryl), especially O(HOBt), SR.sup.e, SO.sub.2R.sup.e, COR.sup.e, NR.sup.aSO.sub.2R.sup.e, NHCOOR.sup.e; R.sub.4 being selected from: Halogen, CH.sub.2NR.sup.aR.sup.b, R.sup.a, COOR.sup.e, CHO, CH.sub.2OR.sup.e; wherein at least one of the substituents R.sub.1, R.sub.2, R.sub.3 or R.sub.4 comprises a radioelement selected from .sup.18F, .sup.11C, .sup.123I and .sup.124I.

2. A compound according to claim 1 of the general formula II-1: ##STR00415## R.sub.1, R.sub.2, R.sub.3 and R.sub.4 being as previously defined in formula II; wherein at least one of the substituents R.sub.1, R.sub.2, R.sub.3 or R.sub.4 comprises a radioelement selected from .sup.18F, .sup.11C, .sup.123I and .sup.124I.

3. Compound according to claim 1, said compound being of general formula II-1: ##STR00416## R.sub.2, R.sub.3 and R.sub.4 being as previously defined in formula II; R.sub.1 being optionally labeled and selected from ##STR00417## n being in particular comprised from 0 to 6; ##STR00418## ##STR00419## ##STR00420## ##STR00421##

4. Compound according to claim 1, said compound being of general formula II-1: ##STR00422## R.sub.1, R.sub.3 and R.sub.4 being as previously defined in formula II; R.sub.2 being optionally labeled and selected from H; (CH.sub.2CH.sub.2O).sub.nCH.sub.2CH.sub.2F, n being an integer equal to 0, 1 or 2; SO.sub.2Ph; COO.sup.tBu; CH.sub.2OCH.sub.3; CH.sub.2O (CH.sub.2).sub.2OCH.sub.3; COCH.sub.3; ##STR00423##

5. Compound according to claim 1, said compound being of general formula II-1: ##STR00424## R.sub.1, R.sub.2 and R.sub.4 being as previously defined in formula II; R.sub.3 is optionally labeled and selected from 6-C1; 6-F; 5-F; 4-F; 6-(2-thienyl); 6-(3-thienyl); 6-(6-fluoro-3-pyridyl); 5-OMe; 6-morpholino; 5-morpholino; 6-Br; 4-Br; 4-Bpin; 5-Bpin.

6. Compound according to one of claim 1, said compound being of general formula II-1: ##STR00425## R.sub.1, R.sub.2 et R.sub.3 being as previously defined in formula II; R.sub.4 is selected from H; (CH.sub.2).sub.nN-alkyl, n being an integer equal to 0, 1 or 2.

7. Compound according to claim 1, said compound being of general formula II-1a: ##STR00426## R.sub.2, R.sub.3 and R.sub.4 being as previously defined in formula II; R.sub.1 being optionally labeled and is selected from ##STR00427## n being in particular from 0 to 6 ##STR00428## ##STR00429## ##STR00430## ##STR00431##

8. Compound according claim 1, said compound being of general formula II-2 ##STR00432## R.sub.1, R.sub.2 or R.sub.3 being as defined above in formula II; wherein at least one of the substituents R,, R.sub.2 or R.sub.3 comprises a radioelement selected from .sup.18F, .sup.11C, .sup.123I and .sup.124I.

9. Compound according to claim 1, said compound of formula II being chosen from compounds of the following formulas: ##STR00433## ##STR00434## ##STR00435## ##STR00436## ##STR00437## ##STR00438## ##STR00439## ##STR00440## ##STR00441## in a radio labelled state.

10. Method for diagnosing or in vivo imaging a subject having a neurodegenerative disease, comprising administering a compound of formula wherein at least one of the substituents R.sub.1, R.sub.2, R.sub.3 or R.sub.4 comprises a radioelement selected from .sup.18F, .sup.11C, .sup.123I and .sup.124I according to claim 1, to said subject.

11. Method for diagnosing or in vivo imaging a subject having a neurodegenerative disease, comprising administering a compound of formula II wherein at least one of the substituents R.sub.1, R.sub.2, R.sub.3 or R.sub.4 comprises a radioelement selected from .sup.18F, .sup.11C, .sup.123I and .sup.124I according to claim 1, to said subject, wherein the in vivo imaging method is positron emission tomography or single photon emission tomography.

12. Method for diagnosing or in vivo imaging a subject having a neurodegenerative disease, comprising administering a compound of formula II wherein at least one of the substituents R.sub.1, R.sub.2, R.sub.3 or R.sub.4 comprises a radioelement selected from .sup.18F, .sup.11C, .sup.123I and .sup.124I according to claim 1, to said subject, wherein said neurodegenerative disease is amyloidopathy, alpha-synucleinopathy or tauopathy.

Description

FIGURES

(1) FIG. 1a shows the preparation of synthons radiolabeled with carbon-11 1a) from carbon dioxide labeled with carbon-11 and 1b) from methane labeled with carbon-11.

(2) FIG. 2 shows the chemical functionalities radiolabeled with carbon-11 accessible via carbonylation reactions.

(3) FIG. 3 shows the quality control chromatograms of the compound [.sup.18F]28 with a double detection, A) radioactive signal) and B) ultraviolet at 360 nm.

(4) FIG. 4 shows the image obtained after the experiment described in Example 19.6 in PET/CT imaging, it is the cross section of the head of a rat after iv injection of the tracer and the sum of acquisitions between 50 and 180 min post-injection.

EXAMPLES

(5) General Procedures

Example 1 Procedure A (Protection of Azaindole with a Benzenesulfonyl Group)

Example 1.1

(6) A1: To a solution of NaH (2 eq.) in THF under argon and at 0 C. was added slowly a solution of azaindole (1 eq.) in THF (1 M). The mixture was stirred at room temperature for 30 min. After returning to 0 C., benzenesulfonyl chloride (1.2 eq.) was added dropwise. After stirring overnight at room temperature, the mixture was poured into a beaker with ice. After allowing to warm to room temperature, the phases were separated. The aqueous phase was extracted with ethyl acetate. The combined organic phases were washed with NaCl, dried over MgSO.sub.4 and concentrated under reduced pressure. The protected product was isolated either by filtration followed by washing the precipitate with diethyl ether or by flash column chromatography on silicagel.

Example 1.2

(7) A2: To a solution of azaindole (1 eq.) in 2-butanone (0.1 M) was added potassium carbonate (4 eq.) and benzenesulfonyl chloride (1.5 eq.). The mixture was stirred at 80 C. for 2 hours. The mixture was concentrated under reduced pressure and water and ethyl acetate were added. After phase separation, the aqueous phase was further extracted with ethyl acetate (3 times). The combined organic phases were washed with NaCl, dried over MgSO.sub.4 and concentrated under reduced pressure. The protected product was isolated either by filtration followed by washing the precipitate with diethyl ether or by flash column chromatography on silicagel.

Example 2. Procedure B (Lodation in C-2 Position of the Azaindole)

Example 2.1

(8) B1 (E. DESARBRE S. Coudret, C. Meheust, J Y Merour, Tetrahedron, 1997, 53 (10) 3637-3648; Joseph B., H. Da Costa J Y Merour, Ldonce S., Tetrahedron, 2000, 56, 3189-3196): Under argon atmosphere, to a solution of phenylsulfonylazaindole (1 eq) and TMEDA (1.05 eq) in THF (0.1 M), cooled to 25. C., was added dropwise a solution of LDA in THF (2M, 2 eq.). After 30 min, a solution of iodine (1M, 2 eq.) in THF was slowly added to the reaction medium via cannula. The reaction was followed by .sup.1H NMR and once the starting material was consumed, addition of water and extraction with ethyl acetate (3 times) were performed. The combined organic phase was dried over MgSO.sub.4 and concentrated under reduced pressure and purified by flash column chromatography on silicagel.

Example 2.2

(9) B2: Under argon atmosphere, to a solution phenylsulfonylazaindole (1 eq.) and TMEDA (1.1 eq) in THF (0.1M), cooled to 70 C., was added dropwise a solution of LDA (2M in THF, 1.7 eq.). After 30 min, a solution of iodine (2.2 eq.) in THF (1M) was slowly added to the reaction medium via cannula. The reaction was monitored by .sup.1H NMR After consumption of the starting material, water is added, and the aqueous phase was extracted with ethyl acetate (3 times). The combined organic phase was then dried over MgSO.sub.4, concentrated under reduced pressure and purified by flash column chromatography on silicagel.

Example 3: Procedure C (Sonogashira Coupling)

3.1 Example C

(10) The catalyst [Pd(PPh.sub.3).sub.4] (5 mol %) was added to a degassed solution of iodine azaindole derivative (1.0 eq.), alkyne (1.2 eq.) and CuI (10 mol %) in a mixture of Et.sub.3N/THF (1:1) at a concentration of 0.1 M. The mixture was heated at 50-60 C. for 4 h under argon atmosphere. After returning to room temperature, the mixture was poured into an aqueous solution of (10%) NH.sub.4Cl. After phase separation, the aqueous phase was further extracted with ethyl acetate (3 times 20 ml) and the combined organic phases were washed with NaCl, dried over MgSO.sub.4, filtered, concentrated under reduced pressure and purified by flash column chromatography on silicagel.

3.1 Example C2

(11) The catalyst [Pd(PPh.sub.3).sub.2Cl.sub.2] (5 mol %) was added to a degassed solution of iodine azaindole derivative (1.0 eq.), alkyne (1.2 eq.), CuI (10% mol) and Et.sub.3N (2.2 eq) in THF (C=0.1 M). The mixture was stirred at room temperature for 16 h under argon. The reaction mixture was concentrated under reduced pressure before being purified by flash column chromatography on silicagel.

Example 4. Procedure D (Desulfonylation of the Azaindole)

(12) (C. Chaulet, C. Cross, J. Basset, M.-D. Pujol, M.-C. Viaud-Massuard, Synlett. 2010, 10, 1481-1484)

(13) A dioxane solution containing the azaindole derivative (1 eq.) protected by a sulfonyl benzene group, was added sodium tert-butoxyde (1.5 eq.). The mixture was heated at 80 C. for 18 hours. The medium was concentrated under reduced pressure and the residue was dissolved in ethyl acetate and water. After decantation, the aqueous phase was extracted with ethyl acetate (3 times). The combined organic phases were dried over MgSO.sub.4 and concentrated under reduced pressure, prior to purifying the crude reaction product by flash column chromatography on silicagel.

Example 5. Procedure E (Protection of Azaindole with a Boc)

(14) A solution of azaindole (1 eq.), di-tert-butyl dicarbonate (1.5 eq.) and 4-DMAP (0.2 eq.) in THF (0.2 M) was stirred at room temperature overnight. The mixture was concentrated under reduced pressure and purified by flash column chromatography on silicagel.

Example 6. Procedure F (Deprotection of Boc)

(15) To a dichloromethane solution (0.05 M) containing the azaindolique product protected by the Boc group (1 eq.), cooled to 0 C. was added dropwise TFA (ratio TFA/dichloromethane=1/2), stirring at 0 C. was carried out with TLC monitoring. At the end of the reaction, the reaction mixture was neutralized with saturated aqueous NaHCO.sub.3. After decantation, the aqueous phase was extracted with dichloromethane (2 times). The combined organic phases were dried over MgSO.sub.4, concentrated under reduced pressure and purified by flash column chromatography on silicagel.

Example 7. Procedure G (Suzuki Couplings)

Example 7.1 G1

(16) A halogenated compound (1 eq.) was dissolved in dioxane under argon and the boronic acid (1.2 eq.), Cs.sub.2CO.sub.3 (1.2 eq.), as well as [Pd.sub.2(dba).sub.3] (5 mol-%) and ligand P(t-Bu).sub.3 (10 mol %) were added. The reaction mixture was stirred and irradiated under microwave conditions at 100 C. for 1 hour. After cooling, the mixture was concentrated under reduced pressure and the residue was purified by flash column chromatography.

Example 7.2 G2

(17) A halogenated compound (1 eq.) Was dissolved in a mixture DME/H.sub.2O (2/1) under argon, and the boronic acid (1.2 eq.), Na.sub.2CO.sub.3 (2 eq.) and [Pd(PPh.sub.3).sub.4] (5 mol %) were added. The reaction mixture was stirred and irradiated under microwave conditions at 120 C. for 30 min. After cooling, water was added, and the compound was extracted with dichloromethane (3 times). The organic phase was dried over MgSO.sub.4 and concentrated under reduced pressure before the residue was purified by flash column chromatography.

(18) Preparation of the Acetylenic Azaindole Derivatives

(19) General Scheme:

(20) ##STR00138##

Example 8. Synthesis of the Starting Azaindoles

(21) Among the various azaindoles, some were synthesized by preparation methods described in the literature. This is particularly the case of 4-azaindole (Ia), 6-azaindole (Ib), 6-chloro-7-azaindole (Ic) and 6-fluoro-7-azaindole (Id)

(22) TABLE-US-00001 TABLE 1 Starting Azaindoles embedded image 1a global yield 78% 0 1b global yield 50% 1c global yield 33% 1d global yield 5%

Example 8.1 Preparation of 4-azaindole

(23) 4-azaindole was prepared from 4-amino-2-bromopyridine in a two steps sequence:

(24) ##STR00143##

Preparation of 2-((trimethylsilyl ethynyl pyridin-3-amine 7

(25) Product 7 was obtained starting from 3-amino-2-bromopyridine 6 according to procedure C by stirring the mixture at 60 C. for 6 hours and was isolated with a yield of 80% by flash column chromatography (ethyl acetate/petroleum ether=5/95).

Preparation of 4-azaindole 1a

(26) Product 7 (1.96 g, 10.3 mtnol, 1 eq.) was subjected to a cyclization reaction in the presence of a 1M THF solution potassium-tert-butoxide (10.3 ml, 10.3 mmol, 1 eq.) in CH.sub.3CN (15 ml) at room temperature for 2 hours. The mixture was then diluted with ethyl acetate and hydrolyzed with water. After decantation, the organic phase was washed with saturated aqueous NaCl solution, dried over MgSO.sub.4 and concentrated under reduced pressure. 4-azaindole was isolated by flash column chromatography on silicagel (ethyl acetate/petroleum ether=1/1) with a yield of 97%.

Example 8.2 Preparation of 6-azaindole 1b

(27) 6-azaindole was prepared from 3-amino-4-methylpyridine by a 3-step sequence described by Hands (D. Hands, B. Bishop, M. Cameron, J S Edwards, I F Cottrell, S H B Wright, Synthesis, 1996, 7, 877-882)

(28) ##STR00144##

Preparation of tert-butyl (4-methylpyridin-3-yl) carbamate 9

(29) To a solution of 3-amino-4-methylpyridine (2 g, 18.5 mmol, 1 eq.) in THF (35 ml) under argon at 0 C., was slowly added a 1M solution of NaHMDS/THF (40.7 ml, 40.7 mmol, 2.2 eq.). Boc.sub.2O (4.8 g, 22.2 mmol, 1.2 eq.) Was added and the ice bath was removed. The mixture was stirred 1 h30 at room temperature, the solvent was evaporated, and the residue was taken up in dichloromethane and washed with an aqueous HCl solution (50 ml), followed by a saturated NaCl solution. The organic phase was dried over MgSO.sub.4 and concentrated under reduced pressure, prior to isolation of 9 (2.4 g) after flash column chromatography on silicagel (ethyl acetate/petroleum ether=30/70) with a 62% yield.

tert-butyl Preparation of 2-hydroxy-2,3-dihydro-1H-pyrrolo[2,3-c]pyridine-1-carboxylate 10

(30) To a solution of tert-butyl(4-methylpyridin-3-yl) carbamate 9 (2.4 g, 11.5 mmol, 1 eq.) in THF (100 ml), cooled to 70 C., was added dropwise a solution 2.2 M nBuLi/hexanes (1 1.5 ml, 25.4 mmol, 2.2 eq.). After addition, the temperature was allowed to rise to 30 C. and maintained at that temperature with stirring for 2 h30. Then, DMF (1.34 ml, 17.3 mmol, 1.5 eq.) was added and the mixture was allowed to return to room temperature. After stirring for 3 hours at room temperature, water (100 ml) was added and the product was extracted with ethyl acetate (100 ml). The combined organic phases were washed with saturated NaCl solution, dried over MgSO.sub.4 and concentrated under reduced pressure before being purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=1/1) affording the desired product 10 in 99% yield (2.68 g).

Preparation of 6-azaindole 1b

(31) To a solution of t tert-butyl 2-hydroxy-2,3-dihydro-pyrrolo[2,3-c]pyridine-1-carboxylate 10 (2.68 g, 1 1.3 mmol, 1 eq.) in THF (45 ml) was added a 4N HCl solution in dioxane (15.6 ml, 62.4 mmol, 5.5 eq.). The mixture was stirred at 50 C. for 4 h30. The reaction mixture was neutralized with 5M aqueous NaOH solution (15.8 ml, 79.4 mmol, 7 eq.) and the aqueous phase was extracted with ethyl acetate (3 times). The combined organic phases were dried over MgSO.sub.4, concentrated under reduced pressure and purified by flash column chromatography on silicagel (solvent used: ethyl acetate) to give the desired product Ib in a yield of 81% (1.09 g).

Example 8.3 Preparation of 6-chloro-7-azaindole

(32) The 6-chloro-7-azaindole was prepared by a 3-step sequence described by Minakata (S. Minakata, M. omatsu, Y. Ohshiro, Synthesis, 1992, 7, 661-663):

(33) ##STR00145##

Preparation of N-Oxide 11

(34) To a solution of 7-azaindole (2 g, 16.9 mmol, 1 eq.) in ethyl acetate (60 ml) at 0 C., mCPBA (6.3 g, 25.6 mmol, 1.5 eq.) was added. The medium was stirred at room temperature for 2 hours. The reaction mixture was then put in an ice bath and the formed precipitate was isolated by filtration and washed with diethyl ether. Then, water was added to the tan solid and the medium was basified to pH=9 with a saturated solution of K.sub.2CO.sub.3. The mixture was placed in the refrigerator and filtered cold the next day. The filtrate was concentrated and cooled to repeat the operation to give after assembling the different batches, a white solid with a yield of 63% (1.43 g).

Preparation of ethyl 6-chloro-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 12

(35) To a solution of 11 (3.05 g, 22.7 mmol, 1 eq.) and HMDS (3.67 g, 22.7 mmol, 1 eq.) in THF was added dropwise methyl chloroformate (5.42 ml, 56.8 mmol, 2.5 eq.). The medium was stirred for 1 hour at room temperature and concentrated under reduced pressure. The residue obtained was dissolved in ethyl acetate, the organic phase is washed with a saturated solution of NaHCO.sub.3, dried over MgSO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography on gel silica (ethyl acetate/petroleum ether=1/1) to give the desired product 12 with a 99% yield (2.68 g).

Preparation of 6-chloro-7-azaindole

(36) To a solution of 12 (0.302 g, 1.4 mmol, 1 eq.) in MeOH (25 ml) was added a 1N solution of NaOH (1 1 ml). The mixture was stirred at room temperature for 6 hours, neutralized with a saturated solution of NaHCO.sub.3 and concentrated under reduced pressure. The precipitate was washed with water, filtered and dried under reduced pressure to give with 92% yield (0.2 g).

Example 8.4 Preparation of 6-fluoro-7-azaindole Id

(37) 6-fluoro-7-azaindole Id was prepared by a 5-step method from 2-amino-6-fluoropyridine (A. Stoit, H. K. A. C. Coolen, M. A. W. Van Der Neut, C. G. Kruse, Preparation of azaindoles with a combination of partial nicotinic acetylcholine receptor agonism and dopamine reuptake inhibitory activity PCT Int. Appl. 2008, WO 2008003736 A1 Jan. 10, 2008)

(38) ##STR00146##

Preparation of ethyl (6-fluoropyridin-2-yl) carbamate 13

(39) To a solution containing 2-amino-6-fluoropyridine (5 g, 44.6 mmol, 1 eq.) in CH.sub.3CN (110 ml) were added K.sub.2CO.sub.4 (18.5 g, 133.8 mmol, 3 eq.) and ethyl chloroformate (4.3 ml, 44.6 mmol, 1 eq.). The mixture was stirred at 40 C. for 4 days. Then, an additional portion of ethyl chloroformate (4.3 ml, 44.6 mmol, 1 eq.) was added and the mixture was stirred at 40 C. for 2 days. After returning to room temperature, ethyl acetate was added and the organic phase was washed with a saturated solution of NaHCO.sub.3, dried over MgSO.sub.4, filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90) to afford the desired product 13 in a yield of 68% (5.62 g). .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.83 (dd, J=8.0 Hz, J=2.0 Hz, 1H), 7.77 (m, 1H), 7.45 (bs, 1H), 6.59 (m, 1H), 4.25 (q, J=8.0 Hz, 2H), 1.32 (t, J=8.0 Hz, 3H).

Preparation of ethyl (6-fluoro-3-iodopyridin-2-yl) carbamate 14

(40) To a solution of 13 (5.6 g, 30.4 mmol, 1 eq.) in THF (80 ml), TMEDA (11.3 ml, 76.0 mmol, 2.5 eq.) was added and the mixture was cooled to 78 C. under argon. Then, a solution of n-BuLi (1.6 M in THF, 50 ml, 79.1 mmol, 2.6 eq.) was slowly added and the mixture was stirred at 78 C. for 2 hours. A solution of iodine (18 g, 70.9 mmol, 2.3 eq.) in THF (20 ml) was added via cannula. After stirring for stirring at 78 C., a saturated aqueous solution of Na.sub.2S.sub.20.sub.3 was added. After returning to room temperature, ethyl acetate was added and the separated organic phase was washed with a saturated aqueous solution of NaHCO.sub.3, dried over MgSO.sub.4 and concentrated under reduced pressure before the residue was purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90) to provide the desired product 14 with a 64% yield (6.03 g). .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.07 (t, J=8.0 Hz, 1H), 7.19 (bs, 1H), 6.49 (dd, J=8.0 Hz, J=3.0 Hz, 1H), 4.29 (q, J=8.0 Hz, 2H), 1.35 (t, J=8 Hz, 3H).

Preparation of ethyl (6-fluoro-3-((trimethylsilyl)ethynyl)pyridin-2-yl)carbamate 15

(41) [Pd(PPh.sub.3).sub.2]Cl.sub.2 (0.68 g, 0.97 mmol, 0.05 eq.) was added to a degassed solution containing derivative 14 (6.03 g, 19.5 mmol, 1 eq.), allyltrimethylsilane (4.9 ml, 35.0 mmol, 1.2 eq) and CuI (0.37 g, 1.95 mmol, 0.1 eq) in a mixture of 20 ml of Et.sub.3N/DMF (1/1). The mixture was heated at 100 C. for 30 hours under argon. After returning to room temperature, the mixture was poured into an ethyl acetate solution and H.sub.2O. After decantation, the organic was washed with H.sub.2O, dried over MgSO.sub.4 and concentrated under reduced pressure before being purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=5/95) and providing compound 15 in a yield of 15 43% (2.32 g). .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.76 (t, J=8.0 Hz, 1H), 7.64 (is, 1H), 6.56 (dd, J=8.0 Hz, J=3.0 Hz, 1H), 4.29 (q, J=8.0 Hz, 2H), 1.34 (t, J=8.0 Hz, 3H), 0.3 (s, 9H).

Preparation of ethyl 6-fluoro-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 16

(42) A mixture of derivative 15 (2.32 g, 8.3 mmol, 1 eq.) and CuI (3.15 g, 16.5 mmol, 2 eq.) in DMF (40 ml) was degassed under argon for 30 minutes. Then, the reaction mixture was heated at 150 C. for 30 minutes. After cooling, the mixture was diluted with ethyl acetate and filtered. The residue is washed with H.sub.2O, dried over MgSO.sub.4, filtered and concentrated under reduced pressure before being purified by flash column chromatography on silicagel (ethyl acetate/diethyl ether=1/1) to provide 16 with a 30% yield (0.52 g). .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.95 (t, J=8.0 Hz, 1H), 7.69 (d, J=4.0 Hz, 1H), 6.87 (dd, J=8.0 Hz, J=2.0 Hz, 1H), 6.57 (d, J=4.0 Hz, 1H), 4.55 (q, J=8.0 Hz, 2H), 1.49 (t, J=8.0 Hz, 3H).

Preparation of 6-fluoro-7-azaindole Id

(43) To a solution of 16 (1.3 g, 6.2 mmol, 1 eq.) in MeOH (25 ml) was added a 2N aqueous solution of NaOH (10 ml). The mixture was stirred for 30 minutes at room temperature and ethyl acetate was added. After decantation, the organic phase was washed with a 5% solution of NaHCO.sub.3, dried over MgSO.sub.4), filtered and concentrated under reduced pressure to provide Id with a 99% yield (0.84 g). .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 9.6 (bs, 1H), 7.95 (t, J=8.0 Hz, 1H), 7.29 (m, 1H), 6.75 (dd, J=8.0 Hz, J=2.0 Hz, 1H), 6.53 (m, 1H).

Example 9. Synthesis of N-Benzenesulfonyl Azaindole

Example 9.1 Synthesis of Derivatives of N-Benzenesulfonyl Azaindol Described in the Literature

(44) Commercial azaindoles and those prepared above were protected by the benzenesulfonyl group as described in one of two alternative general methods (A1 and A2). Table 2 below includes the compounds 1-(phenylsulfonyl)-1H-pyrrolo[2,3-b] pyridine 2a (S.-F. Liu, Q. Wu, H. L. Schmider H. Aziz, N.-X. Hu, Z. Popovic, S. Wang, J Am. Chem. Soc. 2000, 122, 3671-3678), 1-(phenylsulfonyl)-1H-pyrrolo[3,2-c] pyridine 2b (Mr. Lefoix, J.-P. Daillant S. Road, J Y Merour I. Gillaizeau G. Coudert, Synthesis, 2005, 20, 3581-3588), 1-(phenylsulfonyl)-1H-pyrrolo[3,2-b] pyridine 2c (D. C. Brookings, R. J. Cubbon, J. M. Davis, B. J. Langham. Preparation of pyrrolo[3,2-b]pyridines as p38 kinase inhibitors. PCT Int. Appl., 2004031188, 15 Apr. 2004), 1-(phenylsulfonyl)-1H-pyrrolo[2,3-c]pyridine 2d (Y. Horiguchi, H. Imoto, M. A. Wolf. Preparation of 6-azaindoles as IB kinase inhibitors for treating diabetes and inflammatory diseases. PCT Int. Appl., 2005097129, 20 Oct. 2005), 6-chloro-1-(phenylsulfonyl)-1H-[2,3-b]pyridine 2e (Y.-S. Tung, M. S. Coumar, Y.-S. Wu, H.-Y. Shiao, J.-Y. Chang, J.-P. Liou, P. Shukla, C.-W. Chang, C.-Y. Chang, C.-C. Kuo, T.-K. Yeh, C.-Y. Lin, J.-S. Wu, S.-Y. Wu, C.-C. Liao, H.-P. Hsieh, J. Med. Chem. 2011, 54, 3076-3080), 6-fluoro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 2f (A. R. Stoit, A. P. den Hartog, H. Mons, S. van Schaik, N. Barkhuijsen, C. Stroomer, H. K. A. C. Coolen, J. H. Reinders, T. J. P. Adolfs, M. van der Neut, H. Keizer, C. G. Kruse, Bioorg. Med. Chem. Lett. 2008, 18, 188-193), 5-fluorouracil-1-(phenylsulfonyl)-1H-pyrrolo[2,3-i] pyridin 2 g (S. J. Berthel, L. Chen, W. L. Corbett, L. C. Feng, N.-E. Haynes, R. F. Kester, S. S. So, J. Wright Tilley. Azaindole derivatives as glucokinase activators and their preparation and use in the treatment of metabolic disorders. U.S. Pat. Appl. Publ., 20110144105, 16 Jun. 2011), 6-bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 2i (A. Stoit, H. K. A. C. Coolen, M. A. W. Van Der Neut, C. G. Kruse, Azaindole derivatives with a combination of partial nicotinic acetylcholine receptor agonism and dopamine reuptake inhibition, US 2008/0009514 A1 Jan. 10, 2008), 5-bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b] pyridine 2j (N. Liu, Y Wang, G. Huang, C. Ji. W. Fan, H. Li, Y. Cheng, H. Tian, Bioorg. Chem. 2016, 65, 146-158) and 4-chloro-1-(phenylsulfonyl)-IH-pyrrolo[2,3-b]pyridine 2k (H.-Q. Dong, K. Foreman, A.-H. Li, M. J. Mulvihill, B. Panicker, A. G. Steinig, K. M. Stolz, Q. Weng, M. Jin, B. Volk, J. Wang, T. Wang, J. D. Beard, Pyrrolopyridine kinase inhibiting compounds, US 2007/0129364 A1 Jun. 7, 2007)

(45) TABLE-US-00002 TABLE 2 N-benzenesulfonyl azaindoles embedded image 2a, 90% Procedure A1 2b, 92% Procedure A2 2c, 79% Procedure A2 0 2d, 85% Procedure A2 2e, 96% Procedure A2 2f, 89% Procedure A1 2g, 80% Procedure A1 2h, 98% Procedure A1 2i, 97% Procedure A1 2j, 91% Procedure A1 2k, 96% Procedure A1

Example 10. Synthesis Iodated Azaindole Derivatives

(46) The different iodated derivatives were prepared by appropriate general procedures. The compounds 2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b] pyridine 3a, 2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridine 3b, were obtained good yields of 83 and 60% respectively

(47) TABLE-US-00003 embedded image 3a, 83% Procedure B1 3b, 60% Procedure B1 0 3c, 70% Procedure B1 3d, 67% Procedure A2 3e, 65% Procedure B2 18f 56% 2 steps Procedures B2/D 18g 48% 2 steps Procedures B2/D 18h 73% 2 steps Procedure B2/D 18i, 90% 3j, 93% Procedure B2 18k 3% 2 steps Procedures B1/D 18l 58% 2 steps Procedure B1/D

(48) 2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[3,2-b]pyridine 3c was prepared following procedure B1, however, under the same conditions its isomer 2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-c] pyridine 3d led to the formation of a non-separable mixture of the desired product 3d and di-iodated product 17d. the mixture was isolated by extraction and engaged in a desulfonylation reaction according to procedure D to afford the product 18d with a 47% yield over 2 steps. The latter was protected according to procedure A2 to obtain the desired product 3d

(49) ##STR00170##

(50) The iodated derivative of 6-chloro-7-azaindole 3 was prepared according to procedure B1 with a moderate yield of 46%, which was improved to 65% using procedure B2. But its brominated 3d was obtained with an excellent yield of 93% according to procedure B2.

(51) Procedure B2 starting from compounds 2f-h provided fluorinated derivatives of 7-azaindole 3f-h in a mixture with with di-iodated products 17f and 19f-h. After application of desulfonylation procedure D, derivatives 18f-h were isolated alone and used directly in Sonogashira coupling reactions.

(52) ##STR00171##

(53) The desulfonylation of type 3 azaindoles has been completed according to procedure D, the type 18 products have then undergone a protection step by a protective group Boc generating 20 (E procedure)

(54) ##STR00172##

(55) TABLE-US-00004 TABLE 4 Iiodated derivatives of azaindoles obtained according to procedures D or E. embedded image 18a, 85% Procedure D 18b, 65% Procedure D 18e, 61% Procedure D 18j, 87% Procedure D 20a, 94% Procedure E 20b, 88% Procedure E 20e, 99% Procedure E 0 20j, 99% Procedure E

Example 10.1 2-Iodo-1-(phenylsulfonyl)-LH-pyrrolo[3,2-d] pyridine 3c

(56) ##STR00181##

(57) The compound was prepared according to procedure B1 and purified by flash chromatography column on silicagel (ethyl acetate/petroleum ether=25/75). Yellow solid (70%), mp 138-140 C., R.sub.s=0.27 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3704, 3061, 2360, 1566, 1502, 1479, 1450, 1405, 1375, 1268, 1213, 1191, 1166, 1125, 1090, 998, 802, 781, 756, 724, 682, 668, 584, 558, 524, 509. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.59-8.45 (m, 2H), 7.95-7.83 (m, 2H), 7.61 (m, 1H), 7.52-7.40 (m, 2H), 7.21 (m, 2H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 149.1 (Cq), 146.6 (CH), 137.9 (Cq), 134.5 (CH), 132.3 (Cq), 129.4 (2CH), 127.3 (2CH), 124.8 (CH), 122.5 (CH), 119.3 (CH), 81.0 (Cq). HRMS (+ESI) calculated for C.sub.13H.sub.10IN.sub.2O.sub.2S (M+H+): 384.9502, found: 384.9503.

Example 10.2 2-Iodo-1-(phenylsulfonyl)-LH-pyrrolo[2,3-c] pyridine 3d

(58) ##STR00182##

(59) The compound was prepared according to procedure A2 and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=30/70). Yellow solid (67%), mp 149 151 C., Rf=0.34 (ethyl acetate/petroleum ether=1/1). IR (v, cm.sup.1, neat) 3091, 2919, 2842, 2735, 1639, 1612, 1592, 1540, 1480, 1450, 1416, 1379, 1319, 1272, 1205, 1170, 1124, 1109, 1091, 1049, 1031, 1014, 996, 899, 834, 819, 755, 725, 684, 668, 607, 559, 514. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 9.53 (t, J=0.9 Hz, 1H), 8.39 (d, J=5.3 Hz, 1H), 8.03-7.86 (m, 2H), 7.61 (m, 1H), 7.55-7.41 (m, 2H), 7.35 (dd, J=5.3 Hz, J=1.1 Hz, 1H), 7.00 (d, J=0.8 Hz, 1H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 142.8 (CH), 137.7 (Cq), 137.2 (CH), 136.7 (Cq), 135.6 (Cq), 134.5 (CH), 129.4 (2CH), 127.4 (2CH), 122.4 (CH), 113.7 (CH), 81.9 (Cq). HRMS (+ESI) calculated for C.sub.13H.sub.10IN.sub.2O.sub.2S (M+H+): 384.9502, found: 384.9507.

Example 10.3 3 6-Chloro-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 3e

(60) ##STR00183##

(61) The compound was prepared according to procedure B2 and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). White solid (46%), mp 176-178 C., Rf=0.39 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3115, 2954, 1907, 1570, 1486, 1435, 1374, 1336, 1277, 1240, 1207, 1177, 1126, 1089, 1012, 928, 825, 756, 724, 684, 631, 588, 558, 545, 521. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.32-8.19 (m, 2H), 7.70-7.41 (m, 4H), 7.14 (d, J=8.2 Hz, 1H), 6.95 (s, 1H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 147.7 (Cq), 146.1 (Cq), 138.1 (Cq), 134.4 (CH), 129.6 (CH), 129.0 (2CH), 128.5 (2CH), 122.2 (Cq), 119.7 (CH), 119.4 (CH), 75.9 (Cq). HRMS (+ESI) calculated for C.sub.13H.sub.9C.sub.1N.sub.2O.sub.2S (M+H+): 418.9113, found: 418.9111.

Example 10.4 10.4 6-Bromo-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 3j

(62) ##STR00184##

(63) The compound was prepared according to procedure B2 and purified by chromatography column on silicagel under pressure (the ratio of solvents used: ethyl acetate/petroleum ether=10/90). White solid (93%), mp 205-207 C., Rf=0.43 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3383, 2359, 1635, 1588, 1567, 1485, 1449, 1430, 1370, 1333, 1275, 1235, 1207, 1175, 1129, 1114, 1087, 1011, 918, 826, 755, 723, 697, 684, 623, 585, 557, 537, 502. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.35-8.01 (m, 2H), 7.69-7.37 (m, 4H), 7.25 (m, IH), 6.91 (s, IH). 13C NMR (63 MHz, CDCl.sub.3, 20 C.) 148.0 (Cq), 138.1 (Cq), 136.1 (Cq), 134.4 (CH), 129.4 (CH), 129.0 (2*CH), 128.7 (2CH), 123.3 (CH), 122.4 (Cq), 119.5 (CH), 76.0 (Cq). HRMS (+ESI) calculated for C.sub.3H.sub.9 strand.sub.2 0.sub.2 S (M H+): 464.8587, found: 464.8581.

Example 10.5 2-Iodo-1H-pyrrolo[2,3-b]pyridine 18a

(64) ##STR00185##

(65) The compound was prepared according to procedure D and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). White solid (85%), mp 189-191 C., Rf=0.43 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 2790, 1580, 1481, 1431, 1403, 1336, 1308, 1275, 911, 812, 762, 622, 510. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.20 (s, 1H), 8.13 (dd, J=4.7 Hz, J=1.6 Hz, 1H), 7.86 (dd, J=7.8 Hz, J=1.6 Hz, 1H), 7.02 (dd, J=7.8 Hz, J=4.7 Hz, 1H), 6.70 (s, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 151.0 (Cq), 142.9 (CH), 126.9 (CH), 122.1 (Cq), 116.3 (CH), 110.0 (CH), 81.1 (Cq). HRMS (+ESI) calculated for C.sub.7H61N.sub.2 (M+H+): 244.9570, found: 244.9570.

Example 10.6 2-Iodo-1H-pyrrolo[3,2-c] pyridine 18b

(66) ##STR00186##

(67) The compound was prepared according to procedure D and isolated by precipitation in Et.sub.2 0 with a filtration. White solid (65%), mp 247-249 C., Rf=0.19 (ethyl acetate/petroleum ether=30/70) IR (v, cm.sup.1, neat) 3349, 3120, 3080, 3044, 2930, 2770, 2733, 2690, 2644, 1668, 1606, 1574, 1504, 1447, 1423, 1324, 1292, 1248, 1201, 1182, 1168, 1101, 1028, 948, 908, 838, 808, 796, 753, 629, 604, 537, 522, 518, 514, 511. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.08 (s, 1H), 8.73 (s, 1H), 8.09 (d, J=5.6 Hz, 1H), 7.29 (d, J=5.6 Hz, 1H), 6.81 (s, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) .sup.13C NMR (101 MHz, DMSO) 142.3 (Cq), 141.6 (CH), 140.6 (CH), 127.0 (Cq), 110.3 (CH), 106.3 (CH), 81.5 (Cq). HRMS (+ESI) calculated for C.sub.7H61N.sub.2 (M+H+): 244.9570, found: 244.9568.

Example 10.7 2Iodo1H-pyrrolo[3,2-b] pyridine 18c

(68) ##STR00187##

(69) The compound was prepared according to procedure D and purified by flash column chromatography on silicagel (acetone/dichloromethane=3/97). White solid (73%), mp 192-1 C. 4, Rf=0.31 (acetone/dichloromethane=2/98). IR (v, cm.sup.1, neat) 3052, 2950, 2871, 2644, 1613, 1563, 1504, 1481, 1432, 1393, 1352, 1309, 1282, 1195, 1118, 908, 769, 622, 578, 512, 502. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 11.91 (s, 1H), 8.26 (dd, J=4.6 Hz, J=1.4 Hz, 1H), 7.68 (dd, J=8.3 Hz, J=1.4 Hz, 1H), 7.03 (dd, J=8.3 Hz, J=4.6 Hz, 1H), 6.80 (s, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 147.7 (Cq), 143.2 (CH), 132.0 (Cq), 117.8 (CH), 116.8 (CH), 111.6 (CH), 84.6 (Cq). HRMS (+ESI) calculated for C.sub.7H.sub.6IN.sub.2 (M+H+): 244.9570, found: 244.9573.

Example 10.8 2-Iodo-1H-pyrrolo[2,3-c] pyridine 18d

(70) ##STR00188##

(71) The compound was prepared according to procedure B1 and procedure I and purified by flash column chromatography on silicagel (ethyl acetate). yellow solid (47% over 2 steps), mp 210-212 C., Rf=0.26 (ethyl acetate/petroleum ether=1/1). IR (v, cm.sup.1, neat) 2583, 1611, 1516, 1433, 1400, 1297, 1218, 1155, 1031, 910, 817, 630, 598, 512. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.21 (large s, 1H), 8.64 (s, 1H), 8.04 (m, 1H), 7.45 (d, J=5.3 Hz, 1H), 6.73 (s, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 138.5 (Cq), 136.7 (Cq), 134.0 (Cq), 133.4 (CH), 113.5 (CH), 110.5 (2CH).

(72) HRMS (+ESI) calcule pour C.sub.7H.sub.6IN.sub.2 (M+H+): 244.9570, trouve: 244.9573

Example 10.9 6-Chloro-2-iodo-1H-pyrrolo[2,3-b]pyridine 18e

(73) ##STR00189##

(74) The compound was prepared according to procedure D and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=3/97). White solid (61%), mp 208-210 C., Rf=0.40 (ethyl acetate/petroleum ether=3/97). IR (v, cm.sup.1, neat) 3103, 3024, 2938, 2852, 2806, 1596, 1575, 1474, 1409, 1387, 1332, 1285, 1265, 1124, 1111, 1092, 965, 933, 812, 752, 690, 630, 607, 517, 506. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.44 (s, 1H), 7.92 (d, J=8.2 Hz, 1H), 7.09 (d, J=8.2 Hz, 1H), 6.76 (s, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 149.6 (Cq), 143.5 (Cq), 130.1 (CH), 121.0 (Cq), 116.2 (CH), 110.4 (CH), 81.8 (Cq). HRMS (+ESI) calculated for C.sub.7H.sub.5ClIN.sub.2 (M+H+): 278.9181, found 278.9177.

Example 10.10 6-Fluoro-2-iodo-1H-pyrrolo[2,3-b]pyridine 18f

(75) ##STR00190##

(76) The compound was prepared according to procedure B2 and procedure D and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=3/97). White solid (56% over 2 steps), mp 172-174 C., Rf=0.34 (ethyl acetate/petroleum ether=5/95). IR (v, cm.sup.1, neat) 3134, 1589, 1424, 1343, 1272, 1199, 1105, 995, 811, 757, 614. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.34 (s, 1H), 8.02 (t, J=8.3 Hz, 1H), 6.79 (d, J=8.3 Hz, 1H), 6.76 (s, 1H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 161.3 (Cq), 147.0 (d, J=18.8 Hz, Cq), 132.2 (d, J=9.4 Hz, CH), 120.2 (Cq), 110.5 (CH), 101.6 (d, J=38.9 Hz, CH), 79.4 (Cq). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 76.0.

(77) HRMS (+ESI) calculated for C.sub.7H.sub.5FIN.sub.2 (M+H+): 262.9476, found: 262.9475.

Example 10.11 5-Fluoro-2-iodo-1H-pyrrolo[2,3-b]pyridine 18 g

(78) ##STR00191##

(79) The compound was prepared according to procedure B2 and procedure D and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=5/95). White solid (48% over 2 steps), mp 199-201 C., Rf=0.32 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3105, 3038, 2952, 2911, 2863, 2786, 2738, 2709, 2361, 1759, 1609, 1586, 1565, 1500, 1425, 1387, 1321, 1290, 1237, 1194, 1093, 1009, 978, 897, 877, 802, 760, 630, 590, 541, 505. RMN .sup.1H (250 MHz, DMSO-d.sub.6, 20 C.) 12.38 (s, 1H), 8.13 (m, 1H), 7.77 (dd, J=9.3 Hz, J=2.4 Hz, 1H), 6.71 (m, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 155.3 (d, J=239.7 Hz, Cq), 147.9 (Cq), 131.0 (d, J=29.0 Hz, CH), 122.0 (d, J=7.3 Hz, Cq), 112.5 (d, J=20.9 Hz, CH), 110.0 (d, J=4.0 Hz, CH), 83.9 (Cq). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 139.0. HRMS (+ESI) calculated for C.sub.7H.sub.5FIN.sub.2 (M+H+): 262.9476, found: 262.9473.

Example 10.12 4-fluoro-2-iodo-1H-pyrrolo[2,3-b]pyridine 18 h

(80) ##STR00192##

(81) The compound was prepared according to the sequence of procedures B2 and D and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20:80) Solid. white (73% over 2 steps), mp 218-220 C., Rf 0.26 (ethyl acetate/petroleum ether=20:80). IR (v, cm.sup.1, neat) 2724, 1628, 1570, 1511, 1479, 1432, 1395, 1336, 1311, 1273, 1253, 1113, 1049, 874, 806, 746, 616, 511. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.57 (s, 1H), 8.14 (s, 1H), 6.92 (d, J=4.0 Hz, 1H), 6.78 (s, 1H). RMN .sup.13C (101 MHz, DMSO-d.sub.6, 20 C.) 159.67 (d, J=260.5 Hz, Cq), 154.4 (d, J=11.4 Hz, Cq), 145.0 (d, J=6.1 Hz, CH), 110.9 (d, J=18.0 Hz, Cq), 105.6 (CH), 102.8 (d, J=14.8 Hz, CH), 81.6 (Cq). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 112.3. HRMS (+ESI) calculated for C.sub.7H.sub.5FIN.sub.2 (M+H+): 262.9476, found: 262.9475.

Example 10.13 6-Fluoro-2-iodo-1-methyl-1H-pyrrolo[2,3-b]pyridine 18i

(82) ##STR00193##

(83) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=1/99). White solid (90%), mp 94-96 C., Rf=0.27 (ethyl acetate/petroleum ether=5/95). IR (v, cm.sup.1, neat) 3111, 1602, 1574, 1472, 1441, 1404, 1333, 1301, 1265, 1230, 1125, 1091, 1041, 973, 820, 777, 748, 690, 580, 564, 516, 506, 503. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.84 (m, 1H), 6.79 (s, 1H), 6.66 (dd, J=8.4 Hz, J=1.1 Hz, 1H), 3.78 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 159.9 (d, J=237.5 Hz, Cq), 145.1 (d, J=17.5 Hz, Cq), 131.7 (d, J=9.4 Hz, CH), 119.5 (d, J=2.9 Hz, Cq), 110.3 (CH), 101.6 (d, J=38.8 Hz, CH), 83.4 (d, J=4.1 Hz, Cq), 32.6 (CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) 75.0. HRMS (+ESI) calculated for C.sub.5H.sub.7FIN.sub.2 (M+H+): 276.9633, found: 276.9633.

Example 10.14 6-Bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine 18j

(84) ##STR00194##

(85) The compound was prepared according to procedure D and purified by pressurized silicagel column chromatography (the ratio of solvents used: ethyl acetate/petroleum ether=5/95). White solid (81%), mp 238-240 C., Rf 0.24 (ethyl acetate/petroleum ether=5/95). IR (v, cm.sup.1, neat) 3898, 3851, 3819, 3800, 3749, 3742, 3731, 3687, 3674, 3668, 3646, 3627, 3565, 3099, 3019, 2930, 2844, 2798, 2588, 2216, 1912, 1595, 1567, 1473, 1406, 1382, 1330, 1282, 1263, 1206, 1120, 1098, 964, 953, 920, 813, 751, 670, 621, 603, 536, 524, 517, 506. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.46 (s, 1H), 7.83 (d, J=8.2 Hz, 1H), 7.21 (d, J=8.2 Hz, 1H), 6.76 (s, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 150.1 (Cq), 134.0 (Cq), 129.9 (CH), 121.2 (Cq), 119.7 (CH), 110.5 (CH), 81.9 (Cq). HRMS (+ESI) calculated for C.sub.7H.sub.5BrN.sub.2 (M+H+): 324.8655, found: 324.8652.

Example 10.15: 5-Bromo-2-iodo-1H-pyrrolo[2,3-b] pyridine 18k

(86) ##STR00195##

(87) The compound was prepared according to the sequence of procedures BI and D and purified by column chromatography on silicagel under pressure (the ratio of solvent used (methanol/dichloromethane=5/95), white solid (3% over 2 steps), mp 253-255 C., Rf 0.57 (methanol/dichloromethane=5/95). IR (v, cm.sup.1, neat) 2687, 1567, 1467, 1416, 1390, 1326, 1278, 1229, 924, 882, 805, 753, 683. (400 MHz, DMSO-d.sub.6, 20 C.) 12.46 (s, 1H), 8.19 (s, 1H), 8.11 (s, 1H), 6.69 (s, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 149.4 (Cq), 142.8 (CH), 128.8 (CH), 123.8 (Cq), 111.6 (Cq), 109.7 (CH), 83.8 (Cq). HRMS (+ESI) calculated for C.sub.7H.sub.5BrIN.sub.2 (M+H+): 322.8675, found: 322.8675.

Example 10.16 4-Chloro-2-iodo-1H-pyrrolo[2,3-b]pyridine 181

(88) ##STR00196##

(89) The compound was prepared according to the sequence of procedures BI and D and purified by precipitation from Et.sub.2O. White solid (58% over 2 steps), mp 231-233 C., IR (v, cm.sup.1, neat) 2722, 1602, 1568, 1480, 1428, 1387, 1326, 1307, 1265, 1183, 961, 905, 850, 801, 740, 664, 615, 522, 510, 508. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.60 (s, 1H), 8.10 (d, J=5.2 Hz, 1H), 7.16 (d, J=5.2 Hz, 1H), 6.75 (s, 1H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 151.1 (Cq), 143.2 (CH), 132.0 (Cq), 120.5 (Cq), 115.7 (CH), 107.5 (CH), 82.5 (Cq). HRMS (+ESI) calculated for C.sub.7H.sub.5ClIN.sub.2 (M+H+): 278.9181, found: 278.9184.

Example 10.17 tert-Butyl 2-iodo-1H-pyrrolo[2,3-b] pyridine-1-carboxylate 20a

(90) ##STR00197##

(91) The compound was prepared following procedure E and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). White solid (99%), mp 74-76 C., Rf=0.40 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3067, 2981, 1725, 1572, 1504, 1460, 1392, 1369, 1345, 1324, 1304, 1252, 1206, 1154, 1132, 1106, 1066, 1044, 912, 839, 805, 765, 665, 611, 589, 517, 511. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.36 (dd, J=4.8 Hz, J=1.6 Hz, 1H), 7.72 (dd, J=7.8 Hz, J=1.6 Hz, 1H), 7.08 (dd, J=7.8 Hz, J=4.8 Hz, 1H), 6.87 (s, 1H), 1.70 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 149.7 (Cq), 147.7 (Cq), 144.7 (CH), 127.3 (CH), 123.3 (Cq), 118.6 (CH), 118.0 (CH), 85.8 (Cq), 77.0 (Cq), 28.2 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.12H.sub.14IN.sub.2O.sub.2 (M+H+): 345.0095, found: 345.0094.

Example 10.18 tert-Butyl 2-iodo-1H-pyrrolo[3,2-c]pyridine-1-carboxylate 20b

(92) ##STR00198##

(93) The compound was prepared following procedure E and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80). white solid (88%), mp 82-84 C., Rf=0.19 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3041, 2983, 1733, 1592, 1504, 1479, 1447, 1432, 1394, 1367, 1331, 1316, 1271, 1254, 1178, 1150, 1056, 914, 844, 816, 768, 746, 644, 595, 544, 521, 505. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.66 (d, J=1.0 Hz, 1H), 8.27 (dd, J=5.9 Hz, J=1.0 Hz, 1H), 7.81 (dd, J=5.9 Hz, J=0.9 Hz, 1H), 6.92 (t, J=0.9 Hz, 1H), 1.62 (s, 9H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 148.6 (Cq), 144.0 (CH), 142.0 (CH), 141.6 (Cq), 127.6 (Cq), 120.0 (CH), 110.2 (CH), 86.5 (Cq), 28.3 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.12H.sub.14IN.sub.2O.sub.2 (M+H+): 345.0095, found: 345.0093.

Example 10.19 tert-Butyl 6-chloro-2-iodo-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 20e

(94) ##STR00199##

(95) The compound was prepared following procedure E and purified by flash column chromatography on silica gef (ethyl acetate/petroleum ether=1/99). White solid (99%), mp 81-83 C., Rf=0.16 (ethyl acetate/petroleum ether=1/99). IR (v, cm.sup.1, neat) 2986, 2973, 2929, 1746, 1592, 1568, 1493, 1474, 1457, 1436, 1392, 1367, 1352, 1311, 1276, 1251, 1157, 1127, 1101, 1068, 1037, 937, 844, 817, 772, 749, 738, 712, 640, 627, 589, 551, 517, 509, 503. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.69 (d, J=8.2 Hz, 1H), 7.15 (d, J=8.2 Hz, 1H), 6.91 (s, 1H), 1.72 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 147.8 (Cq), 147.6 (Cq), 146.1 (Cq), 129.4 (CH), 121.9 (Cq), 119.1 (CH), 117.6 (CH), 86.1 (Cq), 77.1 (Cq), 28.1 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.7H.sub.5ClIN.sub.2 (M+H+): 378.9705, found: 378.9704.

Example 10.20 tert-butyl 6-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 20j

(96) ##STR00200##

(97) The compound was prepared following procedure E and purified by column chromatography on silicagel under pressure (the ratio of solvents used: ethyl acetate/petroleum ether=1/99). Orange solid (81%), mp 69-71 C., Rf=0.38 (ethyl acetate/petroleum ether=1/99). IR (v, cm.sup.1, neat) 2972, 1746, 1588, 1561, 1489, 1431, 1390, 1367, 1349, 1308, 1275, 1250, 1156, 1136, 1096, 1065, 924, 843, 816, 771, 749, 734, 695, 517, 505, 503. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.60 (d, J=8.1 Hz, 1H), 7.29 (d, J=8.1 Hz, 1H), 6.89 (s, 1H), 1.72 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 148.0 (Cq), 147.7 (Cq), 136.3 (Cq), 129.1 (CH), 122.6 (Cq), 122.1 (CH), 117.7 (CH), 86.1 (Cq), 77.2 (Cq), 28.1 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.12H.sub.13BrIN.sub.2O.sub.2 (M+H+): 424.9180, found: 424.9178.

Example 11. Synthesis of Final Compounds and Analogue Protected Compounds

(98) The final products of type 22 were prepared by three different methods:

(99) either by coupling Sonogasbira from iodated derivatives protected by a benzenesulfonyl of type 3 and with a deprotection of the intermediate 21 (method 1);

(100) or by the Sonogashira coupling directly from unprotected iodated derivatives of type 18 (method 2); or by the Sonogashira coupling from iodated derivatives protected by a teri-butoxycarbonyl of type 20 and with a deprotection of the intermediate product 23 (Method 3)

(101) ##STR00201##

Example 11.1 N,N-Dimethyl-4-((1-(phenylsulfonyl)-1H-pyrrolo[2,3-b] pyridin-2-yl)ethynyl)aniline 21a

(102) ##STR00202##

(103) The compound was prepared according to procedure C2 and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). Yellow solid (62%), mp 185-187 C., Rf=0.18 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 2918, 2194, 1732, 1605, 1578, 1545, 1517, 1474, 1447, 1398, 1374, 1311, 1267, 1226, 1183, 1128, 1114, 1089, 1071, 1054, 1036, 997, 941, 871, 829, 811, 726, 683, 661, 626. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.47 (dd, J=4.8 Hz, J=1.6 Hz, 1H), 8.28-8.17 (m, 2H), 7.73 (dd, J=7.9 Hz, J=1.6 Hz, 1H), 7.57-7.48 (m, 3H), 7.47-7.37 (m, 2H), 7.16 (dd, J=7.9 Hz, J=4.8 Hz, 1H), 6.75 (s, 1H), 6.73-6.63 (m, 2H), 3.02 (s, 6H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 150.7 (Cq), 148.3 (CH), 145.3 (Cq), 139.2 (Cq), 133.8 (CH), 132.9 (2CH), 129.0 (2CH), 128.6 (CH), 127.8 (2CH), 122.6 (Cq), 121.8 (Cq), 119.4 (CH), 111.8 (2CH), 111.5 (CH), 108.7 (Cq), 99.7 (Cq), 78.6 (Cq), 40.15 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.23H.sub.20N.sub.3O.sub.2S (M+H+): 402.1271, found: 402.1274.

Example 11.2 N,N-Dimethyl-4-((1-(phenylsulfonyl)-1H-pyrrolo[3,2-b] pyridin-2-yl)ethynyl)aniline 21c

(104) ##STR00203##

(105) The compound was prepared according to procedure C2 and purified by flash column chromatography on silicagel (etliyle acetate/petroleum ether=30/70). Brown oil (98%), Rf.sub.0.22 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 2924, 2200, 1733, 1605, 1566, 1549, 1516, 1446, 1405, 1367, 1268, 1225, 1169, 1127, 1089, 1043, 945, 816, 727, 685, 583, 559, 506, 503. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.56 (dd, J=4.7 Hz, J=1.1 Hz, 1H), 8.51 (d, J=8.4 Hz, 1H), 8.01-7.96 (m, 2H), 7.60-7.51 (m, 3H), 7.43 (m, 2H), 7.29 (m, 1H), 7.04 (m, 1H), 6.72 (d, J=9.0 Hz, 2H), 3.06 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 150.8 (Cq), 147.3 (Cq), 146.9 (CH), 138.4 (Cq), 134.2 (CH), 133.0 (2CH), 130.3 (Cq), 129.2 (2CH), 127.2 (2CH), 125.3 (Cq), 121.7 (CH), 119.5 (CH), 115.4 (CH), 111.8 (2CH), 108.2 (Cq), 101.3 (Cq), 78.2 (Cq), 40.1 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.23H.sub.20N.sub.3O.sub.2S (M+H+): 402.1271, found: 402.1271.

Example 11.3 N,N-Dimthyl-4-((1-(phenylsulfonyl)-1H-pyrrolo[2,3-c] pyridin-2-yl)ethynyl)aniline 21d

(106) ##STR00204##

(107) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=30/70). Brown solid (80%), mp 168-170 C., Rf=0.34 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3058, 2205, 1679, 1603, 1536, 1446, 1428, 1351, 1272, 1224, 1183, 1123, 1088, 1050, 836, 817, 729, 680, 654, 574, 556, 512. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 9.55 (s, 1H), 8.43 (d, J=5.1 Hz, 1H), 8.12-7.96 (m, 2H), 7.64-7.50 (m, 3H), 7.47-7.37 (m, 3H), 6.79 (s, 1H), 6.72 (d, J=8.9 Hz, 2H), 3.05 (s, 6H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 150.9 (Cq), 142.9 (Cq), 138.3 (Cq), 136.7 (CH), 134.8 (Cq), 134.2 (CH), 133.1 (2CH), 129.3 (2CH), 127.3 (2CH), 125.2 (Cq), 114.9 (CH), 113.2 (CH), 111.7 (2CH), 107.9 (Cq), 101.0 (Cq), 78.0 (Cq), 40.1 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.23H.sub.20N.sub.3O.sub.2S (M+H+): 402.1271, found: 402.1273.

Example 11.4 4-((6-chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 21e

(108) ##STR00205##

(109) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=5/95). Brown solid (99%), mp 195-197 C., Rf=0.41 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 2204, 1608, 1567, 1544, 1439, 1379, 1361, 1312, 1279, 1246, 1180, 1111, 1093, 1042, 812, 736, 686, 617, 577, 561, 515, 506, 503. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.22 (m, 2H), 7.63 (dd, J=8.2 Hz, J=1.1 Hz, 1H), 7.57-7.38 (m, 5H), 7.13 (dd, J=8.2 Hz, J=1.1 Hz, 1H), 6.74-6.55 (m, 3H), 2.99 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 6 150.7 (Cq), 146.7 (Cq), 146.6 (Cq), 138.8 (Cq), 134.1 (CH), 133.0 (2CH), 130.5 (CH), 129.0 (2CH), 128.2 (2CH), 123.0 (Cq), 120.1 (Cq), 119.9 (CH), 111.8 (2CH), 110.7 (CH), 108.6 (Cq), 100.0 (Cq), 78.3 (Cq), 40.2 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.23H.sub.19ClN.sub.3O.sub.2S (M+H+): 436.0881, found: 436.0881.

Example 11.5 3-((1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 21f

(110) ##STR00206##

(111) The compound was prepared according to procedure C and puriffe by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). Brown solid (94%), mp 156-158 C., Rf=0.32 (ethyl acetate/petroleum ether=10:90). IR (v, cm.sup.1, neat) 3431, 3325, 3228, 3061, 2360, 2210, 1637, 1598, 1575, 1486, 1447, 1394, 1377, 1333, 1262, 1176, 1127, 1088, 1033, 993, 916, 860, 822, 782, 764, 724, 683, 570, 553, 509. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.52 (dd, J=4.8 Hz, J=1.6 Hz, 1H), 8.25 (dd, J=8.4 Hz, J=1.4 Hz, 2H), 7.80 (dd, J=7.9 Hz, J=1.6 Hz, 1H), 7.58 (m, 1H), 7.48 (dd, J=8.5 Hz, J=7.1 Hz, 2H), 7.21 (ddd, J=7.8 Hz, J=6.3 Hz, J=1.4 Hz, 2H), 7.09 (dt, J=7.7 Hz, J=1.2 Hz, 1H), 7.02 (t, J=1.9 Hz, 1H), 6.87 (s, 1H), 6.76 (ddd, J=7.9 Hz, J=2.4 Hz, J=1.0 Hz, 1H), 3.79 (s, 2H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 148.5 (Cq), 146.6 (Cq), 146.1 (CH), 139.2 (Cq), 134.1 (CH), 129.6 (CH), 129.2 (2CH), 129.1 (CH), 128.0 (2CH), 123.2 (Cq), 122.1 (CH), 121.9 (Cq), 121.6 (Cq), 119.7 (CH), 117.8 (CH), 116.3 (CH), 113.1 (CH), 98.2 (Cq), 79.7 (Cq). HRMS (+ESI) calculated for C.sub.21H.sub.16N.sub.3O.sub.2S (M+H+): 374.0958, found: 374.0957.

Example 11.6 4-((1H-Pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 22a

(112) ##STR00207##

(113) The compound was prepared following procedure E and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=15/85). Yellow solid (92%), mp 229-231 C., Rf=0.36 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3055, 2886, 2796, 2198, 1603, 1584, 1538, 1509, 1433, 1405, 1354, 1326, 1281, 1223, 1186, 1165, 1118, 1061, 976, 945, 918, 807, 763, 699, 645, 625. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.07 (s, 1H), 8.20 (m, 1H), 7.92 (dd, J=7.8 Hz, J=1.7 Hz, 1H), 7.39 (d, J=8.4 Hz, 2H), 7.08 (dd, J=7.8 Hz, J=4.6 Hz, 1H), 6.84-6.46 (m, 3H), 2.97 (s, 6H). .sup.13C NMR (100 MHz, DMSO-d.sub.6, 20 C.) 150.8 (Cq), 148.8 (Cq), 144.3 (CH), 132.9 (2CH), 128.4 (CH), 120.6 (Cq), 120.2 (Cq), 116.6 (CH), 112.4 (2CH), 108.0 (Cq), 105.4 (CH), 94.9 (Cq), 80.5 (Cq), 40.1 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.17H.sub.16N.sub.3 (M+H+): 262.1339, found: 262.1340.

Example 11.7 4-((1H-Pyrrolo[2,3-c]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 22b

(114) ##STR00208##

(115) The compound was prepared according to procedure D and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80). Yellow solid (88%), mp 242-244 C., Rf=0.27 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 2669, 2207, 1609, 1573, 1535, 1361, 1303, 1224, 1187, 906, 811, 598, 515. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.08 (large s, 1H), 8.67 (s, 1H), 8.10 (d, J=5.5 Hz, 1H), 7.49 (dd, J=5.5 Hz, J=1.0 Hz, 1H), 7.45-7.36 (m, 2H), 6.79-6.71 (m, 3H), 2.98 (s, 6H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 151.0 (Cq), 138.6 (CH), 134.4 (CH), 133.0 (2CH), 132.2 (Cq), 123.6 (Cq), 112.4 (2CH), 107.5 (Cq), 105.8 (CH), 95.1 (Cq), 80.1 (Cq), 40.1 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.17H.sub.16N.sub.3 (M+H+): 262.1339, found: 262.1338.

Example 11.8 4-((1H-Pyrrolo[3,2-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 22c

(116) ##STR00209##

(117) The compound was prepared following procedure E and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=30/70). Orange solid (87%), mp 191-193 C., Rf=0.24 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3064, 2889, 2806, 2703, 2199, 1673, 1606, 1570, 1537, 1512, 1406, 1355, 1286, 1223, 1186, 1122, 943, 913, 814, 778, 623, 558, 514. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 11.82 (s, 1H), 8.35 (dd, J=4.6 Hz, J=1.2 Hz, 1H), 7.69 (d, J=8.1 Hz, 1H), 7.40 (t, J=8.9 Hz, 2H), 7.14 (dd, J=8.2 Hz, J=4.6 Hz, 1H), 6.81 (d, J=0.9 Hz, 1H), 6.75 (d, J=8.9 Hz, 2H), 2.97 (s, 6H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 150.9 (Cq), 145.9 (Cq), 143.8 (CH), 132.9 (2CH), 129.7 (Cq), 123.2 (Cq), 118.4 (CH), 117.8 (CH), 112.4 (2CH), 107.8 (Cq), 106.8 (CH), 95.4 (Cq), 80.4 (Cq), 40.1 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.17H.sub.16N.sub.3 (M+H+): 262.1339, found: 262.1342.

Example 11.9 4-((1H-Pyrrolo[3,2-c]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 22d

(118) ##STR00210##

(119) The compound was prepared according to procedure F and purified by flash column chromatography on silicagel (ethyl acetate). Orange solid (47%), mp 250-252 C., Rf=0.22 (ethyl acetate). IR (v, cm.sup.1, neat) 2899, 2623, 2203, 1605, 1543, 1517, 1369, 1292, 1233, 1182, 814, 762, 519, 506. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 11.99 (s, 1H), 8.80 (s, 1H), 8.19 (d, J=5.7 Hz, 1H), 7.43-7.36 (m, 2H), 7.29 (dt, J=5.8 Hz, J=1.0 Hz, 1H), 6.84 (s, 1H), 6.78-6.68 (m, 2H), 2.97 (s, 6H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 150.86, 143.51 (CH), 141.58 (CH), 139.88, 132.91 (2CH), 125.03, 121.04, 112.37 (2CH), 107.83, 106.77 (CH), 105.86 (CH), 94.44, 80.12, 40.12 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.17H.sub.16N.sub.3 (M+H+): 262.1339, found: 262.1340.

Example 11.10 4-((6-Chloro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 22e

(120) ##STR00211##

(121) The compound was prepared according to procedure D (32%) or by procedure F (35%) and purified by flash chromatography column on silicagel (ethyl acetate/petroleum ether=5/95). Yellow solid. mp 241-243 C., Rf=0.32 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 2895, 2121, 1600, 1514, 1440, 1360, 1224, 1160, 942, 815, 510. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.27 (s, 1H), 7.93 (d, J=8.2 Hz, 1H), 7.42-7.25 (m, 2H), 7.09 (d, J=8.2 Hz, 1H), 6.75-6.64 (m, 3H), 2.92 (s, 6H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 150.9 (Cq), 147.5 (Cq), 144.6 (Cq), 132.9 (2CH), 131.5 (CH), 121.2 (Cq), 119.2 (Cq), 116.5 (CH), 112.4 (2CH), 107.7 (Cq), 105.7 (CH), 95.4 (Cq), 80.1 (Cq), 40.1 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.17H.sub.15ClN.sub.3 (M+H+): 296.0949, found: 296.0946.

Example 11.11 4-((6-Fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 22f

(122) ##STR00212##

(123) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). Yellow solid (62%), mp 232-234 C., Rf=0.33 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3157, 3072, 2893, 2205, 1605, 1541, 1511, 1432, 1273, 1224, 1183, 809, 763, 507. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.23 (s, 1H), 8.08 (t, J=8.2 Hz, 1H), 7.38 (d, J=8.3 Hz, 2H), 6.84 (d, J=8.3 Hz, 1H), 6.78-6.57 (m, 3H), 2.97 (s, 6H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 160.6 (d, J=233.8 Hz, Cq), 150.8 (Cq), 145.2 (d, J=19.3 Hz, Cq), 133.7 (d, J=9.5 Hz, CH), 132.9 (2CH), 120.2 (d, J=4.5 Hz, Cq), 118.1 (d, J=2.7 Hz, Cq), 112.4 (2CH), 107.9 (Cq), 105.9 (CH), 102.04 (d, J=38.8 Hz, CH), 94.7 (Cq), 80.1 (Cq), 40.1 (2CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 74.40. HRMS (+ESI) calculated for C.sub.17H.sub.15FN.sub.3 (M+H+): 280.1245, found: 280.1243.

Example 11.12 4-((5-Fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 22 g

(124) ##STR00213##

(125) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=15/85). Yellow solid (68%), mp 255-257 C., Rf=0.25 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3120, 2987, 2897, 2801, 2360, 2209, 1609, 1583, 1541, 1503, 1447, 1399, 1362, 1345, 1293, 1230, 1189, 1151, 1109, 1066, 976, 944, 875, 817, 761, 559, 519, 509. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.23 (s, 1H), 8.20 (m, 1H), 7.80 (dd, J=9.5 Hz, J=2.8 Hz, 1H), 7.39 (d, J=8.4 Hz, 2H), 6.75 (d, J=8.4 Hz, 2H), 6.67 (m, 1H), 2.98 (s, 6H). .sup.13C NMR (101 MHz, DMSO, 20 C.) 155.7 (d, J=239.5 Hz, Cq), 150.9 (Cq), 145.6 (Cq), 132.9 (2CH), 132.4 (d, J=29.0 Hz, CH), 122.9 (Cq), 120.3 (d, J=7.5 Hz, Cq), 113.7 (d, J=20.7 Hz, CH), 112.4 (2CH), 107.7 (Cq), 105.4 (d, J=4.5 Hz, CH), 95.5 (Cq), 80.2 (Cq), 40.1 (2CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 138.76. HRMS (+ESI) calculated for C.sub.17H.sub.15FN.sub.3 (M+H+): 280.1245, found: 280.1243.

Example 11.13 4-((4-Fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 22 h

(126) ##STR00214##

(127) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80). White solid (73%), mp 248-250 C., Rf=0.31 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3066, 2900, 2803, 2359, 2201, 1604, 1540, 1510, 1441, 1362, 1345, 1326, 1299, 1274, 1250, 1231, 1185, 1170, 1078, 1058, 980, 946, 881, 796, 753, 618, 594, 530, 510. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.45 (s, 1H), 8.25 (dd, J=8.2 Hz, J=5.3 Hz, 1H), 7.40 (d, J=8.3 Hz, 2H), 6.98 (dd, J=10.3 Hz, J=5.4 Hz, 1H), 6.82-6.67 (m, 3H), 2.97 (s, 6H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 161.2 (d, J=260.9 Hz, Cq), 152.0 (d, J=11.4 Hz, Cq), 150.92 (Cq), 146.3 (d, J=6.1 Hz, CH), 133.0 (2CH), 120.9 (Cq), 112.4 (2CH), 109.2 (d, J=18.1 Hz, Cq), 107.6 (Cq), 102.9 (d, J=14.6 Hz, CH), 100.9 (CH), 95.2 (Cq), 79.8 (Cq), 40.1 (2CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 111.96. HRMS (+ESI) calculated for C.sub.17H.sub.15FN.sub.3 (M+H+): 280.1245, found: 280.1246.

Example 11.14 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-methylaniline 22i

(128) ##STR00215##

(129) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80). Beige solid (87%), mp 208-210 C., Rf=0.19 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3409, 3056, 2195, 1602, 1532, 1509, 1478, 1431, 1406, 1358, 1324, 1282, 1177, 1157, 1123, 917, 823, 802, 764, 625, 550, 542, 527, 519, 512, 506. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.04 (s, 1H), 8.23 (d, J=3.6 Hz, 1H), 7.91 (d, J=7.6 Hz, 1H), 7.31 (d, J=8.5 Hz, 2H), 7.07 (dd, J=7.7 Hz, J=3.6 Hz, 1H), 6.69 (d, J=1.1 Hz, 1H), 6.57 (d, J=8.5 Hz, 2H), 6.23 (d, J=4.9 Hz, 1H), 2.72 (d, J=4.9 Hz, 3H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 150.9 (Cq), 148.7 (Cq), 144.2 (CH), 133.0 (2CH), 128.3 (CH), 120.7 (Cq), 120.2 (Cq), 116.6 (CH), 112.0 (2CH), 107.6 (Cq), 105.3 (CH), 95.2 (Cq), 80.0 (Cq), 29.7 (CH.sub.3). HRMS (+ESI) calculated for C.sub.16H.sub.14N.sub.3 (M+H+): 248.1182, found: 248.1183.

Example 11.15 3-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 22j

(130) ##STR00216##

(131) The compound was prepared following procedure E and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=30/70). White solid (67%), mp 196-198 C., Rf=0.14 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3465, 3373, 3201, 3075, 3053, 2975, 2895, 2817, 2746, 1601, 1579, 1535, 1488, 1448, 1430, 1407, 1361, 1312, 1283, 1190, 1169, 1115, 992, 916, 852, 801, 767, 735, 681, 634, 621, 570, 526, 513, 503. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.17 (s, 1H), 8.28 (d, J=3.8 Hz, 1H), 7.95 (d, J=7.7 Hz, 1H), 7.11 (d, J=7.8 Hz, 2H), 6.91-6.45 (m, 4H), 5.31 (s, 2H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 149.4 (Cq), 148.8 (Cq), 144.7 (CH), 129.8 (CH), 128.8 (CH), 122.3 (Cq), 20.0 (Cq), 119.7 (Cq), 119.1 (CH), 116.8 (CH), 116.4 (CH), 115.4 (CH), 106.4 (CH), 94.2 (Cq), 81.2 (Cq). HRMS (+ESI) calculated for C.sub.15H.sub.12N.sub.3 (M+H+): 234.1026, found: 234.1025.

Example 11.16 2-((3-fluorophenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 22k

(132) ##STR00217##

(133) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80). White solid (64%), mp 220-222 C., Rf=0.24 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3056, 2817, 1607, 1577, 1481, 1434, 1406, 1360, 1283, 1174, 1112, 917, 807, 767, 676, 572, 517, 507. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.26 (s, 1H), 8.30 (dd, J=4.6 Hz, J=1.4 Hz, 1H), 7.97 (dd, J=7.9 Hz, J=1.4 Hz, 1H), 7.51 (dd, J=14.1 Hz, J=7.7 Hz, 1H), 7.46-7.39 (m, 2H), 7.37-7.28 (m, 1H), 7.11 (dd, J=7.9 Hz, J=4.7 Hz, 1H), 6.86 (s, 1H). .sup.13C-NMR (101 MHz, DMSO-d.sub.6, 20 C.) 162.4 (d, J=244.9 Hz), 148.8 (Cq), 145.2 (CH), 131.5 (d, J=8.9 Hz, CH), 129.1 (CH), 128.2 (d, J=2.9 Hz, CH), 124.1 (d, J=9.7 Hz, Cq), 119.9 (Cq), 118.8 (Cq), 118.3 (d, J=23.1 Hz, CH), 117.0 (d, J=21.1 Hz, CH), 116.9 (CH), 107.3 (CH), 91.9 (d, J=3.4 Hz, Cq), 83.6 (Cq). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 112.1.

(134) HRMS (+ESI) calculated for C.sub.15H.sub.10FN.sub.2 (M+H+): 237.0823, found: 237.0821.

Example 11.17 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 221

(135) ##STR00218##

(136) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=40/60). Yellow solid (87%), mp 244-246 C., Rf=0.19 (Ethyl acetate/petroleum ether=40/60). IR (v, cm.sup.1, neat) 3471, 3375, 3052, 2879, 2199, 1616, 1603, 1585, 1538, 1503, 1405, 1356, 1299, 1278, 1175, 917, 818, 761, 626, 568, 514, 511, 507, 503. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.04 (s, 1H), 8.23 (dd, J=4.6 Hz, J=1.4 Hz, 1H), 7.90 (m, 1H), 7.24 (d, J=8.5 Hz, 2H), 7.07 (dd, J=7.9 Hz, J=4.7 Hz, 1H), 6.68 (d, J=1.7 Hz, 1H), 6.59 (d, J=8.5 Hz, 2H), 5.65 (s, 2H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 150.3 (Cq), 148.7 (Cq), 144.2 (CH), 133.0 (2CH), 128.3 (CH), 120.6 (Cq), 120.1 (Cq), 116.6 (CH), 114.1 (2CH), 107.7 (Cq), 105.2 (CH), 95.2 (Cq), 79.7 (Cq). HRMS (+ESI) calculated for C.sub.15H.sub.12N.sub.3 (M+H+): 234.1026, found: 234.1025.

Example 11.18 2-((4-methoxyphenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 22m

(137) ##STR00219##

(138) The compound was prepared according to Procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=30/70). Yellow solid (83%), mp 193-195 C., Rf=0.26 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3054, 2976, 2832, 1600, 1583, 1536, 1501, 1436, 1404, 1358, 1280, 1242, 1171, 1107, 1027, 917, 812, 768, 723, 625, 562, 537, 507, 503. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.15 (s, 1H), 8.27 (dd, J=4.7 Hz, J=1.4 Hz, 1H), 7.95 (dd, J=7.9 Hz, J=1.2 Hz, 1H), 7.53 (d, J=8.8 Hz, 2H), 7.09 (dd, J=7.9 Hz, J=4.7 Hz, 1H), 7.03 (d, J=8.8 Hz, 2H), 6.78 (d, J=1.6 Hz, 1H), 3.82 (s, 3H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 160.3 (Cq), 148.8 (Cq), 144.7 (CH), 133.4 (2CH), 128.7 (CH), 120.0 (Cq), 119.8 (Cq), 116.8 (CH), 115.0 (2CH), 114.0 (Cq), 106.2 (CH), 93.3 (Cq), 81.3 (Cq), 55.8 (CH.sub.3). HRMS (+ESI) calculated for C.sub.16H.sub.13N.sub.20 (M+H+): 249.1022, found: 249.1021.

Example 11.19 4-((6-fluoro-1-methyl-1H-pyrrolo[2,3-b] pyridin-2-yl)ethynyl)-N,N-dimethylaniline 22n

(139) ##STR00220##

(140) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=2/98). Greyish solid (72%), mp 194-196 C., Rf=0.24 (ethyl acetate/petroleum ether=4/96). IR (v, cm.sup.1, neat) 2896, 2202, 1606, 1577, 1539, 1505, 1445, 1406, 1358, 1316, 1278, 1230, 1191, 1092, 985, 947, 804, 760, 581, 517, 506, 502. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.90 (t, J=8.0 Hz, 1H), 7.46 (d, J=8.1 Hz, 2H), 6.84-6.65 (m, 4H), 3.90 (s, 3H), 3.04 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 160.9 (d, J=237.3 Hz, Cq), 150.6 (Cq), 144.8 (d, J=18.0 Hz, Cq), 132.8 (2CH), 132.8 (CH), 123.5 (d, J=4.8 Hz, Cq), 117.6 (d, J=2.7 Hz, Cq), 111.9 (2CH), 108.8 (Cq), 104.5 (CH), 101.7 (d, J=38.8 Hz, CH), 97.6 (Cq), 78.3 (Cq), 40.3 (2CH.sub.3), 29.5 (CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) 74.2. HRMS (+ESI) calculated for C.sub.18H.sub.17FN.sub.3 (M+H+): 294.1401, found: 294.1401.

Example 11.20 tert-Butyl-2-((4-(dimethylamino)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 23a

(141) ##STR00221##

(142) The compound was prepared according to procedure C2 and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=15/85). Yellow solid (91%), mp 188-190 C., Rf=0.39 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3064, 2982, 2906, 2194, 1738, 1604, 1572, 1542, 1515, 1444, 1399, 1363, 1253, 1142, 1114, 1089, 974, 942, 840, 826, 813, 788, 773, 751, 697, 517, 504. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.53 (dd, J=4.8 Hz, J=1.6 Hz, 1H), 7.83 (dd, J=7.8 Hz, J=1.6 Hz, 1H), 7.50-7.39 (m, 2H), 7.19 (dd, J=7.8 Hz, J=4.8 Hz, 1H), 6.82 (s, 1H), 6.76-6.62 (m, 2H), 3.03 (s, 6H), 1.71 (s, 9H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 150.4 (Cq), 148.6 (Cq), 148.1 (Cq), 145.7 (CH), 132.7 (2CH), 128.3 (CH), 122.0 (Cq), 121.6 (Cq), 118.8 (CH), 111.8 (2CH), 111.6 (CH), 109.2 (Cq), 97.1 (Cq), 84.6 (Cq), 79.7 (Cq), 40.1 (2CH.sub.3), 28.2 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.22H.sub.24N.sub.3O.sub.2 (M+H+): 362.1863, found: 362.1862.

Example 11.21 tert-Butyl-2-((4-(dimethylamino)phenyl)ethynyl)-1H-pyrrolo[3,2-c]pyridine-1-carboxylate 23b

(143) ##STR00222##

(144) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). Yellow solid (99%), mp 162-164 C., Rf=0.44 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 2983, 2205, 1733, 1604, 1549, 1517, 1456, 1338, 1317, 1247, 1149, 1092, 814, 507. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.82 (s, 1H), 8.45 (d, J=5.8 Hz, 1H), 8.00 (d, J=5.8 Hz, 1H), 7.43 (d, J=7.9 Hz, 2H), 6.93 (s, 1H), 6.67 (d, J=8.0 Hz, 2H), 3.00 (s, 6H), 1.69 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 150.4 (Cq), 149.1 (Cq), 144.6 (CH), 143.2 (CH), 140.3 (Cq), 132.8 (2CH), 125.4 (Cq), 122.8 (Cq), 112.9 (CH), 111.7 (2CH), 110.3 (CH), 109.1 (Cq), 97.3 (Cq), 85.1 (Cq), 79.3 (Cq), 40.1 (2CH.sub.3), 28.2 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.22H.sub.24N.sub.3O.sub.2 (M+H+): 362.1863, found: 362.1862.

Example 11.22 tert-Butyl-6-chloro-2-((4-(dimethylamino)phenyl)ethynyl)-1H-pyrrolo[2,3-b] pyridine-1-carboxylate 23e

(145) ##STR00223##

(146) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). Yellow solid (93%), mp 160-162 C., Rf=0.38 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 2923, 2853, 2196, 1740, 1611, 1567, 1546, 1517, 1439, 1397, 1368, 1334, 1306, 1268, 1245, 1186, 1152, 1140, 1110, 944, 881, 842, 813, 770, 744, 722, 602, 529. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.71 (d, J=8.3 Hz, 1H), 7.40 (d, J=9.0 Hz, 2H), 7.17 (d, J=8.2 Hz, 1H), 6.75 (s, 1H), 6.64 (d, J=9.0 Hz, 2H), 2.99 (s, 6H), 1.67 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 150.5 (Cq), 147.6 (Cq), 147.0 (Cq), 146.9 (Cq), 132.8 (2CH), 130.3 (CH), 122.6 (Cq), 120.1 (Cq), 119.3 (CH), 111.7 (2CH), 110.9 (CH), 108.9 (Cq), 97.8 (Cq), 85.0 (Cq), 79.3 (Cq), 40.1 (2CH.sub.3), 28.2 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.22H.sub.23ClN.sub.3O.sub.2 (M+H+): 396.1473, found: 396.1474.

Example 11.23 tert-Butyl-2-((4-(methylamino)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 23i

(147) ##STR00224##

(148) The compound was prepared according to procedure C and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80). Yellow solid (91%), mp 166-168 C., Rf=0.34 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3368, 3066, 2983, 2936, 2815, 2198, 1742, 1607, 1575, 1545, 1521, 1472, 1404, 1367, 1339, 1308, 1251, 1177, 1154, 1112, 1087, 876, 847, 826, 772, 640, 599, 561, 532, 515. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.53 (d, J=3.9 Hz, 1H), 7.83 (d, J=7.7 Hz, 1H), 7.40 (d, J=8.3 Hz, 2H), 7.19 (dd, J=7.5 Hz, J=4.9 Hz, 1H), 6.81 (s, 1H), 6.59 (d, J=8.3 Hz, 2H), 4.02 (1s, 1H), 2.89 (s, 3H), 1.70 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 149.6 (Cq), 148.6 (Cq), 148.1 (Cq), 145.7 (CH), 132.9 (2CH), 128.3 (CH), 122.0 (Cq), 121.6 (Cq), 118.8 (CH), 112.0 (2CH), 111.6 (CH), 110.2 (Cq), 97.0 (Cq), 84.6 (Cq), 79.5 (Cq), 30.3 (CH.sub.3), 28.2 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.21H.sub.22N.sub.3O.sub.2 (M+H+): 348.1707, found: 348.1705.

Example 11.24 tert-butyl-6-bromo-2-((4-(dimethylamino)phenyl)ethynyl)-1H-pyrrolo[2,3-b] pyridine-1-carboxylate 23j

(149) ##STR00225##

(150) The compound was prepared according to procedure C and purified by column chromatography on silicagel under pressure (the ratio of solvents used: ethyl acetate/dichloromethane/petroleum ether=7/3/90). Yellow solid (68%), mp 170-172 C., Rf=0.27 (ethyl acetate/dichloromethane/petroleum ether=3/7/90). IR (v, cm.sup.1, neat) 2983, 2200, 1752, 1606, 1561, 1542, 1434, 1394, 1367, 1353, 1332, 1306, 1240, 1153, 1137, 1103, 875, 832, 815, 802, 768, 518, 502. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.64 (d, J=8.2 Hz, 1H), 7.46-7.39 (m, 2H), 7.33 (d, J=8.2 Hz, 1H), 6.75 (s, 1H), 6.70-6.57 (m, 2H), 3.01 (s, 6H), 1.69 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 150.5 (Cq), 147.6 (Cq), 147.2 (Cq), 137.0 (Cq), 132.8 (2CH), 130.0 (CH), 122.9 (CH), 122.5 (Cq), 120.3 (Cq), 111.7 (2CH), 110.9 (CH), 108.9 (Cq), 98.0 (Cq), 84.9 (Cq), 79.3 (Cq), 40.1 (2CH.sub.3), 28.2 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.22H.sub.23BrN.sub.3O.sub.2 (M+H+): 440.0968, found: 440.0967.

Example 12. Synthesis of Final Compounds Functionalized at the C-6 Position of 7-Azaindole

(151) to prepare the functionalized compounds on position 6, a Suzuki coupling was carried out starting from compound 23e to give compound 24 which then deprotected according to procedure F

(152) ##STR00226##

Example 12.1 tert-Butyl 2-((4-(dimethylamino)phenyl)ethynyl)-6-(thiophen-2-yl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 24a

(153) ##STR00227##

(154) The compound was prepared according to procedure G2 and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=5/95). Yellow solid (37%), mp 173-175 C., Rf=0.42 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 2927, 2197, 1744, 1593, 1365, 1258, 1154, 829, 696, 508. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.79 (d, J=8.1 Hz, 1H), 7.64 (m, 1H), 7.59 (d, J=8.2 Hz, 1H), 7.48 (d, J=7.7 Hz, 2H), 7.38 (d, J=4.8 Hz, 1H), 7.12 (m, 1H), 6.79 (s, 1H), 6.70 (d, J=7.7 Hz, 2H), 3.03 (s, 6H), 1.80 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 150.4 (Cq), 148.4 (Cq), 147.8 (Cq), 146.0 (Cq), 132.9 (2CH), 128.6 (CH), 127.9 (CH), 127.0 (CH), 126.4 (Cq), 124.3 (CH), 122.4 (Cq), 120.4 (Cq), 114.6 (CH), 111.8 (2CH), 111.2 (CH), 109.4 (Cq), 97.9 (Cq), 84.3 (Cq), 79.9 (Cq), 40.2 (2CH.sub.3), 28.4 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.26H.sub.26N.sub.3O.sub.2S (M+H+): 444.1740, found: 444.1742.

Example 12.2 N,N-Dimethyl-4-((6-(thiophen-2-yl)-1H-pyrrol[2,3-b]pyridin-2-yl)ethynyl)aniline 25a

(155) ##STR00228##

(156) The compound was prepared according to procedure F and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). Yellow solid (38%), mp 231-233 C., Rf=0.55 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3066, 1597, 1535, 1416, 1278, 821, 705. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.16 (s, 1H), 7.95 (d, J=8.3 Hz, 1H), 7.77 (dd, J=3.7 Hz, J=1.1 Hz, 1H), 7.67 (d, J=8.3 Hz, 1H), 7.58 (dd, J=5.1 Hz, J=1.1 Hz, 1H), 7.39 (d, J=8.9 Hz, 2H), 7.16 (dd, J=5.1 Hz, J=3.7 Hz, 1H), 6.75 (d, J=8.9 Hz, 2H), 6.71 (d, J=2.0 Hz, 1H), 2.98 (s, 6H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 150.8 (Cq), 148.3 (Cq), 147.0 (Cq), 146.1 (Cq), 132.6 (2CH), 129.2 (CH), 128.8 (CH), 127.7 (CH), 124.9 (CH), 120.9 (Cq), 119.4 (Cq), 112.8 (CH), 112.4 (2CH), 108.0 (Cq), 105.9 (CH), 95.3 (Cq), 80.6 (Cq), 40.1 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.21H.sub.18N.sub.3S (M+H+): 344.1216, found: 344.1216.

Example 12.3 tert-butyl 2-((4-(dimethylamino)phenyl)ethynyl)-6-(thiophen-3-yl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 24b

(157) ##STR00229##

(158) The compound was prepared according to procedure GI and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). Yellow solid (57%), mp 163-165 C., Rf=0.29 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 1743, 1607, 1257, 1154, 769, 507. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.98 (dd, J=3.0 Hz, J=1.2 Hz, 1H), 7.86-7.78 (m, 2H), 7.57 (d, J=8.2 Hz, 1H), 7.52-7.44 (m, 2H), 7.41 (dd, J=5.1 Hz, J=3.0 Hz, 1H), 6.81 (s, 1H), 6.74-6.65 (m, 2H), 3.03 (s, 6H), 1.77 (s, 9H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 150.3 (Cq), 149.4 (Cq), 148.3 (Cq), 148.2 (Cq), 143.0 (Cq), 132.8 (2CH), 128.7 (CH), 126.6 (CH), 125.9 (CH), 123.0 (CH), 122.3 (Cq), 120.1 (Cq), 115.9 (CH), 111.8 (2CH), 111.4 (CH), 109.4 (Cq), 97.6 (Cq), 84.1 (Cq), 80.0 (Cq), 40.2 (2CH.sub.3), 28.4 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.26H.sub.26N.sub.3O.sub.2S (M+H+): 444.1740, found: 444.1738.

Example 12.4 N,N-Dimethyl-4-((6-(thiophen-3-yl)-1H-pyrrol[2,3-b]pyridin-2-yl)ethynyl)aniline 25b

(159) ##STR00230##

(160) The compound was prepared according to procedure F and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=3/97). Yellow solid (66%), mp 220-222 C., Rf=0.46 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3103, 2211, 1768, 1596, 1536, 1501, 1422, 1328, 1269, 1163, 1138, 1054, 935, 864, 821, 769, 691, 603, 564, 520. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.09 (s, 1H), 8.11 (d, J=1.7 Hz, 1H), 7.95 (d, J=8.2 Hz, 1H), 7.79 (d, J=4.1 Hz, 1H), 7.63 (m, 2H), 7.39 (d, J=8.8 Hz, 2H), 6.75 (d, J=8.9 Hz, 2H), 6.71 (d, J=1.8 Hz, 1H), 2.98 (s, 6H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 150.8 (Cq), 148.6 (Cq), 148.1 (Cq), 143.2 (Cq), 132.9 (2CH), 129.2 (CH), 127.2 (CH), 126.9 (CH), 123.2 (CH), 120.8 (Cq), 119.1 (Cq), 114.2 (CH), 112.4 (2CH), 108.1 (Cq), 105.7 (CH), 95.1 (Cq), 80.7 (Cq), 40.1 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.21H.sub.18N.sub.3S (M+H+): 344.1216, found: 344.1216.

Example 12.5 tert-Butyl-2-((4-(dimethylamino)phenyl)ethynyl)-6-(6-fluoropyridin-3-yl)-1H-pyrrolo[2,3-b] pyridine-1-carboxylate 24c

(161) ##STR00231##

(162) The compound was prepared according to procedure GI and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). Yellow solid (46%), mp 168-170 C., Rf=0.49 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 2925, 2196, 1740, 1612, 1567, 1546, 1439, 1398, 1369, 1335, 1306, 1269, 1245, 1154, 1110, 841, 813, 770, 508. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.91 (d, J=2.4 Hz, 1H), 8.58 (td, J=8.4, 2.4 Hz, 1H), 7.87 (d, J=8.2 Hz, 1H), 7.62 (d, J=8.2 Hz, 1H), 7.45 (d, J=8.9 Hz, 2H), 7.03 (dd, J=8.5 Hz, J=2.9 Hz, 1H), 6.81 (s, 1H), 6.67 (d, J=8.9 Hz, 2H), 3.01 (s, 6H), 1.74 (s, 9H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 163.8 (d, J=240.1 Hz, Cq), 150.5 (Cq), 149.0 (Cq), 148.3 (Cq), 148.1 (Cq), 146.1 (d, J=15.2 Hz, CH), 139.9 (d, J=8.1 Hz, CH), 133.7 (d, J=4.7 Hz, Cq), 132.9 (2CH), 129.0 (CH), 123.3 (Cq), 121.0 (Cq), 115.4 (CH), 111.8 (2CH), 111.0 (CH), 109.4 (d, J=37.4 Hz, CH), 98.3 (Cq), 84.4 (2Cq), 79.7 (Cq), 40.1 (2CH.sub.3), 28.3 (3CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) 72.03. HRMS (+ESI) calculated for C.sub.27H.sub.25FN.sub.4O.sub.2 (M+H+): 457.2034, found: 457.2036.

Example 12.6 4-((6-(6-Fluoropyridin-3-yl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 25c

(163) ##STR00232##

(164) The compound was prepared according to procedure F and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). Yellow solid (68%), mp 251-253 C., Rf=0.19 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3140, 2899, 2197, 1610, 1540, 1470, 1415, 1371, 1291, 1273, 1187, 1140, 1065, 1019, 948, 814, 761, 699, 645, 567, 520. .sup.1H NMR (250 MHz, 20 C.) 12.24 (s, 1H), 8.94 (d, J=2.4 Hz, 1H), 8.65 (td, J=8.4 Hz, J=2.7 Hz, 1H), 8.06 (d, J=8.3 Hz, 1H), 7.77 (d, J=8.3 Hz, 1H), 7.41 (d, J=8.9 Hz, 2H), 7.31 (dd, J=8.7 Hz, J=2.7 Hz, 1H), 6.83-6.68 (m, 3H), 2.98 (s, 6H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 159.8 (d, J=222.0 Hz, Cq), 150.9 (Cq), 148.8 (Cq), 147.6 (Cq), 146.0 (d, J=15.7 Hz, CH), 140.4 (d, J=8.0 Hz, CH), 134.2 (d, J=4.5 Hz, Cq), 132.9 (2CH), 129.5 (CH), 121.7 (Cq), 120.0 (Cq), 113.9 (CH), 112.4 (2CH), 110.0 (d, J=37.7 Hz, CH), 107.9 (Cq), 105.6 (CH), 95.5 (Cq), 80.5 (Cq), 40.1 (2CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 70.25. HRMS (+ESI) calculated for C.sub.22H.sub.18FN.sub.4 (M+H+): 357.1510, found: 357.1507.

Example 13. Synthesis of the Final Fluorinated Alkyl Compounds

(165) The derivatives of 7-azaindole, having a fluoroethyl group on the amine of the N-methylaniline were obtained by two different methods.

(166) Method 1

(167) The first method consists of performing a nucleophilic substitution reaction of the secondary amine intermediate 23i. The product 26 was obtained in a yield of 31%. Alcohol 26 was then converted to fluoro derivative 27 in the presence of DAST in a yield of 27%. This compound was deprotected with a solution of TFA in CH.sub.2Cl.sub.2 to give the final product 28 with a yield of 26%.

(168) ##STR00233##

(169) To prepare compounds radiolabeled with .sup.18F, O-tosyl derivative 29 was prepared from 26

(170) ##STR00234##

Example 13.1 tert-Butyl-2-((4-((2-hydroxyethyl)(methyl)amino)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 26

(171) ##STR00235##

(172) To a solution containing derivative 23i (0.6 g, 1.73 mmol, 1 eq.), 2-bromoethanol (0.55 ml, 7.77 mmol, 4.5 eq.) and KI (0.06 g, 0.35 mmol, 0.2 eq.) in acetonitrile (30 ml) was added a solution of t-BuOK (1M in THF, 3.8 ml, 3.80 mmol, 2.2 eq.). The mixture was stirred at reflux for 8 days (TLC monitoring) with adding 4 eq. 2-bromoethanol every 24 hours. At the end of the reaction water was added to the reaction mixture, the phases were separated, and the aqueous phase was extracted with ethyl acetate. The combined organic phases were washed with water, a saturated NaCl solution and dried over MgSO.sub.4 before being concentrated under reduced pressure. The compound was purified by flash column chromatographie on silicagel (ethyl acetate/petroleum ether=50/50+1% MeOH). yellow solid (31%), mp 154-156 C., Rf=0.22 (ethyl acetate/petroleum ether=40/60). IR (v, cm.sup.1, neat) 3386, 2980, 2926, 2206, 1747, 1603, 1546, 1517, 1473, 1408, 1384, 1343, 1305, 1249, 1194, 1154, 1117, 1085, 980, 847, 831, 814, 776, 746, 643, 525. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.50 (dd, J=4.8 Hz, J=1.7 Hz, 1H), 7.81 (dd, J=7.8 Hz, J=1.7 Hz, 1H), 7.46-7.34 (m, 2H), 7.17 (dd, J=7.8 Hz, J=4.8 Hz, 1H), 6.80 (s, 1H), 6.79-6.64 (m, 2H), 3.85 (t, J=5.7 Hz, 2H), 3.54 (t, J=5.7 Hz, 2H), 3.04 (s, 3H), 1.82 (1s, 1H), 1.68 (s, 9H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 149.8 (Cq), 148.6 (CH), 148.1 (Cq), 145.7 (Cq), 132.8 (2CH), 128.3 (CH), 121.9 (Cq), 121.6 (Cq), 118.8 (CH), 112.1 (2CH), 111.7 (CH), 109.9 (Cq), 96.9 (Cq), 84.6 (Cq), 79.8 (Cq), 60.2 (CH.sub.2), 54.8 (CH.sub.2), 38.9 (CH.sub.3), 28.2 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.23H.sub.26N.sub.3O.sub.3 (M+H+): 392.1969, found: 392.1968.

Example 13.2 tert-Butyl-2-((4-(methyl(2-(tosyloxy)ethyl)amino)phenyl)ethynyl)-1H-pyrrol[2,3-b] pyridine-1-carboxylate 29

(173) ##STR00236##

(174) To a solution of TsCl (0.12 g, 0.63 mmol, 1.2 eq.), triethylamine (0.15 ml, 1.05 mmol, 2 eq.) and DMAP (0.013 g, 0.3 1 mmol, 0.2 eq.) in THF (11 ml), cooled to 0 C., was added a solution of 26 (0.21 g, 0.53 mmol, 1 eq.) in THF (6 ml). The mixture was stirred at room temperature overnight, concentrated under reduced pressure and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=30/70). Yellow solid (55%), mp 171-173 C., Rf=0.38 (ethyl acetate/petroleum ether=40/60). IR (v, cm.sup.1, neat) 2986, 2360, 2198, 1749, 1605, 1544, 1514, 1407, 1348, 1306, 1253, 1187, 1170, 1114, 1092, 1010, 972, 900, 804, 776, 663, 556, 508. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.48 (dd, J=4.8, 1.7 Hz, 1H), 7.78 (dd, J=7.8 Hz, J=1.7 Hz, 1H), 7.73-7.52 (m, 2H), 7.39-7.26 (m, 2H), 7.30-7.17 (m, 2H), 7.14 (dd, J=7.8 Hz, J=4.8 Hz, 1H), 6.78 (s, 1H), 6.56-6.42 (m, 2H), 4.16 (t, J=5.8 Hz, 2H), 3.62 (t, J=5.8 Hz, 2H), 2.90 (s, 3H), 2.39 (s, 3H), 1.66 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 148.6 (Cq), 148.3 (Cq), 148.1 (Cq), 145.8 (CH), 145.0 (Cq), 132.8 (2CH), 132.6 (Cq), 129.8 (2CH), 128.3 (CH), 127.8 (2CH), 121.9 (Cq), 121.5 (Cq), 118.9 (CH), 111.8 (CH), 111.6 (2CH), 110.0 (Cq), 96.7 (Cq), 84.6 (Cq), 79.9 (Cq), 66.7 (CH.sub.2), 51.0 (CH.sub.2), 39.0 (CH.sub.3), 28.2 (3CH.sub.3), 21.7 (CH.sub.3). HRMS (+ESI) calculated for C.sub.30H.sub.32N.sub.3O.sub.5S (M+H+): 546.2057, found: 546.2053.

Example 13.3 tert-Butyl-2-((4-((2-fluoroethyl)(methyl)amino)phenyl)ethynyl)-1H-pyrrolo[2,3-b] pyridine-1-carboxylate 27

(175) ##STR00237##

(176) To a solution containing compound 26 (0.1 5 g, 0.29 mmol, 1 eq.) in dichloromethane (3 ml) and cooled to 78 C. was added dropwise DAST (0.077 ml, 0.59 mmol, 2 eq.). The reaction mixture was stirred for 1 h at 78 C. After returning to room temperature, water and dichloromethane were added and the phases were separated. The aqueous phase was extracted with dichloromethane (2 times), the combined organic phases were dried over MgSO.sub.4 and concentrated under reduced pressure. The compound was purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80). White solid (22%), mp 151-153 C., Rf=0.31 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 2979, 2204, 1742, 1605, 1573, 1544, 1517, 1355, 1306, 1253, 1189, 1154, 1115, 1089, 1041, 979, 813, 774, 527, 510, 508, 504. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.48 (dt, J=4.8 Hz, J=1.6 Hz, 1H), 7.78 (dt, J=7.9 Hz, J=1.6 Hz, 1H), 7.44-7.34 (m, 2H), 7.15 (ddd, J=7.8 Hz, J=4.8 Hz, J=1.4 Hz, 1H), 6.78 (s, 1H), 6.66 (d, J=8.8 Hz, 2H), 4.69 (t, J=5.1 Hz, 1H), 4.50 (t, J=5.1 Hz, 1H), 3.72 (t, J=5.2 Hz, 1H), 3.62 (t, J=5.2 Hz, 1H), 3.04 (m, 3H), 1.66 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 149.1 (Cq), 148.7 (Cq), 148.2 (Cq), 145.9 (CH), 133.0 (2CH), 128.5 (CH), 122.1 (Cq), 121.7 (Cq), 119.0 (CH), 111.9 (2CH), 111.8 (CH), 109.9 (Cq), 96.9 (Cq), 84.7 (Cq), 81.8 (d, J=170.3 Hz, CH.sub.2), 80.0 (Cq), 52.5 (d, J=21.2 Hz, CH.sub.2), 39.1 (CH.sub.3), 28.3 (3CH.sub.3). 1.sup.9F NMR (235 MHz, CDCl.sub.3, 20 C.) 222.2. HRMS (+ESI) calculated for C.sub.23H.sub.25FN.sub.3O.sub.2 (M+H+): 394.1925, found: 394.1925.

Example 13.4 4-((1H-Pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 28

(177) ##STR00238##

(178) The compound was prepared according to procedure F (26%), or according to procedure C (83% see Method 2, described below) and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). Yellow solid (83%), mp 242-244 C., Rf=0.28 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3113, 3057, 2977, 2892, 2808, 2360, 2202, 1601, 1536, 1510, 1432, 1405, 1378, 1353, 1324, 1278, 1236, 1214, 1187, 1137, 1076, 1042, 1012, 977, 916, 810, 766, 692, 624, 552, 515. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.07 (s, 1H), 8.24 (m, 1H), 7.90 (m, 1H), 7.39 (d, J=8.4 Hz, 2H), 7.08 (dd, J=7.9 Hz, J=4.6 Hz, 1H), 6.78 (d, J=8.4 Hz, 2H), 6.71 (d, J=1.7 Hz, 1H), 4.66 (t, J=5.0 Hz, 1H), 4.54 (t, J=5.0 Hz, 1H), 3.76 (t, J=5.1 Hz, 1H), 3.69 (t, J=5.1 Hz, 1H), 3.00 (s, 3H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 149.7 (Cq), 148.8 (Cq), 144.3 (CH), 133.0 (2CH), 128.4 (CH), 120.5 (Cq), 120.2 (Cq), 116.6 (CH), 112.4 (2CH), 108.3 (Cq), 105.5 (CH), 94.7 (Cq), 82.4 (d, J=166.2 Hz, CH.sub.2), 80.5 (Cq), 51.9 (d, J=19.8 Hz, CH.sub.2), 38.9 (CH.sub.3). .sup.19F NMR (235 MHz, DMSO-d.sub.6) 221.2 (tt, J=47.5 Hz, J=26.2 Hz). HRMS (+ESI) calculated for C.sub.18H.sub.17FN.sub.3 (M+H+): 294.1401, found: 294.1401.

Example 14. Synthesis of Final Fluorinated Alkyl Compounds

(179) Method 2:

(180) Compound 30, obtained by reductive amination of ethynylaniline, was engaged in an alkylation reaction with ethyl bromoacetate to give the derivative 31, which is then reduced with LiAIH.sub.4 to provide amino alcohol 32. The latter was transformed to tosylate 33 and subsequently substituted with fluorine in the presence of TBAF to give alkyne 34, which is used for the Sonogashira coupling to give the desired product 28 or its analogue 35

(181) ##STR00239##

(182) Thereafter, the alkynes 31 and 36 (methylated analogues of 32) were used to exemplify the group of 5-fluoro-1H-pyrrolo[2,3-b]pyridine. Thus, the products 37 and 38, obtained from the Sonogashira coupling with the derivative 18 g were obtained with yields of 93% and 80% respectively

(183) ##STR00240##

Example 14.1 Ethyl 2-((4-ethynylphenyl)(methyl)amino)acetate 31

(184) ##STR00241##

(185) 4-ethynyl-N-methylaniline (2.05 g, 15.6 mmol, 1 eq.) and Na.sub.2CO.sub.3 (2.49 g, 23.4 mmol, 1.5 eq.) were dissolved in EtOH (30 ml), and ethyl bromoacetate (1.83 ml, 17.19 mmol, 1.1 eq.) was slowly added. the reaction medium was at reflux for 1 day. After cooling, water (70 ml) and ethyl acetate (40 ml) were added and the compound was extracted with ethyl acetate (3 times). The organic phase was dried over MgSO.sub.4 and concentrated under reduced pressure before being purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=5/95). transparent liquid (3.18 g, 94%), Rf=0.34 (ethyl acetate/petroleum ether=5/95). IR (v, cm.sup.1, neat) 3282, 2981, 2099, 1741, 1607, 1515, 1476, 1370, 1250, 1181, 1115, 1026, 946, 816, 662, 538, 505. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.42-7.34 (m, 2H), 6.65-6.56 (m, 2H), 4.20 (q, J=7.1 Hz, 2H), 4.08 (s, 2H), 3.09 (s, 3H), 2.99 (s, 1H), 1.26 (t, J=7.1 Hz, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 170.5 (Cq), 149.0 (Cq), 133.3 (2CH), 111.8 (2CH), 110.0 (Cq), 84.6 (Cq), 75.0 (CH), 61.1 (CH.sub.2), 54.2 (CH.sub.2), 39.5 (CH.sub.3), 14.2 (CH.sub.3). HRMS (+ESI) calculated for C.sub.13H.sub.16NO.sub.2 (M+H+): 218.1176, found: 218.1175.

Example 14.2 2-((4-Ethynylphenyl)(methyl)amino)ethanol 32

(186) ##STR00242##

(187) To a solution of 31 (0.518 g, 2.38 mmol, 1 eq.) in THF (2.4 ml) was slowly added a 1M solution of LiAlH.sub.4 in THF (4.8 ml, 4.76 mmol, 2 eq.). The mixture was stirred at room temperature for 1 hour and then for 4 hours at reflux. After cooling to 0 C., were added water, a saturated aqueous solution of NaCl and Et.sub.2O. The suspension was filtered over celite and washed with Et.sub.2O. The filtrate was separated into two phases and the aqueous phase was washed 3 times with Et.sub.2O. The combined organic layers were dried over MgSO.sub.4 and concentrated in reduced pressure. The crude product was purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80). White solid (0.36 g, 85%), mp 73-75 C., Rf=0.36 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3293, 3271, 2907, 2871, 2094, 1606, 1518, 1454, 1378, 1349, 1268, 1222, 1176, 1125, 1059, 977, 908, 852, 814, 803, 644, 581, 524, 509. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.37-7.28 (m, 2H), 6.70-6.60 (m, 2H), 3.79 (q, J=5.6 Hz, 2H), 3.48 (t, J=5.6 Hz, 2H), 2.97 (s, 3H), 2.95 (s, 1H), 1.62 (1s, 1H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 149.8 (Cq), 133.3 (2CH), 112.0 (2CH), 109.4 (Cq), 84.6 (Cq), 75.0 (CH), 60.2 (CH.sub.2), 54.8 (CH.sub.2), 38.8 (CH.sub.3). HRMS (+ESI) calculated for C.sub.11H.sub.14NO (M+H+): 176.1070, found: 176.1071.

Example 14.3 2-((4-Ethynylphenyl)(methyl)amino)ethyl 4-methylbenzenesulfonate 33

(188) ##STR00243##

(189) To a solution of TsCl (0.30 g, 1.55 mmol, 1.2 eq.), triethylamine (0.36 ml, 2.58 mmol, 2 eq.) and DMAP (0.032 g, 0.26 mmol, 0.2 eq.) in THF (27 ml), cooled to 0 C., was added a solution of 32 (0.23 g, 1.29 mmol, 1 eq.) in THF (15 ml). The mixture was stirred at room temperature overnight, concentrated under reduced pressure and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). White solid (85%), mp 99-101 C., Rf=0.38 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3278, 2991, 2920, 2099, 1608, 1519, 1351, 1293, 1268, 1240, 1217, 1172, 1145, 1093, 1078, 1015, 959, 918, 898, 842, 817, 777, 692, 658, 578, 556, 523. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.75-7.53 (m, 2H), 7.36-7.07 (m, 4H), 6.55-6.18 (m, 2H), 4.14 (t, J=5.8 Hz, 2H), 3.59 (t, J=5.8 Hz, 2H), 2.95 (s, 1H), 2.87 (s, 3H), 2.39 (s, 3H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 148.2 (Cq), 145.0 (Cq), 133.3 (2CH), 132.5 (Cq), 129.8 (2CH), 127.8 (2CH), 111.5 (2CH), 109.5 (Cq), 84.5 (Cq), 75.1 (Cq), 66.7 (CH.sub.2), 50.9 (CH.sub.2), 39.0 (CH.sub.3), 21.6 (CH.sub.3). HRMS (+ESI) calculated for C.sub.18H.sub.20NO.sub.3S (M+H+): 330.1158, found: 330.1158.

Example 14.4 4-Ethynyl-N-(2-fluoroethyl)-N-methylaniline 34

(190) ##STR00244##

(191) To a solution of 33 (0.21 g, 0.65 mmol, 1 eq.) In CH.sub.3CN (5 ml) was added a solution of TBAF 1M in THF (1.30 ml, 1.29 mmol, 2 eq.). The mixture was stirred at room temperature overnight, and 4 hours at 40 C. before being concentrated under reduced pressure and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=5/95). transparent liquid (68%), Rf=0.39 (ethyl acetate/petroleum ether=5/95). IR (v, cm.sup.1, neat) 3291, 2896, 2098, 1606, 1515, 1479, 1373, 1267, 1209, 1179, 1133, 1075, 1040, 1006, 979, 907, 846, 816, 845, 537, 520. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.39-7.27 (m, 2H), 6.67-6.45 (m, 2H), 4.66 (t, J=5.2 Hz, 1H), 4.47 (t, J=5.2 Hz, 1H), 3.68 (t, J=5.2 Hz, 1H), 3.58 (t, J=5.2 Hz, 1H), 3.00 (s, 3H), 2.96 (s, 1H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 148.9 (Cq), 133.4 (2CH), 111.6 (2CH), 109.3 (Cq), 84.6 (CH), 81.6 (d, J=170.1 Hz, CH.sub.2), 75.0 (CH), 52.4 (d, J=21.2 Hz, CH.sub.2), 39.0 (CH.sub.3). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) 50.0. HRMS (+ESI) calculated for C.sub.11H.sub.13FN (M+H+): 178.1027, found: 178.1026.

Example 14.5 4-((1H-Pyrrolo[3,2-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 35

(192) ##STR00245##

(193) The compound was prepared according to Procedure C and purified by column chromatography on silicagel under pressure (ethyl acetate/petroleum ether=20/80). Yellow solid (94%), mp 232-234 C., Rf=0.24 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3066, 2952, 2890, 2820, 2703, 2202, 1606, 1571, 1538, 1513, 1405, 1376, 1354, 1285, 1247, 1189, 1124, 1040, 982, 913, 815, 776, 623, 583, 557, 529, 515, 506. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 11.83 (s, 1H), 8.35 (d, J=4.6 Hz, 1H), 7.69 (m, 1H), 7.50-7.31 (m, 2H), 7.14 (dd, J=8.2 Hz, J=4.6 Hz, 1H), 6.89-6.69 (m, 3H), 4.67 (t, J=4.9 Hz, 1H), 4.55 (t, J=4.9 Hz, 1H), 3.76 (t, J=5.0 Hz, 1H), 3.70 (t, J=5.0 Hz, 1H), 3.00 (s, 3H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 149.7 (Cq), 145.9 (Cq), 143.8 (CH), 133.0 (2CH), 129.7 (Cq), 123.1 (Cq), 118.4 (CH), 117.8 (CH), 112.4 (2CH), 108.1 (Cq), 106.8 (CH), 95.2 (Cq), 82.4 (d, J=166.2 Hz, CH.sub.2), 80.4 (Cq), 51.9 (d, J=19.8 Hz, CH.sub.2), 38.8 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 15.8. HRMS (+ESI) calculated for C.sub.18H.sub.17FN.sub.3 (M+H+): 294.1401, found: 294.1404.

Example 14.6 4-Ethynyl-N-(2-methoxyethyl)-N-methylaniline 36

(194) ##STR00246##

(195) To a solution of 32 (0.25 g, 1.43 mmole, 1 eq.) in THF (3 ml) was slowly added a 1M solution of tBuOK in THF (2.85 ml, 2.85 mmol, 2 eq.). The mixture was stirred under ultrasound conditions for 5 minutes, cooled to 0 C. and methyl iodide was added dropwise. The reaction medium was stirred at room temperature for 16 h and concentrated in vacuo. The residue was taken up in ethyl acetate and the insoluble precipitate was filtered. To the filtrate was added water and the phases were separated. The aqueous phase was extracted with ethyl acetate (2 times). The combined organic phases were washed with a saturated NaCl solution, dried over MgSO.sub.4 and concentrated under reduced pressure. The product was purified by pressurized silicagel column chromatography (the ratio of solvents used: ethyl acetate/petroleum ether=5/95). Transparent liquid (0.22 g, 81%), Rf=0.21 (ethyl acetate/petroleum ether=2/98). IR (v, cm.sup.1, neat) 3286, 2877, 2097, 1606, 1515, 1451, 1375, 1274, 1193, 1179, 1110, 1067, 1018, 815, 644, 530, 514, 506, 503. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 6 7.38 (d, J=9.0 Hz, 2H), 6.65 (d, J=9.0 Hz, 2H), 3.56 (t, J=3.1 Hz, 4H), 3.37 (s, 3H), 3.02 (s, 3H), 3.00 (s, 1H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 149.3 (Cq), 133.3 (2CH), 111.5 (2CH), 108.7 (Cq), 84.8 (Cq), 74.8 (CH), 70.1 (CH.sub.2), 59.1 (CH.sub.3), 52.1 (CH.sub.2), 38.9 (CH.sub.3). HRMS (+ESI) calculated for C.sub.12H.sub.16NO (M+H.sup.+): 190.1226, found: 190.1225.

Example 14.7 2-((4-((5-Fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl) (methyl)amino)acetate d'ethyle 37

(196) ##STR00247##

(197) The compound was prepared according to Procedure C and purified by column chromatography on silicagel under pressure (ethyl acetate/petroleum ether=15/85). White solid (93%), mp 186-188 C., Rf=0.24 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 2984, 2208, 1729, 1608, 1585, 1540, 1508, 1372, 1295, 1254, 1190, 1154, 1109, 1030, 948, 871, 805, 765, 526, 514, 506, 503. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 10.59 (s, 1H), 8.25 (t, J=2.3 Hz, 1H), 7.60 (dd, J=8.9 Hz, J=2.6 Hz, 1H), 7.52-7.42 (m, 2H), 6.80-6.49 (m, 3H), 4.23 (q, J=7.1 Hz, 2H), 4.12 (s, 2H), 3.14 (s, 3H), 1.28 (t, J=7.1 Hz, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 170.4 (Cq), 155.9 (d, J=241.9 Hz), 149.3 (Cq), 145.0 (Cq), 133.0 (2CH), 131.9 (d, J=29.8 Hz, CH), 122.0 (Cq), 120.9 (d, J=7.3 Hz, Cq), 114.0 (d, J=21.0 Hz, CH), 112.0 (2CH), 109.8 (Cq), 105.4 (d, J=4.4 Hz, CH), 95.3 (Cq), 79.3 (Cq), 61.2 (CH.sub.2), 54.2 (CH.sub.2), 39.5 (CH.sub.3), 14.2 (CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) 138.3.

(198) HRMS (+ESI) calculated for C.sub.20H.sub.19FN.sub.3O.sub.2 (M+H+): 352.1456, found: 352.1457.

Example 14.8 4-((5-Fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-methoxyethyl)-N-methylaniline 38

(199) ##STR00248##

(200) The compound was prepared according to Procedure C and purified by column chromatography on silicagel under pressure (ethyl acetate/petroleum ether=20/80). White solid (80%), mp 160-162 C., Rf=0.35 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3066, 2882, 2203, 1602, 1534, 1507, 1372, 1346, 1293, 1218, 1189, 1155, 1106, 1019, 984, 895, 876, 821, 760, 553, 514, 506, 502. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 10.46 (s, 1H), 8.22 (t, J=2.3 Hz, 1H), 7.57 (dd, J=8.9 Hz, J=2.6 Hz, 1H), 7.47-7.41 (m, 2H), 6.74-6.67 (m, 2H), 6.65 (d, J=2.0 Hz, 1H), 3.58 (s, 4H), 3.37 (s, 3H), 3.04 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 155.9 (d, J=241.7 Hz, Cq), 149.5 (Cq), 145.1 (Cq), 133.0 (2CH), 131.9 (d, J=29.7 Hz, CH), 123.1 (Cq), 120.9 (d, J=7.2 Hz, Cq), 113.9 (d, J=20.9 Hz, CH), 111.7 (2CH), 108.4 (Cq), 105.2 (d, J=4.4 Hz, CH), 95.7 (Cq), 79.1 (Cq), 70.1 (CH.sub.2), 59.1 (CH.sub.3), 52.1 (CH.sub.2), 38.9 (CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) 138.4. HRMS (+ESI) calculated for C.sub.19H.sub.19FN.sub.3O (M+H+): 324.1507, found: 324.1507.

Example 15. Production of Fluorinated Ligands Labeled .SUP.18.F by Nucleophilic Substitution

(201) Step: Production of Fluoride Ions and Assessment of their Reactivity

(202) [.sup.18F] ions were produced by nuclear transmutation .sup.18O(p,n).sup.18F. The ion solution [.sup.18F] was passed over an QMA anion exchange cartridge for fixing the fluoride ions. This cartridge was pre-conditioned with 10 ml of K.sub.2CO.sub.3 and then rinsed with 10 ml of water. [.sup.18F] ions were eluted from the QMA cartridge with an aqueous solution of K.sub.2CO.sub.3 and Kyptofix.sub.2.2.2 dissolved in MeCN. This solution was transferred into a reactor and dried twice by azeotropic distillation with the addition of 1 ml MeCN each time. At the end of the drying, the complex with fluoride ions was ready for the next step of radiofluorination.

(203) Step: Nucleophilic Substitution (Aliphatic, Aromatic, Heteroaromatic)

(204) The syntheses are carried from (hetero)aromatic aryliodonium compounds, of electronically impoverished (heteroaryl)nitro, of (hetero)aryltrimethylammonium, of (hetero)aromatic boronic esters or acids, but also halogenated aliphatic compounds (Cl, Br, I), triflates or mesylates. The precursor, dissolved in a solvent (MeCN, DMSO, DMF or the like), was added to the reactor containing the complex with fluoride ions. For aliphatic substitutions MeCN was mainly used but, if necessary, solvents with higher boiling points can be used for the (hetero)aromatics substitutions, which typically require solvents such as DMSO or DMF. The reaction medium was thermally heated to between 5 and 30 min or by microwave, and then the solution was cooled to room temperature. This was diluted with water and possibly hydrolyzed, depending on the nature of the precursor used (removal of a protecting group). The approach described above is direct. An indirect approach depending on the accessibility of the molecule, the precursor may be considered. For example, the [.sup.18F] fluoroethyltosylate ([.sup.18F] FETos) was prepared from ethylene ditosylate, followed by an N, O or S alkylation of the precursor to give the desired product.

(205) Step: Purification and Formulation

(206) The crude reaction mixture was passed through a pre-purification cartridge and rinsed with water. The radiotracer was eluted from the cartridge with MeCN and the solution was loaded onto a semi-preparative column. The radiolabelled product of interest was collected and dissolved in water and trapped on a cartridge. It was rinsed and the radiopharmaceutical was eluted with injectable ethanol. The formulation was completed by addition of NaCl 0.9% so that no more than 10% ethanol, by weight, was present in the radiopharmaceutical medicine solution. The solution was passed through a sterilizing filter and dispensed into sterile and pyrogenic vials before being dispensed.

Example 16. Production of Carbon-11 Radiolabeled Ligands

(207) Step: production of reactive synthons labeled with Carbon-11

(208) [.sup.11C] ions were produced by nuclear transmutation .sup.11C(p,).sup.15N. This transmutation occurs in the presence of a few ppm of hydrogen or oxygen to lead to the formation of carbon-11 radiolabeled methane or carbon dioxide respectively. These two building blocks will pave the way for the production of many other building blocks radiolabeled with carbon-11 which will serve as reaction intermediates for incorporation in the molecule of interest. Among the most common compounds, methyl iodide or methyl triflate can be cited.

(209) FIG. 1a depicts the preparation of synthons from carbon dioxide radiolabeled with carbon-11 while

(210) FIG. 1b shows the preparation of synthons from methane radiolabeled with carbon-11.

(211) Step: Incorporating the Building Block to the Molecule of Interest.

(212) methyl iodide or methyl triflate radiolabeled with carbon-11 can be used in common reactions of O, N and S alkylation. The solvents used are: MeCN, DMSO, DMF or NMP. Coupling reactions with organometallic reagents can be used for these radiolabeled synthons: Stille, Suzuki, Sonogashira. Moreover, [.sup.11C]CO.sub.2 may be subject to attack from a Grignard reagent or be transformed into Grignard reagent. It can also be reduced by carbon monoxide, [.sup.11C]CO, and provide access to many chemical functions. FIG. 2 shows the chemical functionalities accessible via carbonylation reactions. The Carbon-11 labeling reactions are therefore mostly multistep reactions.

(213) Step: Purification and Formulation

(214) The crude reaction mixture was passed through a pre-purification cartridge then rinsed with water. The radiotracer was eluted from the cartridge with MeCN and the solution was loaded onto a semi-preparative column. The radiolabelled product of interest was collected and then dissolved in water and trapped on a cartridge. It was rinsed and the radiopharmaceutical was eluted with injectable ethanol and the formulation was completed by addition of NaCl 0.9% so that no more than 10% ethanol, by weight, was present in the radiopharmaceutical medicine solution. The solution was passed through a sterilizing filter and dispensed into sterile and pyrogenic vials before being dispensed.

Example 17. Production of Ligands Radiolabeled with Iodine-123

(215) The commercial solution of Na.sup.123I was acidified with ethanolic hydrogen chloride or sulfuric acid and then were added: ethanolic aromatic or heteroaromatic stannyl precursor (SnBu.sub.3 or SnMe.sub.3) a solution of oxidizing agent (Chloramine T, hydrogen peroxide or iodo-bead)

(216) The mixture was then stirred at room temperature for a few minutes (2-30 min). The solution was basified by addition of a solution NH.sub.4OH or NaHCO.sub.3. The reaction medium was purified by HPLC, the radiolabelled product of interest was collected and dissolved in water and trapped on a cartridge. It was rinsed and the radiopharmaceutical was eluted with injectable ethanol and the formulation was completed by addition of NaCl 0.9% so that no more than 10% ethanol, by weight, was present in the radiopharmaceutical medicine solution. The solution was passed through a sterilizing filter and dispensed into sterile and pyrogenic vials before being dispensed.

(217) A similar approach can be applied for compounds radiolabeled with other isotopes of iodine (124, 125, 131).

Example 18. Radiosynthesis

Example 18.1

(218) ##STR00249##

(219) The radiosynthesis of 28 was carried out using a FXFNpro (GE Healthcare) equipment. [.sup.18F] ions were produced by .sup.18O(p,n).sup.18F nuclear transmutation using a cyclotron PETtrace (GE Healthcare). The activity produced was transferred to the radiosynthesis automate and trapped on a QMA anion exchange cartridge (Waters) for fixing the fluoride ions. This cartridge was previously conditioned with 10 ml of K.sub.2CO.sub.3 and rinsed with 10 ml of water. [.sup.18F] ions were eluted from the QMA cartridge with an aqueous solution of K.sub.2CO.sub.3 and Kyptofix.sub.2,2,2 dissolved in MeCN (7.2 g of K.sub.2.2.2 2+715 l MeCN and 3.8 mg of K.sub.2CO.sub.3+285 l H.sub.2O). This solution was transferred into a reactor and dried twice by azeotropic distillation with the addition each time of 1 ml MeCN. At the end of drying the complex with the fluoride ions was ready for the next step of radiofluorination. 2 mg of precursor 29 having the tosyl function, dissolved in 700 of MeCN are added to the fluoride ions. The reaction mixture was maintained at 90 C. for 10 min. The solution was then brought to room temperature before adding 500 l of 1M HCl. The reaction was stirred 5 min at room temperature before being quenched by the addition of 8 ml of water. The mixture was then pre-purified on a preconditioned tC 18plus cartridge (Waters). The cartridge was washed with 5 ml of water prior to eluting the crude product of interest with 2 ml of MeCN to which were added 2 ml of 0.1 M ammonium acetate.

(220) The collected 4 ml were then loaded into a HPLC loop and injected onto a semi-preparative column Zorbax Eclipse XDB-C18 9,4250 mm 5 g (Agilent) with a MeCN/0.1M ammonium acetate 50:50 mobile phase at a rate of 5 ml/min. Under these conditions, the product of interest, [.sup.18F]28, was collected with a retention time of about 23 min. The collected product was dissolved in 25 ml of water and then trapped on a previously conditioned tC18light cartridge (Waters). The cartridge was rinsed with 5 ml of water. [.sup.18F]28 was eluted from the cartridge with 1 ml of injectable ethanol. The formulation was completed by the addition of 9 ml of 0.9% NaCl.

(221) For future injection to man the mother solution thus obtained must be aseptic according to GMP guidelines, with a double sterile filtration and filling the vials in a suitable environment under class A laminaRflow.

(222) [.sup.18F]28 was obtained in 855 min in a yield of 323% (corrected for decay). The specific activity determined from the calibration curve with the cold standard is of the order of 128 GBq/mole.

(223) FIG. 3 shows a quality control chromatogram of compound [.sup.18F]28.

Example 19. Biological Studies

(224) These are studies to determine the affinity and selectivity of the new compounds for -synuclein fibers. In order to identify better selectivity/affinity, the binding of molecules synthesized to the alpha-synuclein fibers is compared to their binding to the fibers of the -amyloid peptide (A1-42) and/or Tau. They are made by in vitro binding study on preparations of synthetic fibers of -synuclein (-syn), of (-amyloid peptide (A1-42) or Tau in two ways: 1/competition between the new compound and thioflavin T (ThT), and measuring fluorescence from the bound ThT, 2/direct binding of the new compound and measuring fluorescence from the bound fraction.

Example 19.1 Expression and Purification of -Syn, AI-42 and Tau Recombinant Proteins

(225) The -syn and A1-42 native proteins are expressed in E. coli (strain BL21 (DE3), (Stratagene, La Jolla, Calif.)) and purified according to described methods (Ghee M., Melki R., Michot N., Mallet J. PA700, the regulatory complex of the 26S proteasome, interferes with -synuclein assembly. FEBS J. 2005, 272:4023-4033; Walsh D M, Thulin E, Minogue A M, Gustavsson N, Pang E, Teplow D B, Linse S. A facile method for expression and purification of the Alzheimer's disease-associated amyloid beta-peptide. FEBS J. 2009, 276:1266-1281). The -syn concentration is determined by measuring the absorbance at 280 nm with a molar extinction coefficient of 5960 M.sup.1 cm.sup.1. For A1-42, the concentration is determined by fluorimetric method with the fluorescamine reagent (Sigma) which reacts with primary amines to form a fluorescent product (Udenfriend S, Stein S, Bhlen P, Dairman W, Leimgruber W, Weigele M. Fluorescamine: a reagent for assay of amino acids, peptides, proteins, and primary amines in the picomolar range. Science 1972, 178:871-872).

(226) Human Tau protein (isoform h2N4RTau) is expressed in the vector pET11d in E. Coli (strain BL21 (DE3), (Stratagene, La Jolla, Calif.)) and purified according to the described method (Barghorn S, Biernat J, Mandelkow E. (2005) Methods Mol Biol. 299:35-51). The Tau purified concentration is determined by measuring the absorbance at 280 nm using a molar extinction coefficient of 7450 M.sup.1 cm.sup.1.

Example 19.2 Production and Characterization of -Syn, A1-42 and Tau Fibers

(227) To obtain fiber assembly, -syn is incubated in Tris-HCl 50 mM pH7.5, KCl 150 mM at 37 C. under continuous agitation during 4 days. The lyophilized A1-42 was dissolved in 1,1,1,3,3,3-Hexafluoro-2-propanol (HFIP) at 0.2 mg/mL and incubated for 24 h at 37 C. to obtain the complete solubilization. The HFIP is evaporated under nitrogen stream to obtain a dry product. To start the fiber assembly, the dry peptide is resuspended in PBS pH7.4, 10% (v/v) DMSO and incubated at 37 C. for 3 days without agitation.

(228) The assembly process is followed by measuring the binding of Thioflavin T (ThT) to the fibres (LeVine, H 3rd. Thioflavine T interaction with synthetic Alzheimer's disease beta-amyloid peptides: detection of amyloid aggregation in solution. Protein Sci. 1993, 2: 404-410). At regular intervals, 10 L protein aliquots are collected and mixed with 400 L of ThT (10 M) in water. The fluorescence of ThT is measured using a Cary Eclipse Spectrofluorometer (Varian Inc., Palo Alto, USA) (excitation: 440 nm, emission: 480 nm). Protein fibers are systematically observed by electron microscopy (Jeol 1400). The images are recorded with a CCD camera (Gatan Orius). Finally, the percentage of -syn and A1-42 aggregated into fibers is checked on the pellet after centrifugation at 40000g for 20 min and determination of the concentration of soluble protein/peptide remaining in the supernatant.

(229) Tau protein in PBS buffer containing 1 mM DTT is assembled into fiber in the presence of one twelfth of a molar equivalent of heparin at 37 C. under stirring.

Example 19.3 In Vitro Inhibition of ThT Binding and Determination of K.SUB.i

(230) Fresh solutions of the test compounds (2.5 mM in DMSO) are diluted in PBS pH7.4, at concentrations between 0.5 nM and 5 M in the presence of -syn (200 nM), A1-42 (500 nM) or Tau (200 nM) fibres and ThT 500 nM in a final 2 mL volume. The samples are incubated for 1 h at room temperature (RT) to reach equilibrium. The binding of ThT to -syn, A1-42 or Tau fibres is measured by fluorescence (excitation: 440 nm, emission: 480 nm). Inhibition of ThT binding by increasing concentrations of each test compound is measured by fluorescence reduction. Due to the partial superposition between the emission spectra of some compounds and ThT, the compounds are also incubated with -syn, A1-42 or Tau fibers in the absence of ThT. For each concentration, the fluorescence values in the absence of ThT are subtracted from those in the presence of ThT. The results are expressed as a percentage of the maximum fluorescence value of the ThT measured in the absence of a competitor (100% bind). From each curve, the IC.sub.50 value is measured using the following equation:
Y=min+(maxmin)/1+(Y/IC.sub.50).sup.slope

(231) The Ki was then determined using the method of Cheng and Prusoff (Cheng Y, Prusoff W H. Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 percent inhibition (I50) of an enzymatic reaction. Biochem Pharmacol 1973, 22:3099-3108).
Ki=IC.sub.50/(1+[ThT]/Kd.sub.ThT)

(232) The equation takes into account the concentration of ThT used (500 nM) and its affinity (Kd.sub.ThT) for for -syn, A1-42 and/or Tau fibers, namely 700 nM, 500 nM, and 350 nM, respectively.

(233) The results obtained are summarized in Table 5.

(234) TABLE-US-00005 TABLE 5 Ki vs Thioflavin T measurement Ki A Ki syn Ki Tau Reference Structure (nM) (nM) (nM) AV45 2.2 1 76.6 44 30.6 9 FDDNP 4.6 3 25.1 5 9.5 1 22a 0 embedded image 24.5 9 4.7 2 4.61 0.2 22b 91.5 11 28.7 8 8.4 2 22c 21.3 7 26.0 16 12.0 1 22d 22e 909 143 49.9 12 25.1 8 22f 349 256 14.8 7 22g 318.2 95 19.0 8 22h 244.1 84 20.7 9 22i 22j 22k 0 22L 22m 22n 25a 25b 25c 28 35 37 38 0

Example 19.4 In Vitro Direct Determination of Kd and Bmax by Fluorescence

(235) For some of the compounds, the IC.sub.50 could not be determined because their emission spectra were confused with that of ThT. For these compounds as well as those (azaindole series) that showed significant competition with ThT, direct fluorescence measurements were performed to determine their affinity (Kd) and the density of binding sites (Bmax) to the fibers.

(236) Fresh solutions of each test compound (2.5 mM in DMSO) are diluted in PBS pH=7.4 at concentrations between 0.5 nM and 5 M in the presence or absence of -syn (200 nM), A1-42 (500 nM) or Tau (200 nM) fibers in a final 2 mL volume. After 1 h of incubation at RT, the binding of each compound to -syn, A131-42 or Tau fibers is measured by fluorescence using the spectral changes of the compounds during their binding to the fibers, using the appropriate excitation/emission wavelengths (those giving the highest fluorescence variation during binding to the fibres). For each concentration of compound added to the fibres, the bound and free fractions are measured by fluorescence according to the following equation:
F.sub.m=F.sub.BB+F.sub.F(TB)

(237) Where F.sub.m is the fluorescence measured in the presence of fibers at a concentration T of the compound added to the fibers, F.sub.B is the specific fluorescence of the bound compound, F.sub.F is the specific fluorescence of the free compound, and B is the concentration of the fiber bound compound at a given concentration T (Bell, J. E., Fluorescence; Solution Studies, Spectrometry in Biochemistry, vol. I, Bell, J. E., ed., CRC Press, Inc., Boca Raton, Fla., pp. 155-194 (1981)).

(238) The value of F.sub.F is determined by measuring the fluorescence of known concentrations of compounds in the absence of fibres. The F.sub.B value is determined by measuring the maximum fluorescence of known concentrations of compounds in the presence of saturated concentrations of -syn, A1-42, or Tau fibers.

(239) Thus, at each point, the concentration of bound compound B is determined according to the following equation:
B=(F.sub.mF.sub.FT)/(F.sub.BF.sub.F)

(240) The values of B thus determined versus the concentrations of the free fractions (T-B) are analyzed according to the Michaelis-Menten equation. The affinity (Kd) and density of binding sites within the fibers of -syn, A1-42 or Tau (Bmax) are determined by Scatchard analysis, which also makes it possible to highlight multiple site classes.

(241) The results obtained are shown in Tables 6 and 7.

(242) TABLE-US-00006 TABLE 6 -syn vs A Kd & Bmax measurement A Bmax1 syn Bmax1 nmol/mol prot nmol/mol prot A Kd1 (number of syn Kd1 (number of Reference Structure nM sites/monomer) nM sites/monomer) AV45 1.68 0.2 3.33 0.2 (1/300) 24.3 20 27.9 19 (1/35) FDDNP 4.2 1 10.2 1 (1/100) 16.1 6 39.5 10 (1/25) 22a embedded image 11.8 3 3.04 0.6 (1/300) 0.53 0.2 69.5 20 (1/14) 22b 5.2 3 2.3 0.8 (1/400) 1.4 1 80.0 42 (1/15) 22c 2.9 2 1.44 0.6 (1/700) 3.25 0.2 82.5 5 (1/12) 22d 3.6 2 2.4 0.8 (1/400) 1.0 0.5 6.0 1 (1/170) 22f 16.8 2 21.6 3 (1/50) 0.79 0.4 49.0 15 (1/20) 25a 4.9 0.6 5.8 0.32 (1/170) 0.49 0.2 53.5 10 (1/20) 25b embedded image 4.27 0.6 11.0 1 (1/90) 0.73 0.3 69.6 23 (1/14) 25c 3.1 1 11.0 2 (1/90) 1.27 0.4 130 30 (1/8) 28 1.2 1 1.8 0.6 (1/600) 2.4 1 141.5 45 (1/7)

(243) TABLE-US-00007 TABLE 7 -syn vs Tau Kd & Bmax measurement Tau Bmax1 syn Bmax1 nmol/mol prot nmol/mol prot Tau Kd1 (number of syn Kd1 (number of Reference Structure nM sites/monomer) nM sites/monomer) AV45 19.6 5 92.0 20 (1/11) 24.3 20 27.9 19 (1/35) FDDNP 34.9 6 138.5 16 (1/7) 16.1 6 39.5 10 (1/25) 22a 0 embedded image 0.44 0.1 93.0 15 (1/10) 0.53 0.2 69.5 20 (1/14) 22b 0.49 0.2 37.1 10 (1/30) 1.4 1 80.0 42 (1/15) 22c 0.13 0.05 26.5 5 (1/40) 3.25 0.2 82.5 5 (1/12) 22d 2.4 0.9 12.5 5 (1/80) 1.0 0.5 6.0 1 (1/170) 25a 1.67 0.5 70.4 4 (1/10) 0.49 0.2 53.5 10 (1/20) 28 0.97 0.4 46.5 5 (1/20) 2.4 1 141.5 45 (1/7)

Example 19.5 In Vivo Evaluation of a Fluorine-18-Labelled -Syn Tracer

(244) The objective is to determine whether the tracer binds in vivo to the -syn fibers after intravenous injection.

(245) Animal Model: Adult male rats of Wistar strain.

(246) Preparation of fiber: -syn fibers produced according to the protocol described in Example 19.2 were centrifuged at 16000g for 20 min to twice and resuspended in PBS pH 7.4.

(247) Preparation of the animals: the fibers are implanted by stereotactic surgery in the right striatum of anesthetized animal (Maia et al. Synapse 2012, 66:573-83).

(248) In vivo study: the fiber-bearing animal receives an intravenous injection of the tracer to be tested. From the moment of injection, imaging is carried out using a dedicated system (eXplore VISTA/CT) which records the intracerebral accumulation of radioactivity for 70 minutes. The analysis of the images obtained can quantify the binding of the tracer implanted in the striatum compared to the control side (Srrire et al. Nucl. Med. Biol. 2014, 41:103-13; Srrire et al. Neurobiol. Aging 2015, 36:1639-52).

Example 19.6 In Vivo Evaluation of a Fluorine-18-Labelled -Syn Tracer

(249) The objective is to determine whether the tracer has the blood-brain barrier (BBB) crossing properties in sufficient quantities to be used as a PET imaging tracer. In addition, bone fixation can be qualified, which reflects the degree of defluorination of the tracer in vivo.

(250) Animal Model: Adult male rats of Wistar strain.

(251) In vivo study: the healthy animal receives an intravenous injection of the tracer test (molecule 28).

(252) From the moment of injection, imaging is carried out using a dedicated system (PET/CT) which records the intracerebral accumulation of radioactivity (Srrire et al. Nucl. Med. Biol. 2014, 41:103-13; Srrire et al. Neurobiol. Aging 2015, 36:1639-52). At the end of the imaging, the animal is euthanized; the brain and a bone fragment (femur) are collected, weighed and their radioactivity is measured. This method allows to precisely quantify the accumulation of the tracer in the tissues. The results are expressed as a percentage of the injected tracer dose/g of tissue (% DI/g).

(253) Results:

(254) Passing of the BBB (0.4% DI/g)

(255) Weak binding to bone (0.3% DI/g)

Example 20. Procedure M (Buchwald Coupling)

(256) Under argon, Pd.sub.2dba.sub.3 (0.05 eq.) and BINAP (0.075 mmol) are added to an anhydrous toluene degassed solution of 0.3 M concentration containing the amine (1.0 eq.), 1,4-dibromobenzene (1.0 eq.) and tBuONa (1.2 eq.). After 16 h at 80 C., the solvent was evaporated under reduced pressure. Then, the reaction mixture was concentrated under reduced pressure, before being purified by flash column chromatography on silicagel.

Example 21. Procedure I (Preparation of True Alkynes)

Example II 21.1

(257) Under argon, Pd(PPh.sub.3).sub.2Cl.sub.2 (0.05 eq.) and CuI (0.1 mmol) are added to a degassed piperidine solution of 0.1 M concentration containing l'ethynyltrimethylsilane (4.0 eq.), the brominated derivative (1.0 eq.) and triphenylphosphine (0.2 eq.). After 16 h at 85 C., the solvent was evaporated under reduced pressure. Then, the reaction mixture was purified by flash column chromatography on silicagel. Then the alkyne intermediate is reacted with K.sub.2CO.sub.3 (1.5 eq.) in methanol (0.03 M). After 3 h at room temperature, the solvent was evaporated under reduced pressure. The crude is dissolved in 10 mL of ethyl acetate. Then the organic phase was washed with brine (310 mL). Then the organic phase is dried with MgSO.sub.4, filtered through cotton and evaporated under reduced pressure. Finally, the crude is purified by flash column chromatography on silicagel with eluting agent (ethyl acetate/petroleum ether) to afford the true alkyne.

Example 21.2. 12

(258) The catalyst [Pd(PPh.sub.3).sub.2Cl.sub.2] (0.025 eq.) was added to a degassed solution of the brominated 40 (1.0 eq.), Ethynyltrimethylsilane (1.4 eq.), CuI (0.05 eq.) in THF/Et.sub.3N (1/1). The mixture was stirred at room temperature for 20 h under argon. Then, the reaction mixture was concentrated under reduced pressure before being purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=2/98) to obtain the silylated intermediate which is reacted with KOH (2.0 eq.) in methanol. After 10 min stirring at room temperature, dichloromethane and water are added. The organic phases are extracted 3 times with dichloromethane. They are combined, dried over MgSO.sub.4, filtered through cotton and evaporated to dryness to yield the expected alkyne.

Example 22. Procedure J (Desylilation)

(259) At 0 C. under argon, a solution of TBAF in THF (C=1 M, 1.5 eq.) was added dropwise to the reaction mixture containing the silylated compound (1.0 eq.) diluted in THF. After 2 h at room temperature, water (20 ml) and ethyl acetate (20 ml) are successively added. The organic phases are extracted 3 times with ethyl acetate (20 ml), then they were combined, dried with MgSO filtered through cotton and evaporated under reduced pressure. Finally, the crude is purified by flash column chromatography on silica gel with eluting agent (methanol/dichloromethane) to yield the primary alcohol.

Example 23. Procedure (Reductive Amination)

(260) The aldehyde (1.0 eq.) is reacted with an amine (6.0 eq.) in the presence of NaBH(OAc).sub.3 (10 eq.) and Et.sub.3N (11 equiv.) in DCE. After 4 h at room temperature, the mixture was evaporated to dryness and then 10 ml of a saturated solution of NaHCO.sub.3 and 10 ml of ethyl acetate are added. The organic phase was extracted with ethyl acetate (310 ml). The organic phases are combined and washed with a saturated NaCl solution and then dried over MgSO.sub.4, filtered through cotton and evaporated to dryness. The crude was purified by flash chromatography column on silica gel to yield the expected compound.

Example 24. 2-{2-[4-(2-fluoroethoxy)phenyl]ethynyl}-1H-pyrrolo[2,3-b]pyridine 43

(261) 2-{2-[4-(2-fluoroethoxy)phenyl]ethynyl}-1H-pyrrolo[2,3-b]pyridine was synthesized in 3 steps. Initially, the corresponding alkyne was prepared in 2 steps and then we did the Sonogashira reaction with the azaindole to obtain the final compound.

Example 24.1 Preparation of 1-ethynyl-4-f2-fluoroethoxy) benzene 39

(262) The alkyne 39 was prepared in three steps by starting from 4-iodophenol 40. The first step has been described by Hirose et al. (Chemical Communications, 2009, 39 p 5832-.5834) and for the last two steps we used the method described by Ouach et al. (European Journal of Medicinal Chemistry, 2016, vol. 107, p. 153-164)

(263) ##STR00286##

(264) The catalyst [Pd(PPh.sub.3).sub.2Cl.sub.2] (39 mg, 0.055 mmol, 0.03 eq.) was added to a degassed solution of iodized 39 (400 mg, 1.82 mmol, 1.0 eq.), ethynyltrimethylsilane (0.386 ml, 2.73 mmol, 1.5 eq.), CuI (10.4 mg, 0.055 mmol, 0.03 eq.) in 6 ml of Et.sub.3 N. The mixture was stirred at 85 C. room for 4 h under argon atmosphere. Then, the reaction mixture was concentrated under reduced pressure before being purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=20/80) to obtain 200 mg of the intermediate silyl which is reacted with K.sub.2CO.sub.3 (351 mg, 2.4 eq.) in 15 ml of methanol. After 3 h stirring at room temperature, the solution is filtered through cotton. After evaporation to dryness, the crude is purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=30/70) to obtain the alkyne 41 as a brown solid 79% yield over 2 steps.

(265) This latter is reacted with the tosylated derivative 42 in the presence of K.sub.2CO3 in DMF. After 3 h at 80 C., the reaction mixture was cooled and 10 ml of H.sub.2O is introduced. The organic phase was extracted with ethyl acetate (310 ml). Then the organic phases are combined, dried with MgSO.sub.4 and filtered over cotton. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=15/85) to obtain the alkyne 39 in form of a colorless oil with a yield of 82%.

Example 24.2 2-{2-[4-(2-fluoroethoxy)phenyl]ethynyl}-1H-pyrrolo[2,3-b]pyridine 43

(266) ##STR00287##

(267) The compound was prepared according to procedure C1 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=30/70). Beige solid (38%), mp 250-252 C., Rf=0.20 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3122, 3054, 2978, 2883, 2790, 1603, 1582, 1534, 1498, 1277, 1249, 1175, 1078, 1051, 921. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.11 (s, 1H), 8.22 (s, 1H), 7.90 (d, J=7.9 Hz, 1H), 7.49 (d, J=8.6 Hz, 2H), 7.10-6.95 (m, 4H), 6.74 (s, 1H), 4.82 (t, J=6.2 Hz, 1H), 4.62 (t, J=6.2 Hz, 1H), 4.32 (t, J=5.7 Hz, 1H), 4.20 (t, J=5.7 Hz, 1H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 159.2 (Cq), 144.7 (CH), 133.5 (2CH), 128.7 (CH), 120.0 (Cq), 119.7 (Cq), 116.8 (CH), 115.6 (2CH), 114.4 (Cq), 106.2 (CH), 93.2 (Cq), 82.6 (d, J=151.0 Hz, CH.sub.2), 81.4 (Cq), 67.8 (d, J=18.8 Hz, CH.sub.2). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 222.2. HRMS (+ESI) calculated for C.sub.17H.sub.13FN.sub.2O (M+H+): 281.1084, found: 281.1085.

Example 25: 2-(2-{4-[(2-fluoroethoxy)methyl]phenyl}ethynyl)-1H-pyrrolo[2,3-b]pyridine 44

(268) 2-(2-{4-[(2-fluoroethoxy)methyl]phenyl}ethynyl)-1H-pyrrolo[2,3-b]pyridine 44 was synthesized in 2 steps. Initially, the corresponding alkyne 45 was prepared in one step and then we did the Sonogashira reaction with the azaindole to get the final compound.

Example 25.1 Synthesis of 1-ethynyl-4-((2-fluoroethoxy)methyl)benzene 45 (US2015/196672 A1)

(269) ##STR00288##

(270) Under argon, 100 mg of alkyne 46 (0.756 mmol, 1.0 eq.) is dissolved in 5 ml of DMF. At 0 C., 51 mg of NaH (50% in mineral oil, 1.06 mmol, 1.4 eq.) was added portionwise and after 5 minutes, 118 mg of mesyl 47 (0.832 mmol, 1.1 eq.) is added drop by drop. After 7 h at room temperature, 10 ml of H.sub.2O are added and the organic phase was extracted with ethyl acetate (310 ml). Then the organic phases are combined, dried and filtered over cotton. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=5/45) to obtain alkyne 45 as a colorless oil with a yield of 17%. .sup.1H NMR (250 MHz, CDCl.sub.3) 7.44 (d, J=8.2 Hz, 2H), 7.28 (d, J=8.2 Hz, 2H), 4.68-4.61 (m, 1H), 4.56 (s, 2H), 4.50-4.42 (m, 1H), 3.77-3.72 (m, 1H), 3.65-3.60 (m, 1H), 3.03 (s, 1H). CAS Number: 1562413-13-1.

Example 25.2 2-(2-{4-[(2-fluoroethoxy)methyl]phenyl}ethynyl)-1H-pyrrolo[2,3-b]pyridine 44

(271) ##STR00289##

(272) The compound was prepared according to procedure C1 and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=30/70). Yellow solid (57%), mp 192-194 C., Rf=0.18 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3122, 3054, 2978, 2883, 2790, 1603, 1582, 1534, 1498, 1277, 1249, 1175, 1078, 1051, 921. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 10.81 (s, 1H), 8.39 (s, 1H), 7.93 (s, 1H), 7.58 (s, 2H), 7.40 (s, 2H), 7.12 (s, 1H), 6.78 (s, 1H), 4.73-4.51 (m, 4H), 3.76 (d, J=29.5 Hz, 2H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 148.4 (Cq), 144.0 (CH), 138.8 (Cq), 131.7 (2CH), 129.1 (CH), 127.7 (2CH), 121.6 (Cq), 120.6 (Cq), 119.8 (Cq), 116.6 (CH), 106.6 (CH), 93.4 (Cq), 83.9 (d, J=169.4 Hz, CH.sub.2) 81.5 (Cq), 72.9 (CH.sub.2), 69.6 (d, J=19.7 Hz, CH.sub.2). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 221.4. HRMS (+ESI) calculated for C.sub.18H.sub.15FN.sub.2O (M+H+): 295.1241, found: 295.1242.

Example 26: 2-(2-{4-[2-(2-fluoroethoxy)ethoxyl]phenyl}ethynyl)-1H-pyrrolo[2,3-b]pyridine 48

(273) 2-(2-{4-[2-(2-fluoroethoxy)ethoxy]phenyl}ethynyl)-1H-pyrrolo[2,3-b]pyridine 48 was synthesized in 3 steps. Initially, the corresponding alkyne 49 was prepared in 2 steps from tosyl 50 and then we did the Sonogashira reaction with the azaindole to obtain the final compound.

Example 26.1 Synthesis of 1-ethynyl-4-[2-(2-fluoroethoxy)ethoxyl]benzene 49

(274) The alkyne 49 was obtained in three steps starting from ditosyl 50 which was prepared according to the method of Herbert (Organic Letters, 2013, 15, 13 p 3334-. 3337)

(275) ##STR00290##

Synthesis of Fluorinated 51

(276) Under argon, the compound 50 (300 mg, 0.724 mmol, 1.0 eq.) is dissolved in 17 ml of CH.sub.3CN. Then TBAF (0.796 ml, 0.796 mmol, 1.1 eq.) was added drop by drop. At the end of 1 h at 95 C., the reaction mixture was cooled to room temperature and evaporated under reduced pressure. The crude was purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=2/4) to obtain the fluorinated 51 as a colorless oil with a yield of 40%. .sup.1H NMR (400 MHz, CDCl.sub.3) 7.83 (d, J=8.3 Hz, 2H), 7.37 (d, J=8.3 Hz, 2H), 4.61-4.52 (m, 1H), 4.47-4.43 (m, 1H), 4.24-4.14 (m, 2H), 3.78-3.70 (m, 3H), 3.68-3.63 (m, 1H), 2.47 (s, 3H). CAS Number: 1118567-11-5

Synthesis of alkyne 49

(277) The alkyne 41 (43.4 mg, 0.367 mmol, 1.0 eq.) and the fluorinated 51 (107.0 mg, 0.408 mmol, 1.1 eq.) are placed in the presence of K.sub.2CO.sub.3 (101.3 mg, 0.734 mmol, 2.0 eq.) in 3 ml of DMF. After 3 h at 80 C., the reaction mixture was cooled and 10 ml of H.sub.2O is introduced. The organic phase was extracted with ethyl acetate (310 ml). Then the organic phases are combined, dried with MgSO4 and filtered through cotton. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=5/45) to give alkyne 49 as a colorless oil with a yield of 72%. Rf=0.65 (ethyl acetate/petroleum ether=20/80). IR (, cm1, neat) 3286, 2889, 2359, 2105, 1604, 1571, 1505, 1454, 1356, 1287, 1245, 1171, 1134, 1046, 927, 873. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.39 (d, J=8.8 Hz, 2H), 6.83 (d, J=8.8 Hz, 2H), 4.70-4.40 (m, 2H), 4.15-4.08 (m, 2H), 3.90-3.80 (m, 3H), 3.76-3.68 (m, 1H), 2.97 (s, 1H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 159.0 (Cq), 133.6 (2CH), 114.6 (2CH), 114.5 (Cq), 83.1 (d, J=169.1 Hz, CH.sub.2), 83.6 (Cq), 75.9 (CH), 70.6 (d, J=19.7 Hz, CH.sub.2), 69.8 (CH.sub.2), 67.5 (CH.sub.2). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) 223.0. HRMS (+ESI) calculated for C.sub.12H.sub.13FO.sub.2 (M+H+): 209.0972, found: 209.09714.

Example 26.2 2-(2-{4-[2-(2-fluoroethoxy)ethoxyl]phenyl}ethynyl)-1H-pyrrolo[2,3-b]pyridine 48

(278) ##STR00291##

(279) The compound was prepared according to procedure C1 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=10/90). yellowish solid (75%), mp 156-158 C., Rf=0.33 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3122, 3054, 2978, 2883, 2790, 1603, 1582, 1534, 1498, 1277, 1249, 1175, 1078, 1051, 92. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 9.97 (s, 1H), 8.35 (d, J=4.7 Hz, 1H), 7.90 (dd, J=7.8, 1.5 Hz, 1H), 7.51 (d, J=8.7 Hz, 2H), 7.10 (dd, J=7.9, 4.7 Hz, 1H), 6.94 (d, J=8.7 Hz, 2H), 6.73 (s, 1H), 4.73-4.47 (m, 2H), 4.19 (m, 2H), 3.92 (m, 3H), 3.83 (m, 2H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 159.6 (Cq), 148.7 (Cq), 144.4 (CH), 138.2 (Cq), 133.6 (2CH), 129.3 (CH), 120.5 (Cq) 116.9 (CH), 115.3 (2CH), 115.12 (Cq), 106.8 (CH), 92.8 (Cq), 83.7 (d, J=177.2 Hz, CH.sub.2), 80.7 (Cq), 71.1 (d, J=19.7 Hz, CH.sub.2), 70.4 (CH.sub.2), 67.7 (CH.sub.2). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) . 223.0. HRMS (+ESI) calculated for C.sub.19H.sub.17FN.sub.2O.sub.2 (M+H+): 325.1326, found: 325.1347.

Example 27. 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-benzyl-N-(2-fluoroethyl)aniline 52

(280) 4-((1H-pyrrolo[2,3-b] pyridin-2-yl) ethynyl)-N-benzyl-N-(2-fluoroethyl) aniline was synthesized in 5 steps from the benzylamine 54. initially, the corresponding alkyne 53 was prepared in 4 steps from the benzylamine 54 and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 27.1 Synthesis of N-benzyl-4-ethynyl-N-(2-fluoroethyl)aniline 53

(281) ##STR00292##

Synthesis of Amine 55

(282) Under argon, 130 mg of compound 42 (0.985 mmol, 1.0 eq.) is dissolved in 3 ml of CH.sub.3CN. After adding 0.40 ml of benzyl amine 54 (2.38 mmol, 4.0 eq.), the reaction mixture was heated at 90 C. for 12 h. After cooling the reaction mixture, 10 ml of a saturated solution of NaHCO.sub.3 is added. Then, the organic phase is extracted with DCM (310 ml). Then the organic phases are combined, dried with MgSO.sub.4 and filtered over cotton. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silica gel with eluting agent (methanol/dichloromethane/NH.sub.4OH=2/48/0.5) to afford the amine 55 as a colorless oil with a yield of 50%. .sup.1H NMR (250 MHz, CDCl.sub.3) 7.31 (m, 5H), 4.69-4.32 (m, 2H), 3.82 (s, 2H), 3.02-2.73 (m, 2H). CAS Number: 122974-04-3.

Synthesis of Amine 56

(283) Compound 56 was prepared according to procedure D and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether-1/49). Colorless oil (28%), Rf=0.50 (ethyl acetate/petroleum ether=5/45). IR (v, cm.sup.1, neat) 3028, 2951, 2359, 1591, 1493, 1451, 1386, 1352, 1228, 1193, 1173, 1101, 1080, 1046, 1003, 912, 882. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.39-7.19 (m, 7H), 6.66-6.57 (m, 2H), 4.71 (t, J=5.3 Hz, 1H), 4.66-4.55 (m, 3H), 3.76 (dt, J=23.5, 5.3 Hz, 2H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 147.25 (Cq), 137.89 (Cq), 131.9 (2CH), 128.7 (2CH), 127.09 (Cq), 126.4 (2CH), 114.2 (2CH), 108.9 (Cq), 81.6 (d, J=21.5 Hz, CH.sub.2), 55.0 (CH.sub.2), 51.3 (d, J=21.5 Hz, CH.sub.2). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) . 221.7. HRMS (+ESI) calculated for C.sub.15H.sub.15BrFN (M+H+): 308.0444, found: 308.0445.

Synthesis of Alkyne 53

(284) The alkyne 11 was prepared according to procedure E and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=2/48). Colorless oil (29% over two steps), Rf=0.50 (ethyl acetate/petroleum ether=2/48). IR (v, cm.sup.1, neat) 3028, 2951, 2359, 1591, 1493, 1451, 1386, 1352, 1228, 1193, 1173, 1101, 1080, 1046, 1003, 912, 882. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.37-7.10 (m, 7H), 6.68-6.54 (m, 2H), 4.62 (s, 2H), 4.61 (dt, J=47.1, 5.3 Hz, 2H), 3.74 (dt, J=23.3, 5.3 Hz, 2H), 2.93 (s, 1H), 4.76-4.58 (m, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 147.3 (Cq), 137.8 (Cq), 133.4 (2CH), 128.7 (2CH), 127.09 (Cq), 126.9 (2CH), 112.0 (2CH), 108.98 (Cq), 84.1 (Cq), 81.5 (d, J=21.5 Hz, CH.sub.2), 75.0 (CH), 54.0 (CH.sub.2), 50.9 (d, J=21.5 Hz, CH.sub.2). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 221.7. HRMS (+ESI) calculated for C.sub.17H.sub.16FN (M+H+): 254.1339, found: 254.1344.

Example 27.2 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-benzyl-N-(2-fluoroethyl)aniline 52

(285) ##STR00293##

(286) The compound was prepared according to procedure C1 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=30/70). Yellow solid (66%), mp 184-186 C., Rf=0.20 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3054, 2885, 2201, 1601, 1538, 1508, 1401, 1355, 1279, 1236, 1189, 1050, 811. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.06 (s, 1H), 8.23 (m, 1H), 7.91 (d, J=7.9 Hz, 1H), 7.42-7.25 (m, 3H), 7.23 (t, J=7.6 Hz, 2H), 7.07 (dd, J=7.6, 4.7 Hz, 1H), 6.82-6.64 (m, 2H), 4.70 (s, 1H), 4.66 (dt, J=47.8, 5.2 Hz, 3H), 3.85 (dt, J=25.5, 5.2 Hz, 2H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 150.5 (Cq), 148.5 (Cq), 144.2 (CH), 138.7 (Cq), 133.1 (2CH), 129.2 (2CH), 128.6 (CH), 127.5 (CH), 126.9 (2CH), 120.4 (Cq), 120.2 (Cq), 116.6 (CH), 112.8 (2CH), 108.4 (Cq), 105.2 (CH), 94.3 (Cq), 83.7 (Cq), 80.8 (d, J=168.8 Hz, CH.sub.2), 53.7 (CH.sub.2). .sup.19F NMR (235 MHz, DMSO-d.sub.6, 20 C.) . 221.7. HRMS (+ESI) calculated for C.sub.24H.sub.20FN.sub.3 (M+H+): 370.1714, found: 370.1413.

Example 28 N-(4-((1H-pyrrolo[2,3-b] pyridin-2-yl)ethynyl)phenyl)-N-(2-fluoroethyl)benzenesulfonamide 57

(287) N-(4-((1H-pyrrolo[2,3-b] pyridin-2-yl) ethynyl) phenyl)-N-(2-fluoroethyl) benzenesulfonamide 57 was synthesized in 3 steps from alkyne 59. Initially, the corresponding alkyne 58 was prepared in 2 steps and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 28.1 Synthesis of N-(4-ethynylphenyl)-N-(2-fluoroethyl)benzenesulfonamide 58

(288) The synthesis of alkyne 58 is obtained in two steps starting from alkyne 59. The alkyne 60 was prepared using the conditions of Sakai et al. (Macromolecules, 2012, 45, 20 from 8221 to 8227.7).

(289) ##STR00294##

Synthesis of Alkyne 60

(290) Under argon, alkyne 59 (100 mg, 0.854 mmol, 1.05 eq.) is dissolved in pyridine. At 0 C., benzenesulfonyl chloride (0.10 ml, 0.811 mmol, 1.0 eq.) is added dropwise. After 16 h at 0 C., 10 ml of a 1M HCl solution is added slowly. Then, the organic phase is extracted with ethyl acetate (310 ml). Then the organic phases are combined, dried with MgSO.sub.4 and filtered over cotton. After evaporation under reduced pressure, the alkyne 60 is obtained without purification in a yield of 96% as a yellowish solid. .sup.1H NMR (250 MHz, CDCl.sub.3) 7.83-7.73 (m, 2H), 7.58-7.31 (m, 5H), 7.02 (d, J=8.6 Hz, 2H), 6.57 (s1, 1H), 3.05 (s, 1H). CAS Number: 383147-75-9.

Synthesis of N-(4-ethynylphenyl)-N-(2-fluoroethyl) benzenesulfonamide 58

(291) The alkyne 60 (50.0 mg, 0.194 mmol, 1.0 eq.) and the fluorinated 42 (51 mg, 0.233 mmol, 1.2 eq.) are placed in the presence of K.sub.2CO.sub.3 (53.5 mg, 0.328 mmol, 2.0 eq.) in 2 ml of DMF. After 12 h at 80 C., the reaction mixture was cooled to room temperature. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silicagel eluting (ethyl acetate/petroleum ether=20/80) to give alkyne 58 as a colorless oil with a yield of 68%. Rf=0.50 (ethyl acetate/petroleum ether=20/80). IR (n, cm1, neat) 3285, 2959, 2360, 1601, 1500, 1446, 1347, 1265, 1228, 1164, 1080, 1046, 1017, 940, 903, 842. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.66-7.42 (m, 7H), 7.11-6.97 (m, 2H), 4.53 (dt, J=46.8, 5.3 Hz, 2H), 4.51-4.43 (m, 1H), 4.62-4.55 (m, 1H), 3.90 (dt, J=22.1, 5.3 Hz, 2H), 3.14 (s, 1H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 139.7 (Cq), 138.1 (Cq), 133.0 (3CH), 129.0 (2CH), 128.9 (2CH), 127.6 (2CH), 122.2 (Cq), 82.6 (Cq), 81.3 (d, J=172.4 Hz), 78.6 (CH), 51.1 (d, J=22.7 Hz). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) 223.0. HRMS (+ESI) calculated for C.sub.16H.sub.14FNO.sub.2S (M+H+): 304.0802, found: 304.0802.

Example 28.2 N-(4-((1H-pyrrolo[2,3-b] pyridin-2-yl)ethynyl)phenyl)-N-(2-fluoroethyl)benzenesulfonamide 57

(292) ##STR00295##

(293) The compound was prepared according to procedure C1 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=30/70). Yellow solid (51%), mp 202-204 C., Rf=0.33 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3124, 3058, 2962, 2890, 2358, 2219, 1581, 1537, 1496, 1446, 1329, 1286, 1229, 1155, 1123, 1084, 1050, 1017, 956, 937, 912, 836, 808, 762. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.25 (s, 1H), 8.32-8.27 (m, 1H), 7.98 (d, J=7.9 Hz, 1H), 7.75-7.71 (m, 1H), 7.64-7.60 (m, 4H), 7.57 (d, J=8.2 Hz, 2H), 7.17 (d, J=8.2 Hz, 2H), 7.14-7.09 (m, 1H), 6.85 (s, 1H), 4.53-4.48 (m, 1H), 4.42-4.37 (m, 1H), 4.01-3.97 (m, 1H), 3.93 (m, 1H). .sup.13C NMR (63 MHz, DMSO-d.sub.6 20 C.) 206.9 (Cq), 148.8 (Cq), 145.1 (CH), 139.7 (Cq), 137.9 (Cq), 133.9 (CH), 132.5 (2CH), 129.9 (2CH), 129.3 (CH), 129.02 (2CH), 127.7 (CH), 121.6 (CH), 119.9 (Cq), 119.1 (Cq), 116.9 (CH), 107.0 (CH), 92.34 (Cq), 83.7 (Cq), 81.7 (d, J=168.8 Hz, CH.sub.2), 51.0 (d, J=20.2 Hz, CH.sub.2), .sup.19F NMR (235 MHz, DMSO-d.sub.6, 20 C.) . 222.0. HRMS (+ESI) calculated for C.sub.23H.sub.18FN.sub.3O.sub.2S (M+H+): 420.1176, found: 420.1174.

Example 29 2-((4-(((3-fluorobenzyl)oxy)methyl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 61

(294) 2-((4-(((3-fluorobenzyl)oxy)methyl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine was synthesized in 2 steps from the alkyne 46. Initially, the corresponding alkyne 62 was prepared in one step, and then we made the Sonogashira reaction with azaindole to obtain the final compound.

Example 29.1 Synthesis of 1-(((4-ethynylbenzyl)oxy)methyl)-3-fluorobenzene 62

(295) ##STR00296##

(296) Under argon, 100 mg of alkyne 46 (0.756 mmol, 1.1 eq.) is dissolved in 2 mL of DMF. At 0 C., 48 mg of NaH (50% in mineral oil, 1.02 mmol, 1.5 eq.) was added portionwise, then after 1 h at room temperature, 0.084 ml bromine 63 (0.68 mmol, 1.0 eq.) is added drop by drop. After 20 h at room temperature, 10 ml of H.sub.2O is added and the organic phase was extracted with ethyl acetate (310 ml). Then the organic phases are combined, dried and filtered over cotton. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silica gel eluting (ethyl acetate/petroleum ether=2/48) to obtain 93 mg of the alkyne 62 as a colorless oil with a yield of 52%. Rf=0.80 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3291, 2858, 1698, 1607, 1590, 1507, 1487, 1449, 1412, 1359, 1267, 1204, 1174, 1138, 1094, 1070, 1017, 946, 859. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.49 (d, J=7.9 Hz, 2H), 7.32 (d, J=7.9 Hz, 3H), 7.10 (m, 2H), 6.99 (m, 1H), 4.55 (2s, 4H), 3.07 (s, 1H). .sup.13C NMR (63 MHz, CDCl.sub.3 20 C.) 162.4 (d, J=246.4 Hz, Cq), 140.7 (d, J=7.9 Hz, Cq), 138.8 (Cq), 132.2 (2CH), 129.9 (d, J=7.9 Hz, CH), 127.5 (2CH), 123.0 (d, J=2.9 Hz, CH), 121.45 (Cq), 114.6 (d, J=12.8 Hz, CH), 114.38 (d, J=12.8 Hz, CH), 83.5 (Cq), 77.2 (CH), 71.8 (CH.sub.2), 71.5 (d, J=2.0 Hz, CH.sub.2). .sup.19F NMR (235 MHz, DMSO-d.sub.6, 20 C.) . 113.4. HRMS (+ESI) calculated for C.sub.16H.sub.13FO (M+H.sup.+): 241.1023, found: 241.1024.

Example 29.2 2-((4-(((3-fluorobenzyl)ox)methyl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 61

(297) ##STR00297##

(298) The compound was prepared according to procedure C1 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=30/70). Yellow solid (58%), mp 192-194 C., Rf=0.20 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3057, 2978, 2893, 2848, 1607, 1584, 1488, 1447, 1433, 1406, 1357, 1282, 1258, 1205, 1141, 1111, 1062, 1007, 934. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.23 (s, 1H), 8.29 (s, 1H), 7.97 (d, J=9.8 Hz, 1H), 7.58 (s, 2H), 7.46 (d, J=7.9 Hz, 3H), 7.20 (m, 2H), 7.12 (d, J=7.9 Hz, 2H), 6.84 (s, 1H), 4.60 (s, 4H). .sup.13C NMR (63 MHz, DMSO-d.sub.6 20 C.) 160.6 (d, J=276 Hz, Cq), 148.81 (Cq), 144.9 (CH), 141.8 (d, J=8.3 Hz, Cq), 139.9 (Cq), 131.8 (2CH), 130.8 (d, J=8.3 Hz, CH), 128.9 (CH), 128.2 (2CH), 123.8 (d, J=2 Hz, CH), 121.1 (Cq), 119.9 (Cq), 119.4 (Cq), 116.8 (CH), 114.7 (d, J=20.9 Hz, CH), 114.4 (d, J=20.9 Hz, CH), 106.8 (CH), 93.1 (Cq), 82.6 (Cq), 71.5 (CH.sub.2), 71.3 (d, J=2 Hz, CH.sub.2). .sup.19F NMR (235 MHz, DMSO-d.sub.6, 20 C.) . 113.4. HRMS (+ESI) calculated for C.sub.23H.sub.17FN.sub.2O (M+H.sup.+) 357.1397, found: 357.1398.

Example 30. 4-[4-[2-(5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl] phenyl]morpholine 64

(299) 4-[4-[2-(5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl]phenyl]morpholine was synthesized in 4 steps from dibromobenzene. Initially, the corresponding alkyne 65 was prepared in 3 steps and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 30.1 Preparation of 4-(4-ethynylphenyl)morpholine 65

(300) ##STR00298##

Synthesis Bromine 66

(301) Compound 66 was prepared according to procedure D and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=1/49). Colorless oil (97%). .sup.1H NMR (250 MHz, CDCl.sub.3) 7.40-7.22 (m, 2H), 6.82-6.68 (m, 2H), 3.90-3.72 (m, 4H), 3.17-3.03 (m, 4H). CAS Number: 30483-75-1.

Synthesis of True Alkyne 65

(302) The alkyne 65 was prepared according to procedure E and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=2/48). Colorless oil (68% over two steps). .sup.1H NMR (250 MHz, CDCl.sub.3) 7.47-7.38 (m, 4H), 6.88-6.80 (m, 4H), 3.91-3.84 (m, 4H), 3.25-3.18 (m, 4H), 3.01 (s, 1H). CAS Number: 41876-72-6.

Example 30.2 4-[4-[2-(5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl]phenyl]morpholine 64

(303) ##STR00299##

(304) The compound was prepared according to procedure C1 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=40/60). Yellow solid (42%), mp>260 C., Rf=0.33 (ethyl acetate/petroleum ether=40/60). IR (v, cm.sup.1, neat) 3114, 3057, 2964, 2852, 2209, 1604, 1586, 1536, 1507, 1448, 1394, 1381, 1341, 1285, 1264, 1242, 1222, 1197, 1157, 1122, 1053, 922. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.26 (s, 1H), 8.23 (s, 1H), 7.81 (m, 1H), 7.43 (d, J=8.7 Hz, 2H), 6.99 (d, J=8.7 Hz, 2H), 6.73 (s, 1H), 3.85-3.58 (m, 4H), 3.24-3.04 (m, 4H). .sup.13C NMR (63 MHz, DMSO-d.sub.6 20 C.) 155.8 (d, J=239.2 Hz, Cq), 151.64 (Cq), 145.61 (Cq), 132.9 (2CH), 132.7 (d, J=29.0 Hz, CH), 122.6 (Cq), 120.6 (d, J=7.5 Hz, Cq), 114.9 (2CH), 113.8 (d, J=20.9 Hz, CH), 110.9 (Cq), 105.8 (d, J=4.4 Hz, CH), 94.8 (Cq), 80.6 (Cq), 66.4 (2CH.sub.2), 47.7 (2CH.sub.2). .sup.19F NMR (235 MHz, DMSO-d.sub.6, 20 C.) . 138.4. HRMS (+ESI) calculated for C.sub.19H.sub.16FN.sub.3O (M+H+): 322.1350, found: 322.1354.

Example 31. N-(4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)benzyl)-2-fluoro-N-methylethan-1-amine 67

(305) N-(4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)benzyl)-2-fluoro-N-methylethan-1-amine was synthesized in 2 steps from the alkyne 69. Initially, the corresponding alkyne 68 was prepared in one step and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 31.1 Synthesis of N-[(4-ethynylphenyl)methyl]-2-fluoro-N-methyl-ethanamine 68

(306) ##STR00300##

(307) Under argon, 100 mg of aldehyde 69 (0.77 mmol, 1.0 eq.) and 98.5 mg of amine 70 (0.845 mmol, 1.1 eq.) are dissolved in 5 ml of THF. After the addition of 0.536 ml of DIPEA (3.08 mmol, 4.0 eq.) and 386.4 mg of NaBH (OAc).sub.3, the reaction mixture was stirred for 12 h at room temperature. Then 15 ml of a saturated solution of NaHCO.sub.3 is added and the organic phase was extracted with ethyl acetate (315 ml). Then the organic phases are combined, dried and filtered over cotton. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=5/45) to obtain 95 mg of the alkyne 68 as a colorless oil with a yield of 65%, Rf=0.40 (ethyl acetate/petroleum ether=5/45). IR (v, cm.sup.1, neat) 3289, 2952, 2794, 2359, 2107, 1682, 1504, 1455, 1410, 1364, 1017, 846, 825. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.40 (d, J=8.2 Hz, 2H), 7.24 (d, J=8.2 Hz, 2H), 4.51 (dt, J=47.6, 5.0 Hz, 2H), 3.53 (s, 2H), 3.01 (s, 1H), 2.68 (dt, J=27.0, 5.0 Hz, 2H), 2.25 (s, 3H). .sup.13C NMR (63 MHz, CDCl.sub.3 20 C.) 139.8 (Cq), 132.1 (2CH), 128.8 (2CH), 120.8 (Cq), 83.8 (Cq), 82.4 (d, J=158.6 Hz, CH.sub.2), 76.45 (CH), 62.3 (CH.sub.2), 56.8 (d, J=20.1 Hz, CH.sub.2), 42.7 (CH.sub.3). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) . 219.2. HRMS (+ESI) calculated for C.sub.12H.sub.14FN (M+H+): 192.1183, found: 192.1185.

Example 31.2 N-(4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)benzyl)-2-fluoro-N-methylethan-1-amine 67

(308) ##STR00301##

(309) The compound was prepared according to procedure C1 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=40/60). Yellow solid (60%), mp 160-162 C., Rf=0.18 (ethyl acetate/petroleum ether=40/60). IR (v, cm.sup.1, neat) 3055, 2951, 2779, 1583, 1536, 1497, 1433, 1405, 1359, 1283, 1115, 1014, 879. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 11.78 (s, 1H), 8.41 (m, 1H), 7.93 (m, 1H), 7.56 (d, J=8.0 Hz, 2H), 7.38 (d, J=8.0 Hz, 2H), 7.20-7.05 (m, 1H), 6.78 (s, 1H), 4.58 (dt, J=47.6, 5.0 Hz, 2H), 3.62 (s, 2H), 2.76 (dt, J=27.1, 5.0 Hz, 2H), 2.33 (s, 3H). .sup.13C NMR (63 MHz, CDCl.sub.3 20 C.) 148.6 (Cq), 143.6 (CH), 139.9 (Cq), 131.5 (2CH), 129.1 (2CH), 121.1 (Cq), 120.8 (Cq), 120.1 (Cq), 116.5 (CH), 106.3 (CH), 93.4 (Cq), 83.8 (Cq), 82.5 (d, J=167.6 Hz, CH.sub.2), 62.3 (CH.sub.2), 57.8 (d, J=20.0 Hz, CH.sub.2), 42.7 (CH.sub.3). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) . 219.1. HRMS (+ESI) calculated for C.sub.19H.sub.18FN.sub.3 (M+H+): 308.1557, found: 308.1557.

Example 32. 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylbenzamide 71

(310) 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylbenzamide was synthesized in 2 steps from the alkyne 73. Initially the corresponding alkyne 72 was prepared in one step and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 32.1 Synthesis of 4-ethynyl-N-(2-fluoroethyl)-N-methyl-benzamide 72

(311) ##STR00302##

(312) Under argon, 100 mg of the acid 73 (0.684 mmol, 1.0 eq.) and 85 mg of amine 70 (0.752 mmol, 1.1 eq.) are dissolved in 5 ml of DMF. After the addition of 0.571 ml of DIPEA (3.28 mmol, 4.8 eq.) and 312 mg of HATU (0.821 mmol, 1.2 eq.), the reaction mixture was stirred for 12 h at room temperature.

(313) Then, 15 ml of H.sub.2O is added and the organic phase was extracted with ethyl acetate (315 ml). Then the organic phases are combined, dried and filtered over cotton. After evaporation under reduced pressure, the crude was purified by flash chromatography column on silica gel with eluting agent (ethyl acetate/petroleum ether=30/70) to obtain 95 mg of the alkyne 72 as a colorless oil with a yield of 83%. Rf=0.25 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3290, 3225, 2929, 2359, 1625, 1508, 1482, 1400, 1303, 1177, 1074, 1036, 1017, 979, 847, 764, 668. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.53 (d, J=7.9 Hz, 2H), 7.38 (d, J=7.2 Hz, 2H), 4.60 (m, 2H), 3.92-3.46 (m, 2H), 3.11 (m, 4H). .sup.13C NMR (63 MHz, CDCl.sub.3 20 C.) 168.9 (Cq), 136.2 (Cq), 132.2 (2CH), 127.0 (2CH), 123.6 (Cq), 83.8 (d, J=167.6 Hz, CH.sub.2), 82.8 (Cq), 78.6 (CH), 48.4 (d, J=20 Hz, CH.sub.2), 39.4 (CH.sub.3). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) . 222.2. HRMS (+ESI) calculated for C.sub.12H.sub.12FN (M+H+): 206.0975, found: 206.0976.

Example 32.2 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylbenzamide

(314) ##STR00303##

(315) The compound was prepared according to procedure C1 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=10/90). Yellow solid (34%), mp 192-194 C., Rf=0.33 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3055, 2951, 2779, 1583, 1536, 1497, 1433, 1405, 1359, 1283, 1115, 1014, 879. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.40 (d, J=4.7 Hz, 1H), 7.95 (d, J=7.8 Hz, 1H), 7.63 (d, J=7.9 Hz, 2H), 7.47 (d, J=7.9 Hz, 2H), 7.13 (dd, J=7.8, 4.7 Hz, 1H), 6.81 (s, 1H), 4.74 (d, J=47.8 Hz, 2H), 3.86 (d, J=28.1 Hz, 2H), 3.13 (s, 3H). .sup.13C NMR DEPT (63 MHz, CDCl.sub.3 20 C.) 144.2 (CH), 131.6 (2CH), 129.2 (CH), 127.3 (2CH), 116.7 (CH), 107.1 (CH), 84.8 (d, J=167.6 Hz, CH.sub.2), 83.0 (Cq), 48.6 (d, J=20.0 Hz, CH.sub.2), 39.6 (CH.sub.3). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) . 222.5. HRMS (+ESI) calculated for C.sub.19H.sub.16FN.sub.3O (M+H+): 322.1350, found: 322.1352.

Example 33. 3-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 74

(316) 3-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline was synthesized in 3 steps from 3-bromoaniline. Initially, the corresponding alkyne 75 was prepared in 2 steps and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 33.1 Synthesis of 3-ethynyl-N,N-dimethylaniline 75

(317) To synthesize the alkyne 75, we use the method of Fang et coll. (Journal of Chemical Research, 2015, 39, 8, 487-491)

(318) ##STR00304##

(319) The catalyst [Pd(PPh.sub.3).sub.4] (29 mg, 0.025 mmol, 5 mol %) was added to a degassed solution of bromine derivative 3-bromo-N,N-dimthylaniline (100 mg, 0.5 mmol, 1.0 eq.), of ethynyltrimethylsilane (0.083 ml, 0.6 mmol, 1.2 eq), CuI (5 mg, 0.025 mmol, 5 mol %) in a mixture of diisopropylamine/toluene (1:3) at a concentration of 0.1 M. The mixture was heated at 80 C. for 16 h under argon. After returning to room temperature, the mixture was concentrated under reduced pressure before being purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=1/49) to obtain 100 mg of the intermediate alkyne as a colorless oil with quantitative yield. This latter is reacted with K.sub.2CO.sub.3 (103 mg, 0.745, 1.5 eq.) in methanol. After 3 h stirring at room temperature, the solvent was evaporated. Then, the crude is solubilized in ethyl acetate OML. Then the organic phase is washed with brine (10 ml). Then the organic phase is dried with MgSO.sub.4, filtered through cotton and evaporated under reduced pressure. The alkyne 75 is obtained with a yield of 64% without purification. .sup.1H NMR (250 MHz, CDCl.sub.3) 7.22-7.11 (m, 1H), 6.93-6.82 (m, 2H), 6.72 (m, 1H), 3.48 (s, 6H), 3.3 (s, 1H). CAS Number: 52324-05-7.

Example 33.2 3-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 74

(320) ##STR00305##

(321) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (DCM=100). White solid (27%), mp 226-228 C., Rf=0.25 (dichloromethane=100). IR (, cm.sup.1, neat) 3063, 2890, 2805, 1595, 1494, 1360, 1343, 1296, 1224, 1143, 767. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 11.91 (s, 1H), 7.83 (dd, J=2.8, 1.8 Hz, 1H), 7.41 (dd, J=8.0, 2.8 Hz, 1H), 6.82 (t, J=8.0 Hz, 1H), 6.48-6.32 (m, 4H), 2.50 (s, 6H). .sup.13C NMR (63 MHz, DMSO-d.sub.6 20 C.) 155.8 (d, J=239.5 Hz, Cq), 150.7 (Cq), 145.6 (Cq), 133.1 (d, J=29.2 Hz, CH), 129.9 (CH), 122.1 (d, J=17.9 Hz, Cq), 120.1 (d, J=7.5 Hz, Cq), 119.4 (CH), 114.8 (CH), 114.1 (d, J=20.8 Hz, CH), 113.9 (CH), 106.5 (d, J=4.5 Hz, CH), 94.9 (Cq), 81.1 (Cq), 40.5 (2CH.sub.3). .sup.19F NMR (235 MHz, DMSO-d.sub.6, 20 C.) . 138.5. HRMS (+ESI) calculated for C.sub.17H.sub.14FN.sub.3 (M+H+): 280.1244, found: 280.1245.

Example 34 2-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 76

(322) 2-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline was synthesized in 4 steps from 2-iodoaniline. Initially, the corresponding alkyne 77 was prepared in 3 steps and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 34.1 Synthesis of 2-ethynyl-N,N-dimethylaniline 77

(323) ##STR00306##

(324) 500 mg of 2-iodoaniline (2.28 mmol, 1.0 eq.) is dissolved in 10 ml of CH.sub.3CN. Then 0.425 ml of iodomethane (6.84 mmol, 3.0 eq.) and 787 mg of K.sub.2CO.sub.3 (5.7 mmol, 2.5 eq.) are added successively. After 16 h at reflux, the reaction mixture is cooled. 20 ml of H.sub.2O was added and the organic phase is extracted with ethyl acetate (315 ml). Then the organic phases are combined, dried and filtered over cotton. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=2/48) to obtain 434 mg of the iodated 78 with 2% monoalkylated.

Synthesis of 2-ethynyl-N,N-dimethylaniline 77

(325) The catalyst [Pd(PPh.sub.3).sub.4] (12 mg, 0.018 mmol, 1.0 mol %) was added to a degassed solution of iodine derivative 78, (434 mg, 1.75 mmol, 1.0 eq.), ethynyltrimethylsilane (0.365 ml, 2.6 mmol, 1.5 eq.), CuI (10 mg, 0.052 mmol, 3 mol %) and Et.sub.3N (0.240 ml, 1.75 mmol, 1.0 eq.) in 1.5 ml of DMF. The mixture was stirred at room temperature for 16 h under argon. Then the mixture is concentrated under reduced pressure before being purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=1/49) to obtain 186 mg of the intermediate alkyne as a colorless oil with the yield of 50%. This latter is reacted with K.sub.2CO.sub.3 (177 mg, 1.28 mmol, 1.5 eq.) in 15 ml of methanol. After stirring for 3 h at room temperature, the solvent was evaporated. Then, the crude is dissolved in 10 ml of ethyl acetate. Then the organic phase is washed with brine (310 ml). Then the organic phase is dried, filtered through cotton and evaporated under reduced pressure. The alkyne 77 was obtained with the yield of 64% without purification. .sup.1H NMR (250 MHz, CDCl.sub.3) 7.43 (m, 1H), 7.29-7.13 (m, 1H), 6.95-6.76 (m, 2H), 3.43 (s, 1H), 2.90 (s, 6H). CAS Number: 219605-52-4.

Example 34.2 2-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 76

(326) ##STR00307##

(327) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=10/90). White solid (27%), mp 146-148 C., Rf=0.30 (ethyl acetate/petroleum ether=15/85). IR (, cm.sup.1, neat) 3058, 2837, 2789, 2203, 1588, 1533, 1504, 1487, 1451, 1430, 1397, 1345, 1322, 1291, 1272, 1189, 1113, 1046, 983, 943. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 10.73 (s, 1H), 8.32 (t, J=2.3 Hz, 1H), 7.59 (ddd, J=28.4, 8.2, 2.3 Hz, 2H), 7.38-7.29 (m, 1H), 7.04-6.92 (m, 2H), 6.75 (d, J=2.0 Hz, 1H), 3.04 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3 20 C.) 155.9 (d, J=241.8 Hz, Cq), 155.2 (Cq), 145.1 (Cq), 134.3 (CH) 132.4 (d, J=29.2 Hz, CH), 130.1 (CH), 122.6 (Cq), 120.7 (d, J=7.3 Hz, Cq), 120.6 (CH) 117.1 (CH), 114.8 (Cq), 114.2 (d, J=20.8 Hz, CH), 105.8 (d, J=4.5 Hz, CH), 93.8 (Cq), 86.2 (Cq), 43.6. (2CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 138.5. HRMS (+ESI) calculated for C.sub.17H.sub.14FN.sub.3 (M+H+): 280.1244, found: 280.1245.

Example 35 1-[4-[2-(5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl]phenyl]pyrrolidin-2-one 79

(328) 1-[4-[2-(5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl]phenyl]pyrrolidin-2-one was synthesized in 3 steps. Initially, the corresponding alkyne 80 was prepared in 3 steps and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 35.1 Synthesis of 1-(4-ethynylphenyl)pyrrolidin-2-one 80

(329) ##STR00308##

Synthesis of Bromine 82

(330) CuI (12 mg, 0.282 mmol, 20 mol %) was added to a degassed solution of iodine derivative 81 (200 mg, 0.707 mmol, 1.0 eq.), amine 83 (0.056 ml, 0.742 mmol, 1.5 eq.), N,N-dimethylethylenediamine (0.026 ml, 0.282 mmol, 20% mol) and CsCO.sub.3 (459 mg, 1.41 mmol, 2.0 eq) in 3.0 ml of CH.sub.3CN. The mixture was stirred at 80 C. for 16 h under argon. Then the mixture was cooled and filtered through Celite.

(331) The filtrate is evaporated under reduced pressure before being purified by flash column chromatography on silicagel with eluting agent (ethyl acetate/petroleum ether=25/75) to give 110 mg of the bromine 82 as a colorless oil with the yield of 65%. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.57-7.37 (m, 4H), 3.81 (t, J=7.0 Hz, 2H), 2.58 (t, J=8.1 Hz, 2H), 2.14 (m, 2H). CAS Number: 7661-32-7.

Synthesis of 1-(4-ethynylphenyl)pyrrolidin-2-one 80

(332) Under argon, Pd(PPh.sub.3).sub.4 (24 mg, 0.021 mmol, 0.1 eq.) and CuI (4 mg, 0.021 mmol, 0.01 eq.) were added to a degassed solution of Et.sub.3N (1 ml) containing ethynyltrimethylsilane (0.058 ml, 0.416 mmol, 2.0 eq.) and the bromine derivative 82 (50 mg, 0.21 mmol, 1.0 eq.). After 16 h at 60 C., the solvent was evaporated under reduced pressure. Then, the reaction mixture was purified by flash column chromatography on silicagel. Then, 56 mg of the intermediate alkyne was reacted with K.sub.2CO.sub.3 (45 mg, 0.217 mmol, 1.5 eq.) in 5 ml of methanol. After 3 h at room temperature, the solvent was evaporated under reduced pressure. The crude product was dissolved in 10 ml of ethyl acetate. Then the organic phase is washed with brine (310 ml). Then the organic phase is dried with MgSO.sub.4, filtered through cotton and evaporated under reduced pressure to obtain alkyne 80 with a yield of 67% as a white solid. mp 136-138 C., Rf=0.5 (ethyl acetate/petroleum ether=50/50). IR (, cm.sup.1, neat) 3292, 3031, 2915, 2099, 1605, 1514, 1494, 1451, 1395, 1355, 1233, 1177, 1100, 1046, 1003, 912, 883, 847, 815. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.60 (d, J=9.0 Hz, 2H), 7.48 (d, J=9.0 Hz, 2H), 3.86 (dd, J=7.4, 6.7 Hz, 2H), 3.33 (s, 1H), 2.69-2.55 (m, 2H), 2.25-2.08 (m, 2H). .sup.13C NMR (63 MHz, CDCl.sub.3 20 C.) 174.8 (Cq), 140.3 (Cq), 133.2 (2CH), 119.7 (2CH), 118.2 (Cq), 83.4 (Cq), 77.3 (CH), 46.9 (CH.sub.2), 33.27 (CH.sub.2), 18.37 (CH.sub.2). HRMS (+ESI) calculated for C.sub.12H.sub.12NO (M+H+): 186.0913, found: 186.0913.

Example 35.2 1-[4-[2-(5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl]phenyl]pyrrolidin-2-one 79

(333) ##STR00309##

(334) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=10/90). White solid (27%), mp 256-258 C., Rf=0.30 (ethyl acetate/petroleum ether=15/85). IR (, cm.sup.1, neat) 3058, 2837, 2789, 2203, 1588, 1533, 1504, 1487, 1451, 1430, 1397, 1345, 1322, 1291, 1272, 1189, 1113, 1046, 983, 943. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.37 (s, 1H), 8.27 (s, 1H), 7.85 (d, J=9.8 Hz, 1H), 7.79 (d, J=7.4 Hz, 2H), 7.60 (d, J=7.4 Hz, 2H), 6.81 (s, 1H), 3.87 (m, 2H), 2.54 (m, 2H), 2.07 (m, 2H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 174.8 (Cq), 155.7 (d, J=240 Hz, Cq), 145.6 (Cq), 140.8 (Cq), 133.3 (d, J=28.9 Hz, CH), 132.4 (2CH), 121.9 (Cq), 120.2 (d, J=7.5 Hz, Cq), 119.5 (2CH), 116.6 (Cq), 114.1 (d, J=20.8 Hz, CH), 106.5 (d, J=3.5 Hz, Cq), 93.8 (Cq), 81.8 (Cq), 48.4 (CH.sub.2), 32.9 (CH.sub.2), 17.8 (CH.sub.2). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 138.5. HRMS (+ESI) calculated for C.sub.19H.sub.14FN.sub.3O (M+H+): 320.1192, found: 320.1193.

Example 36. 2-[2-(2-fluorophenyl)ethynyl]-1H-pyrrolo[2,3-b]pyridine 84

(335) ##STR00310##

(336) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=10/90). Yellowish solid (32%), mp 210-212 C., Rf=0.20 (ethyl acetate/petroleum ether=15/85). IR (, cm.sup.1, neat) 3058, 2837, 2789, 2203, 1588, 1533, 1504, 1487, 1451, 1430, 1397, 1345, 1322, 1291, 1272, 1189, 1113, 1046, 983, 943. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 11.55 (s, 1H), 8.46 (s, 1H), 7.95 (d, J=7.9 Hz, 1H), 7.59 (t, J=7.3 Hz, 1H), 7.43-7.34 (m, 1H), 7.17 (m, 3H), 6.83 (s, 1H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 163.7 (d, J=252.5 Hz, Cq), 148.5 (Cq), 144.1 (CH), 133.3 (CH), 130.5 (d, J=7.9 Hz, CH), 129.2 (CH), 124.1 (CH), 120.6 (Cq), 119.5 (Cq), 116.6 (CH), 115.7 (d, J=20.5 Hz, CH), 111.3 (d, J=15.2 Hz, Cq), 106.9 (CH), 86.8 (d, J=15.2 Hz, Cq). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 109.3. HRMS (+ESI) calculated for C.sub.15H.sub.9FN.sub.2 (M+H+): 237.0822, found: 237.0823.

Example 37. 2-((4-(1-(3-fluoropropyl)piperidin-4-yl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 85

(337) 2-((4-(1-(3-fluoropropyl)piperidin-4-yl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine was synthesized in 4 steps. Initially, the corresponding alkyne 86 was prepared in 3 steps and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 37.1 Synthesis of 4-(4-ethynylphenyl)-1-(3-fluoropropyl)piperidine 86

(338) ##STR00311##

Synthesis of 4-(4-bromophenyl)-1-(3-fluoropropyl) piperidine 89

(339) The bromine 87 (176 mg, 0.635 mmol, 1.2 eq.) and the fluorine 88 (123 mg, 0.529 mmol, 1.0 eq.) are placed in the presence of K.sub.2CO.sub.3 (219 mg, 0.1.59 mmol, 3.0 eq.) in 10 ml of CH.sub.3CN. After 18 h at 90 C., the reaction mixture was cooled to room temperature and the solvent was evaporated under reduced pressure. The crude product is dissolved in 10 ml of ethyl acetate. Then the organic phase was washed with brine (310 ml). Then the organic phase is dried, filtered through cotton and evaporated under reduced pressure. After purification on silica gel with an eluent (ethyl acetate/petroleum ether Et.sub.3N), the bromine 89 was obtained with a yield of 58% in form of a colorless oil. Rf=0.2 (methanol/dichloromethane=2/48). IR (, cm.sup.1, neat) 3305, 2925, 1639, 1512, 1441, 1376, 1258, 1171, 1124, 1039, 997, 911, 835. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.41 (d, J=8.4 Hz, 2H), 7.10 (d, J=8.4 Hz, 2H), 4.62 (t, J=6.0 Hz, 1H), 4.43 (t, J=6.0 Hz, 1H), 3.23-2.93 (m, 2H), 2.59-2.43 (m, 2H), 2.24-1.60 (m, 10H). .sup.13C NMR (63 MHz, CDCl.sub.3 20 C.) 145.3 (Cq), 131.4 (2CH), 128.6 (2CH), 119.7 (Cq), 82.7 (d, J=164.3 Hz, CH.sub.2), 54.7 (d, J=5.4 Hz, CH.sub.2), 54.3 (CH.sub.2), 42.2 (CH.sub.2), 33.4 (CH.sub.2), 28.0 (d, J=19.6 Hz, CH.sub.2). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) . 220. HRMS (+ESI) calculated for C.sub.14H.sub.19BrFN (M+H+): 300.0757, found: 300.0757.

Synthesis of 4-(4-ethynylphenyl)-1-(3-fluoropropyl)piperidine 86

(340) The alkyne 86 was prepared according to procedure E and purified by flash column chromatography on silica gel (methanol/dichloromethane=2/48) but containing 20% of the bromine 89.

Example 37.2 2-((4-(1-(3-fluoropropyl)piperidin-4-yl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine

(341) ##STR00312##

(342) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (methanol/dichloromethane/NH.sub.4OH=2/48/0.5). White solid (55%), mp 218-220 C., Rf=0.20 (methanol/dichloromethane/NH.sub.4OH=2/48/0.5). IR (, cm.sup.1, neat) 3052, 2936, 2777, 2360, 1583, 1534, 1495, 1466, 1432, 1404, 1376, 1356, 1325, 1284, 1133, 1111, 1041, 999, 981, 938, 917, 828, 801, 763. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.19 (s, 1H), 8.28 (d, J=4.6 Hz, 1H), 7.96 (d, J=8.0 Hz, 1H), 7.51 (d, J=7.8 Hz, 2H), 7.35 (d, J=8.0 Hz, 2H), 7.10 (dd, J=7.9, 4.7 Hz, 1H), 6.81 (d, J=1.9 Hz, 1H), 4.56 (t, J=6.0 Hz, 1H), 4.44 (t, J=5.9 Hz, 1H), 2.98 (m, 2H), 2.50 (m, 2H), 2.41 (m, 2H), 2.02 (m, 2H), 1.92-1.59 (m, 6H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 148.8 (Cq), 148.1 (Cq), 144.9 (CH), 131.8 (2CH), 128.8 (CH), 127.8 (2CH), 120.0 (Cq), 119.7 (CH), 119.5 (Cq), 116.8 (Cq), 106.6 (CH), 93.3 (Cq), 82.9 (d, J=161.5 Hz, CH.sub.2), 82.2 (Cq), 54.3 (d, J=6.0 Hz, CH.sub.2), 54.1 (2CH.sub.2), 40.8 (CH.sub.2), 33.2 (2CH.sub.2), 28.0 (d, J=19.1 Hz, CH.sub.2). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 218.3. HRMS (+ESI) calculated for C.sub.23H.sub.24FN.sub.3 (M+H+): 361.2027, found: 361.2026.

Example 38. 5-fluoro-2-((4-(4-phenylpiperidin-1-yl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 90

(343) 5-fluoro-2-((4-(4-phenylpiperidin-1-yl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine was synthesized in 4 steps. Initially, the corresponding alkyne 91 was prepared in 3 steps and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 38.1 Synthesis of 1-(4-ethynylphenyl)-4-phenyl-piperidine 91

(344) ##STR00313##

Synthesis of bromine 92

(345) Compound 92 was prepared according to procedure D and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=2/48). White solid (97%). .sup.1H NMR (250 MHz, CDCl.sub.3) 7.41-7.20 (m, 6H), 6.92-6.83 (m, 2H), 3.84-3.74 (m, 2H), 2.84 (m, 2H), 2.68 (m, 1H), 2.03-1.83 (m, 4H). CAS Number: 303975-64-6.

Synthesis of 1-(4-ethynylphenyl)-4-phenyl-piperidine 91

(346) The alkyne 91 was prepared according to procedure E and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=2/48). White solid (76%), mp 136-138 C., Rf=0.30 (ethyl acetate/petroleum ether=2/48). IR (, cm.sup.1, neat) 3157, 3072, 2893, 2205, 1605, 1541, 1511, 1432, 1273, 1224, 1183, 809, 763, 507. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.46-7.30 (m, 4H), 7.32-7.20 (m, 3H), 6.95-6.87 (m, 2H), 3.96-3.85 (m, 2H), 3.01 (s, 1H), 2.90 (m, 2H), 2.71 (m, 1H), 2.03-1.81 (m, 4H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 151.5 (Cq), 145.8 (Cq), 133.2 (2CH), 128.5 (2CH), 126.8 (2CH), 126.4 (CH), 115.4 (2CH), 111.5 (Cq), 84.4 (Cq), 75.3 (CH), 49.5 (2CH.sub.2), 42.5 (CH), 32.9 (2CH.sub.2). HRMS (+ESI) calculated for C.sub.19H.sub.19N (M+H+): 262.1590, found: 292.1590.

Example 38.2 5-fluoro-2-((4-(4-phenylpiperidin-1-yl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine

(347) ##STR00314##

(348) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=20/80). White solid (34%), mp>260 C., Rf=0.20 (ethyl acetate/petroleum ether=20/80). IR (, cm.sup.1, neat) 3117, 3063, 2917, 2813, 2734, 2205, 1600, 1586, 1534, 1503, 1462, 1386, 1341, 1292, 1214, 1191, 1154, 1101, 1011, 819. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.22 (s, 1H), 8.19 (m, 1H), 7.79 (m, 1H), 7.47-7.09 (m, 7H), 6.99 (d, J=8.8 Hz, 2H), 6.68 (s, 1H), 3.95 (m, 2H), 2.80 (m, 3H), 1.90-1.55 (m, 4H). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 138.5. HRMS (+ESI) calculated for C.sub.26H.sub.22FN.sub.3 (M+H+): 396.1868, found: 396.1869.

Example 39. 5-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-2-fluoro-N,N-dimethylaniline 93

(349) 5-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-2-fluoro-N,N-dimethylaniline was synthesized in 4 steps. Initially, the corresponding alkyne 94 was prepared in 3 steps and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 39.1 Synthesis of 5-ethynyl-2-fluoro-N,N-dimethyl-aniline 94

(350) ##STR00315##

Synthesis of Bromine 96

(351) Bromine 95 (1.0 g, 5.26 mmol, 1.0 eq.) is dissolved in 0.650 ml of trimethyl phosphate (5.52 mmol, 1.05 eq.). After 2 h30 at 200 C., the mixture was cooled to room temperature and 15 ml of a solution of 2M NaOH was added. After one night at room temperature, the organic phase is extracted with dichloromethane (315 ml). Then the organic phases are combined, dried and filtered over cotton. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=2/48) to obtain the compound 96. Colorless oil (61%). 1H NMR (250 MHz, CDCl.sub.3) 7.01-6.77 (m, 3H), 2.84 (s, 6H). CAS Number: 1352214-46-0.

Synthesis of 5-ethynyl-2-fluoro-N,N-dimethylaniline 94

(352) The catalyst [Pd(PPh.sub.3).sub.4] (53 mg, 0.046 mmol, 5 mol %) was added to a degassed solution of bromine derivative 96 (200 mg, 0.92 mmol, 1.0 eq.), ethynyltrimethylsilane (0.152 ml, 0.1 1 mmol, 1.2 eq), CuI (9 mg, 0.046 mmol, 5 mol %) in a mixture of diisopropylamine/toluene (1:3) at a concentration of 0.1 M. The mixture was heated at 80 C. for 16 h under argon. After returning to room temperature, the mixture was concentrated under reduced pressure before being purified by flash column chromatography on silica gel with eluting agent (ethyl acetate/petroleum ether=2/48) to obtain 172 mg of the intermediate alkyne. This latter is reacted with K.sub.2CO.sub.3 (151 mg, 1.1 mmol, 1.5 eq.) in methanol. After stirring for 3 h at room temperature, the solvent was evaporated. Then, the crude is solubilized in 10 ml of ethyl acetate. Then the organic phase is washed with brine (310 ml). Then the organic phase is dried with MgSO.sub.4, filtered through cotton and evaporated under reduced pressure.

(353) The crude was purified by flash column chromatography on silica gel with eluent (ethyl acetate/petroleum ether=2/48) to afford the alkyne 94. Colorless oil (33%). Rf=0.30 (ethyl acetate/petroleum ether=15/85). IR (, cm.sup.1, neat) 3290, 2970, 2930, 2853, 2102, 1606, 1511, 1463, 1434, 1356, 1336, 1273, 1245, 1227, 1185, 1140, 1023, 935. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.12-6.81 (m, 3H), 3.00 (s, 1H), 2.84 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 155.3 (d, J=249.4 Hz, Cq), 140.7 (d, J=9.4 Hz, Cq), 125.0 (d, J=8.2 Hz, CH), 121.9 (d, J=4.2 Hz, CH), 118.1 (d, J=3.8 Hz, Cq), 116.3 (d, J=22.2 Hz, CH), 83.4 (Cq), 76.1 (CH), 42.6 (d, J=4.2 Hz, 2CH.sub.3).sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 119.7. HRMS (+ESI) calculated for C.sub.10H.sub.10FN (M+H+): 164.0870, found: 164.0872.

Example 39.2 Synthesis of 5-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-2-fluoro-N,N-dimethylaniline 93

(354) ##STR00316##

(355) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=45/55). Yellowish solid (79%), mp 170-172 C., Rf=0.20 (ethyl acetate/petroleum ether=30/70). IR (, cm.sup.1, neat) 3157, 3072, 2893, 2205, 1605, 1541, 1511, 1432, 1273, 1224, 1183, 809, 763, 507. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 10.84 (s, 1H), 8.43-8.31 (m, 1H), 7.93 (d, J=7.9 Hz, 1H), 7.10 (d, J=7.9 Hz, 2H), 7.05-6.93 (m, 1H), 6.76 (s, 1H), 2.90 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 155.3 (d, J=249.9 Hz, Cq), 148.4 (Cq), 143.9 (CH), 140.9 (d, J=9.4 Hz, Cq), 128.9 (CH), 124.5 (d, J=8.2 Hz, CH), 121.3 (d, J=4.2 Hz, CH), 120.7 (Cq), 119.82 (Cq), 118.5 (Cq), 116.6 (CH), 116.5 (d, J=22.2 Hz, CH), 106.4 (CH), 93.2 (Cq), 80.5 (Cq), 42.7 (CH.sub.3), 42.6 (CH.sub.3).sub.1.sup.9F NMR (376 MHz, CDCl.sub.3, 20 C.) . 119.3. HRMS (+ESI) calculated for C.sub.17H.sub.14FN.sub.3 (M+H+): 280.1244, found: 280.1244.

Example 40. 2-((4-(4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2

(356) yl)ethynyl)phenoxy)phenyl)(methyl)amino)ethan-1-ol 97 2-((4-(4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenoxy)phenyl)(methyl)amino)ethan-1-ol 97 was synthesized in 6 steps. Initially, the corresponding alkyne 98 was prepared in 4 steps starting from the phenyl ether 99 and then we performed the Sonogashira reaction with azaindole followed by a deprotection reaction with TBAF to obtain the final compound.

Example 40.1 Synthesis of N-[2-[tert-butyl(diphenyl)silyl]oxoethyl]-4-(4-ethynylphenoxy)-N-methyl-aniline 98

(357) ##STR00317##

Synthesis of Iodine 100

(358) Under argon, 200 mg of phenyl ether 99 (1.18 mmol, 1.0 eq.) is dissolved in 5 ml of CH.sub.3CN. 528 mg of N-iodosuccinimide (2.35 mmol, 2.0 eq.) and 10 L of TFA are added. After 4 h at reflux, the reaction mixture was cooled to room temperature and 10 ml of sodium thiosulfate solution is added followed by 10 ml of DCM. Then the organic phase was washed with sodium thiosulfate solution (310 ml). Then the organic phase was dried with MgSO.sub.4, filtered through cotton and evaporated under reduced pressure. The crude product is triturated with diethyl ether, followed by vacuum filtration. The iodine 100 is obtained as a white solid with a yield of 30%. .sup.1H NMR (250 MHz, CDCl.sub.3) 7.70-7.49 (m, 4H), 6.87-6.65 (m, 4H). CAS Number: 28896-49-3.

Synthesis of Compound 101

(359) Under argon, Pd.sub.2dba.sub.3 (0.05 eq.) and tBu.sub.3P (0.075 mmol) were added to a degassed anhydrous toluene solution of 0.3M concentration containing the amine (1.0 eq.), the iodine 100 (1.0 eq.) and t-BuONa (1.2 eq.). After 24 h at room temperature, the solvent was evaporated under reduced pressure. Then, the reaction mixture was concentrated under reduced pressure, before being purified by flash column chromatography on silica gel. The compound 101 is obtained as a colorless oil in 33% yield, Rf=0.20 (ethyl acetate/petroleum ether=1/49). IR (, cm.sup.1, neat) 2928, 2856, 1610, 1508, 1477, 1426, 1390, 1273, 1232, 1163, 1105, 1056, 1003, 928, 866, 818. 781. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.65 (dt, J=7.8, 1.3 Hz, 4H), 7.53 (d, J=8.5 Hz, 2H), 7.45-7.33 (m, 6H), 6.85 (d, J=9.0 Hz, 2H), 6.72-6.61 (m, 2H), 6.55 (d, J=9.0 Hz, 2H), 3.81 (t, J=6.2 Hz, 2H), 3.47 (t, J=6.2 Hz, 2H), 2.93 (s, 3H), 1.04 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 159.4 (Cq), 146.5 (Cq), 145.7 (Cq), 138.3 (2CH), 135.6 (4CH), 133.4 (Cq), 129.7 (4CH), 127.7 (2CH), 121.2 (2CH), 119.1 (2CH), 112.8 (2CH), 84.0 (Cq), 61.1 (CH.sub.2), 54.9 (CH.sub.2), 39.3 (CH.sub.3), 26.8 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.31H.sub.34INO.sub.2Si (M+H+): 608.1476, found: 608.1474.

Synthesis N-(2-((tert-butyldiphenylsilyl)ox)ethyl)-4-(4-ethylnlphenoxy)-N-methylaniline 98

(360) Catalyst [Pd(PPh.sub.3).sub.2Cl.sub.2] (2.8 mg, 0.004 mmol, 0.03 eq.) was added to a degassed solution of iodine 101 (80 mg, 0.131 mmol, 1.0 eq.), ethynyltrimethylsilane (0.027 ml, 0.2 mmol, 1.5 eq.), CuI (1 mg, 0.004 mmol, 0.03 eq.), in the Et.sub.3N at a concentration of 0.3 M. The mixture was stirred at 85 C. for 4 h under argon atmosphere. Then the reaction mixture was concentrated under reduced pressure, before being purified by column flash chromatography on silica gel with eluent (ethyl acetate/petroleum ether=20/80) to obtain 70 mg of the intermediate which reacted with K.sub.2CO.sub.3 (25 mg, 0.181 mmol, 1.5 eq.) in 6 ml of DCM/methanol (1/1). After 3 h stirring at room temperature, the solution is filtered through cotton. After evaporation to dryness, the crude is purified by flash chromatography column on silica gel with eluting agent (ethyl acetate/petroleum ether=30/70) to give alkyne 98 as a brown solid with a yield of 69% yield over 2 steps. mp 170-172 C., Rf=0.20 (ethyl acetate/petroleum ether=30/70). IR (, cm.sup.1, neat) 3284, 3070, 2929, 2856, 1610, 1513, 1495, 1471, 1427, 1360, 1280, 1234, 1160, 1103, 985, 927, 869. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.65-7.56 (m, 4H), 7.41-7.28 (m, 8H), 6.82 (m, 4H), 6.62-6.45 (m, 2H), 3.87-3.64 (t, J=6.2 Hz, 2H), 3.44 (t, J=6.2 Hz, 2H), 2.97 (s, 1H), 2.91 (s, 3H), 1.01 (s, 9H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 160.2 (2Cq), 147.2 (Cq), 146.2 (Cq), 136.3 (4CH), 134.2 (2CH), 134.1 (Cq), 130.4 (2CH), 128.4 (4CH), 122.0 (2CH), 117.2 (2CH), 115.8 (Cq), 113.5 (2CH), 77.9 (Cq) 76.6 (CH), 61.8 (CH.sub.2), 55.5 (CH.sub.2), 39.9 (Cq), 27.5 (3CH.sub.3), 19.7 (CH.sub.3). HRMS (+ESI) calculated for C.sub.33H.sub.35NO.sub.2Si (M+H+): 506.2009, found: 506.2009.

Example 40.2 2-((4-(4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenoxy)phenyl) (methyl)amino)ethan-1-ol 97

(361) ##STR00318##

(362) The compound was prepared according to procedure C2 followed by procedure F and purified by flash column chromatography on silica gel (methanol/dichlorometliane=2/48). Yellowish solid (76% over 2 steps), mp 172-174 C., Rf=0.20 (methanol/dichloromethane=2/48). IR (, cm.sup.1, neat) 3122, 2925, 1662, 1610, 1510, 1494, 1436, 1399, 1349, 1296, 1246, 1165, 1120, 1048, 984, 872, 839. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.34 (s, 1H), 8.26 (s, 1H), 7.83 (m, 1H), 7.57 (m, 2H), 7.03-6.86 (m, 4H), 6.75 (m, 3H), 4.72-4.60 (t, J=5.9 Hz, 1H), 3.56 (q, J=5.9 Hz, 2H), 3.39 (t, J=6.1 Hz, 2H), 2.93 (s, 3H). .sup.13C NMR (101 MHz, DMSO-d.sub.6 20 C.) 155.3 (d, J=239.2 Hz, Cq), 147.9 (Cq), 147.2 (Cq), 145.6 (Cq), 144.9 (Cq), 133.7 (2CH), 132.8 (d, J=20.9 Hz, CH) 122.1 (Cq), 121.9 (2CH), 120.2 (d, J=6.2 Hz, Cq), 117.0 (2CH), 114.9 (Cq), 114.0 (d, J=20.2 Hz, CH), 113.3 (2CH), 106.4 (d, J=4.0 Hz, CH), 93.7 (Cq), 81.2 (Cq), 58.6 (CH.sub.2), 55.1 (CH.sub.2), 39.2 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 138.4. HRMS (+ESI) calculated for C.sub.24H.sub.20FN.sub.3O.sub.2 (M+H+): 402.1612, found: 402.1611.

Example 41. 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-2-fluoro-N,N-dimethylaniline 103

(363) 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-2-fluoro-N,N-dimethylaniline was synthesized in 4 steps. Initially, the corresponding alkyne 104 was prepared in 3 steps from aldehyde 105 and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 41.1 Synthesis of 5-ethynyl-2-fluoro-N,N-dimethylaniline 104

(364) ##STR00319##

Synthesis of Aldehyde 106

(365) Under argon, the aldehyde 105 (500 mg, 3.52 mmol, 1.0 eq.) was dissolved in 3 ml of DMSO. Then, TBAB (567 mg, 1.76 mmol, 0.5 eq.), K.sub.2CO.sub.3 (486 mg, 3.52 mmol, 1.0 eq.) and dimethylamine (C=2M, 8.8 ml, 17.6 mmol, 5.0 eq.) were added successively. After 7 h at 90 C., 10 ml of a saturated solution of NaHCO.sub.3 is added. The organic phase are extracted with ethyl acetate (310 ml) then they are combined, dried with MgSO.sub.4 and filtered through cotton. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silica gel with eluent (ethyl acetate/petroleum ether=30/70) to give the aldehyde 106 as a colorless oil with a yield of 92%. .sup.1H NMR (250 MHz, CDCl.sub.3) 9.72 (s, 1H), 7.57-7.38 (m, 2H), 6.78 (m, 1H), 3.02 (s, 6H). CAS Number: 1021240-69-6.

Synthesis of 5-ethynyl-2-fluoro-N,N-dimethyl-aniline 104

(366) Under argon, CBr.sub.4 (198 mg, 0.6 mmol, 1.0 eq.) is dissolved in 5 ml of DCM. At 0 C., PPh.sub.3 (315 mg, 1.2 mmol, 2.0 eq.) was added in one portion. After 10 minutes, the aldehyde 106 (100 mg, 0.6 mmol, 1.0 eq.) was dissolved in 5 ml of DCM and then added dropwise. After 40 minutes at 0 C., 10 ml of H.sub.2O is added. The organic phase was extracted with ethyl acetate (310 ml) and was then combined, dried with MgSO.sub.4 and filtered through cotton. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silica gel with eluent (ethyl acetate/petroleum ether=10/40) to obtain compound 107 as a white solid with a yield of 52%. Then, it was reacted with TBAF, 3H.sub.2O (780 mg, 2.47 mmol, 8.0 eq.) in a mixture of THF/H.sub.2O (2 ml/0.1 ml). After 7 h at 90 C., the mixture was cooled to room temperature and 5 ml of H.sub.2O was added. The organic phase was extracted with ethyl acetate (310 ml) and was then combined, dried with MgSO.sub.4 and filtered over cotton. After evaporation under reduced pressure, the crude was purified by flash column chromatography on silica gel with eluent (ethyl acetate/petroleum ether=1/99) to obtain the alkyne 104 as a yellow oil with a yield of 30%. Rf=0.50 (ethyl acetate/ether=1/99 petiole). IR (, cm.sup.1, neat) 3290, 2970, 2930, 2853, 2102, 1606, 1511, 1463, 1434, 1356, 1336, 1273, 1245, 1227, 1185, 1140, 1023, 935. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.22-7.09 (m, 2H), 6.81-6.69 (m, 1H), 3.00 (s, 1H), 2.89 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 153.5 (d, J=245.3 Hz, Cq), 141.4 (d, J=8.4 Hz, Cq) 128.6 (d, J=3.0 Hz, CH) 119.7 (d, J=23.1 Hz, CH), 117.4 (d, J=4.5 Hz, CH), 113.3 (d, J=9.2 Hz, Cq), 83.0 (d, J=2.7 Hz, Cq), 76.23 (CH), 42.4 (CH.sub.3), 42.4 (CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 122.4. HRMS (+ESI) calculated for C10H10FN (M+H+): 164.0870, found: 164.0872.

Example 41.2 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-2-fluoro-N,N-dimethylaniline 103

(367) ##STR00320##

(368) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=45/55). Yellowish solid (79%), mp 180-182 C., Rf=0.20 (ethyl acetate/petroleum ether=30/70). IR (, cm.sup.1, neat) 3157, 3072, 2893, 2205, 1605, 1541, 1511, 1432, 1273, 1224, 1183, 809, 763, 507. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.15 (s, 1H), 8.27 (s, 1H), 7.95 (d, J=7.8 Hz, 1H), 7.46-7.20 (m, 2H), 7.20-7.03 (m, 1H), 6.96 (t, J=9.0 Hz, 1H), 6.78 (s, 1H), 2.89 (s, 6H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 152.9 (d, J=243.9 Hz, Cq), 148.5 (Cq), 144.5 (CH), 141.2 (d, J=8.0 Hz, Cq), 128.6 (m, 2CH), 120.2 (Cq), 119.8 (Cq), 119.6 (d, J=22.8 Hz, CH), 118.2 (d, J=4.7 Hz, CH), 116.6 (CH), 112.2 (d, J=9.7 Hz, Cq), 106.0 (CH), 92.5 (Cq), 81.5 (Cq), 42.2 (CH.sub.3), 42.1 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 122.1. HRMS (+ESI) calculated for C17H14FN3 (M+H+): 280.1244, found: 280.1245.

Example 42: 2-((4-(1H-pyrazol-1-yl)phenyl)ethynyl)-5-fluoro-1H-pyrrolo[2,3-b]pyridine 108

(369) 2-((4-(1H-pyrazol-1-yl)phenyl)ethynyl)-5-fluoro-1H-pyrrolo[2,3-b]pyridine was synthesized in 4 steps. Initially, the corresponding alkyne 109 was prepared in 3 steps from the compound 110 and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 42.1 Synthesis of 1-(4-ethynylphenyl)-1H-pyrazole 109

(370) ##STR00321##

Synthesis of Bromine 112

(371) CuI (27 mg, 0.141 mmol, 20 mol %) was added to a degassed solution of iodine derivative 110 (200 mg, 0.707 mmol, 1.0 eq.), of amine 111 (50.5 mg, 0.742 mmol, 1.05 eq.), N,N-dimethylethylenediamine (0.026 ml, 0.282 mmol, 20% mol) and CsCO.sub.3 (459 mg, 1.41 mmol, 2.0 eq.) in 3.0 ml of CH.sub.3CN. The mixture was stirred at 80 C. for 16 h under argon. Then the mixture was cooled and filtered through Celite. The filtrate is evaporated under reduced pressure before being purified by flash column chromatography on silica gel with eluent (ethyl acetate/petroleum ether=25/75) to obtain 115 mg of the bromine 112 in the form of a colorless oil with a yield of 73% yield. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.86 (m, 1H), 7.69 (m, 1H), 7.55 (m, 4H), 6.45 (m, 1H). Numro CAS Number: 13788-92-6.

Synthesis of 1-(4-ethynylphenyl)-1H-pyrazole 109

(372) Under argon, Pd(PPh.sub.3).sub.2Cl.sub.2 (6 mg, 0.009 mmol, 0.04 eq.) and CuI (2 mg, 0.009 mmol, 0.04 eq.) were added to a degassed solution of Et.sub.3N/Dioxane (1.5 ml (2/1)) containing ethynyltrimethylsilane (0.155 ml, 1.12 mmol, 5.0 eq.), the bromine derivative 112 (50 mg, 0.224 mmol, 1.0 eq.). After 16 h at 100 C., the solvent was evaporated under reduced pressure. Then, the reaction mixture was purified by flash column chromatography on silica gel. Then, 20 mg of the intermediate alkyne is reacted with K.sub.2CO.sub.3 (17 mg, 0.125 mmol, 1.5 eq.) in 3 ml of methanol. After 3 h at room temperature, the solvent was evaporated under reduced pressure. The crude product is dissolved in 10 ml of ethyl acetate. Then the organic phase is washed with brine (310 ml). Then the organic phase is dried with MgSO.sub.4, filtered through cotton and evaporated under reduced pressure to obtain the alkyne 109 as a white solid with a yield of 37% over 2 steps. mp 54-56 C., Rf=0.5 (ethyl acetate/petroleum ether=2/48). IR (, cm.sup.1, neat) 3273, 3232, 3150, 2918, 1606, 1521, 1506, 1390, 1335, 1312, 1248, 1205, 1193, 1205, 1193, 1118, 1045, 1028, 934. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.90 (dd, J=2.5, 0.6 Hz, 1H), 7.71 (dd, J=1.8, 0.6 Hz, 1H), 7.65 (d, J=8.9 Hz, 2H), 7.55 (d, J=8.9 Hz, 2H), 6.45 (dd, J=2.5, 1.8 Hz, 1H), 3.09 (s, 1H). .sup.13C NMR (63 MHz, CDCl.sub.3 20 C.) 141.5 (CH), 140.1 (Cq), 133.3 (2CH), 126.7 (CH), 120.0 (Cq), 118.7 (2CH), 108.1 (CH), 82.9 (Cq), 77.9 (CH). HRMS (+ESI) calculated for C.sub.11H.sub.9N.sub.2 (M+H+): 169.0760, found: 169.0763.

Example 42.2 2-((4-(1H-pyrazol-1-yl)phenyl)ethynyl)-5-fluoro-1H-pyrrolo[2,3-b]pyridine 108

(373) ##STR00322##

(374) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=10/40). Yellowish solid (51%), mp>260 C., Rf=0.1 (ethyl acetate/petroleum ether=10/40). IR (v, cm.sup.1, neat) 3157, 3072, 2893, 2205, 1605, 1541, 1511, 1432, 1273, 1224, 1183, 809, 763, 507. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.41 (s, 1H), 8.60 (d, J=2.6 Hz, 1H), 8.36-8.21 (m, 1H), 7.96 (d, J=8.7 Hz, 1H), 7.90-7.79 (m, 2H), 7.71 (d, J=8.7 Hz, 2H), 6.84 (d, J=1.9 Hz, 1H), 6.5 (s, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 155.7 (d, J=240.5 Hz, Cq), 145.7 (Cq), 142.1 (CH), 140.3 (Cq), 133.3 (d, J=29.0 Hz, CH), 133.1 (2CH), 128.5 (CH), 121.6 (Cq), 120.1 (d, J=7.5 Hz, Cq), 119.3 (Cq), 118.9 (2CH), 114.2 (d, J=20.7 Hz, CH), 108.9 (CH), 106.8 (d, J=4.6 Hz, CH), 93.2 (Cq), 82.7 (Cq). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 122.1. HRMS (+ESI) calculated for C.sub.18H.sub.11FN.sub.4 (M+H+): 303.1040, found: 303.1039.

Example 43. 2-[2-[4-(4-fluoro-1-piperidyl)phenyl]ethynyl]-1H-pyrrolo[2,3-b]pyridine 113

(375) 2-[2-[4-(4-fluoro-1-piperidyl)phenyl]ethynyl]-1H-pyrrolo[2,3-b]pyridine 113 was synthesized in 4 steps. Initially, the corresponding alkyne 114 was prepared in 3 steps from dibromobenzene and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 43.1 Synthesis of 1-(4-ethynylphenyl)-4-fluoropiperidine 114

(376) ##STR00323##

Synthesis of Bromine 115

(377) Compound 115 was prepared according to procedure D and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=1/49). Colorless oil (32%). .sup.1H MNR (250 MHz, CDCl.sub.3) 7.33 (d, J=8.9 Hz, 2H), 6.80 (d, J=8.9 Hz, 2H), 4.97-4.61 (m, 1H), 3.41-3.22 (m, 2H), 3.25-3.08 (m, 2H), 2.14-1.86 (m, 4H). CAS Number: 1423130-86-2.

Synthesis of 1-(4-ethynylphenyl)-4-fluoro-piperidine 114

(378) The alkyne 114 was prepared according to procedure E and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=2/48). Colorless oil (36% over two steps). IR (v, cm.sup.1, neat) 3291, 2962, 2930, 2853, 2102, 1606, 1511, 1463, 1434, 1373, 1356, 1336, 1273, 1245, 1227, 1185, 1141, 1093, 1023, 935. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.40 (d, J=8.8 Hz, 2H), 6.87 (d, J=8.8 Hz, 2H), 4.85 (m, 1H), 3.51-3.37 (m, 2H), 3.34-3.20 (m, 2H), 3.01 (s, 1H), 2.15-1.88 (m, 4H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 150.9 (Cq), 133.3 (2CH), 115.4 (2CH), 111.9 (Cq), 88.1 (d, J=171.3 Hz, CH), 84.2 (Cq), 75.4 (CH), 44.9 (CH.sub.2), 44.9 (CH.sub.2), 30.9 (CH.sub.2), 30.7 (CH.sub.2). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 181.4. HRMS (+ESI) calculated for C.sub.13H.sub.14FN (M+H+): 204.1183, found: 204.1181.

Example 43.2 2-[2-[4-(4-fluoro-1-piperidyl)phenyl]ethynyl]-1H-pyrrolo[2,3-b]pyridine 113

(379) ##STR00324##

(380) The compound was prepared according to procedure C1 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=30/70). Yellow solid (quantitative), mp>260 C., Rf=0.20 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3113, 3057, 2955, 2932, 2819, 2207, 1600, 1584, 1533, 1505, 1405, 1370, 1354, 1278, 1224, 1189, 1027, 816. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.05 (s, 1H), 8.21 (s, 1H), 7.91 (d, J=7.8 Hz, 1H), 7.38 (d, J=8.6 Hz, 2H), 7.09 (m, 1H), 6.98 (d, J=8.6 Hz, 2H), 6.69 (s, 1H), 4.99-4.76 (m, 2H), 3.49 (dt, J=13.5, 5.4 Hz, 2H), 3.33 (dt, J=13.5, 5.4 Hz, 2H), 2.02 (m, 4H). .sup.13C NMR DEPT (63 MHz, DMSO-d.sub.6, 20 C.) 144.4 (CH), 132.9 (2CH), 128.5 (CH), 116.7 (CH), 115.3 (2CH), 105.8 (CH), 88.8 (d, J=169.2 Hz, CH), 44.4 (d, J=6.8 Hz, 2CH.sub.2), 30.8 (d, J=19.1 Hz, 2CH.sub.2). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) . 181.5. HRMS (+ESI) calculated for C.sub.20H.sub.18FN.sub.3 (M+H+): 320.1157, found: 320.1557.

Example 44. 4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethyl-[1,1-biphenyl]-4-amine 116

(381) 4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethyl-[1,1-biphenyl]-4-amine was synthesized in 4 steps. Initially, the corresponding alkyne 117 was prepared in 3 steps from the compound 119 and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 44.1 Synthesis of 4-ethynyl-N,N-dimethyl-[1,1-biphenyl]-4-amine 117

(382) ##STR00325##

Synthesis of Bromine 118

(383) Under argon, Pd(OAc).sub.2 (0.05 eq.) and Xantphos (0.067 mmol) were added to a degassed anhydrous toluene solution of 0.3M concentration containing dimethylamine hydrochloride (1.0 eq.), The bromine 119 (2.0 eq.) and Cs.sub.2C0.sub.3 (3.0 eq.). After 16 h at 100 C., the solvent was evaporated under reduced pressure. Then, the reaction mixture was concentrated under reduced pressure before being purified by flash column chromatography on silica gel to obtain the bromine 118 as a white solid with a yield of 68%. .sup.1H NMR (250 MHz, CDCl.sub.3) 7.51-7.34 (m, 6H), 6.76 (d, J=8.9 Hz, 2H), 2.97 (s, 6H). CAS Number: 92194-03-1.

Synthesis of 4-(4-ethynylphenyl)-N,N-dimethyl-aniline 117

(384) The alkyne 117 was prepared according to procedure E and at a temperature of 60 C. and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=2/48). Colorless oil (67% over two steps). .sup.1H NMR (250 MHz, CDCl.sub.3) 7.56-7.34 (m, 6H), 6.84-6.67 (m, 2H), 3.31 (s, 1H), 2.97 (s, 6H). CAS Number: 1190376-40-9.

Example 44.2 4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethyl-[1,1-biphenyl]-4-amine 116

(385) ##STR00326##

(386) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=30/70). Yellow solid (quantitative), mp>260 C., Rf=0.20 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3428, 3157, 3072, 2893, 2205, 1605, 1541, 1511, 1432, 1273, 1224, 1183, 809, 763, 507. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.38 (s, 1H), 8.28 (s, 1H), 7.86 (dd, J=9.4, 2.7 Hz, 1H), 7.71 (d, J=8.1 Hz, 2H), 7.63-7.53 (m, 4H), 6.86-6.75 (m, 3H), 2.97 (s, 6H). .sup.13C NMR DEPT (63 MHz, DMSO-d.sub.6 20 C.) 133.1 (d, J=29 Hz, CH), 132.3 (2CH), 127.6 (2CH), 126.0 (2CH), 114.1 (d, J=20.8 Hz, CH), 113.03 (2CH), 106.6 (d, J=4.8 Hz, CH), 40.9 (2CH3). .sup.19F NMR (235 MHz, DMSO-d.sub.6, 20 C.) . 138.5. HRMS (+ESI) calculated for C.sub.23H.sub.18FN.sub.3 (M+H+): 356.1557, found: 356.1554.

Example 45. (5-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)furan-2-yl)methanol 120

(387) (5-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)furan-2-yl)methanol was synthesized in 4 steps. Initially, the corresponding alkyne 121 was prepared in 3 steps from the compound 122 and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 45.1 Preparation du (5-ethenylfuran-2-yl)methanol 121

(388) The alkyne 121 was prepared in three steps starting with 2-bromo-2-furaldehyde 122. The first step has been described in Organometallics, (Vol. 24, No. 4, 2005, p. 693) and the last step was found in the patent (US2010/63041 A1 p. 30)

(389) ##STR00327##

Synthesis of the Aldehyde 123

(390) The compound 123 was prepared according to procedure G. Brown oil (99%), Rf=0.5 (ethyl acetate/petroleum ether=2/98). CAS Number: 153026-71-2.

Synthesis of (5-ethenylfuran-2-yl) methanol 121

(391) 100 mg of aldehyde 123 (0.83 mmol, 1.0 eq.) is dissolved with NaBH.sub.4 (14 mg, 0.37 mmol, 0.45 eq.) in 2.5 ml of ethanol. After 20 min at 0 C., 10 ml of H.sub.2O is added and the organic phase was extracted with ethyl acetate (310 ml). The organic phases are combined, dried over MgSO.sub.4, filtered through cotton and evaporated under reduced pressure. The alkyne 121 was obtained in the form of a brown oil with a yield of 99%. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 6.47 (dd, J=3.3, 0.7 Hz, 1H), 6.15 (dd, J=3.3, 0.7 Hz, 1H), 4.45 (s, 2H,), 3.32 (s, 1H). CAS Number: 153026-89-2.

Example 45.2 (5-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)furan-2-yl)methanol 120

(392) ##STR00328##

(393) The compound was obtained according to procedure C2 and purified by flash column chromatography on silica gel (methanol/dichloromethane/NH.sub.4OH=4/94/2). Yellow solid (30%). mp: 216 C. Rf=0.42 (methanol/dichloromethane/NH.sub.4OH=4/94/2). IR (v, cm.sup.1, neat) 3200, 3059, 2975, 2884, 2206, 1586, 1506, 1401, 1299, 1277, 1158, 1112, 1022, 982, 873. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.46 (s, 1H), 8.41-8.18 (m, 1H), 7.87 (dd, J=9.3, 2.7 Hz, 1H), 6.94 (d, J=3.4 Hz, 1H), 6.88 (d, J=1.9 Hz, 1H), 6.45 (d, J=3.3 Hz, 1H), 5.39 (t, J=5.8 Hz, 1H), 4.40 (d, J=5.8 Hz, 2H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 159.9 (d, J=249.9 Hz, Cq), 146.1 (Cq), 145.1 (Cq), 134.6 (CH), 133.8 (Cq), 133.6 (Cq), 120.5 (Cq), 118.2 (CH), 114.2 (d, J=20.6 Hz, CH), 109.0 (CH), 107.5 (d, J=4.5 Hz, CH), 87.8 (Cq), 84.4 (Cq), 58.5 (CH.sub.2). .sup.19F NMR (235 MHz, DMSO-d.sub.6, 20 C.) 138.16. HRMS (+ESI) calculated for C.sub.14H.sub.9FN.sub.2O.sub.2 (M+H+): 257.0720, found: 257.0722.

Example 46. 2-((5-((4-fluoropiperidin-1-yl)methyl)thiophen-2-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 124

(394) 2-((5-((4-fluoropiperidin-1-yl)methyl)thiophen-2-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine was synthesized in 4 steps. Initially, the corresponding alkyne 125 was prepared in 3 steps from the compound 126 and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 46.1 Synthesis of 1-((5-ethynylthiophene-2-yl)methyl)-4-fluoropiperidine 125

(395) ##STR00329##

Synthesis of 1-((5-ethynylthiophene-2-yl)methyl)-4-fluoropiperidine 125

(396) ##STR00330##

(397) The compound was prepared according to procedure H and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=10/90). Brown oil (79%). Rf=0.45 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3287, 2949, 1358, 1035, 808, 576, 546, 525. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.09 (dd, J=1.3 Hz, 1H), 6.66-6.78 (m, 1H), 4.48-4.82 (m, 1H), 3.58-3.70 (m, 2H), 3.18-3.37 (m, 1H), 2.74 (m, 4H), 1.68-1.96 (m, 4H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 153.4 (Cq), 135.7 (Cq), 116.9 (Cq), 109.8 (Cq), 88.1 (d, J=170.6 Hz, CH), 81.8 (CH), 74.1 (Cq), 54.80 (CH.sub.2), 49.1 (d, J=5.7 Hz, 2CH.sub.2), 31.3 (d, J=19.7 Hz, 2CH.sub.2). F.sup.19 NMR (235 MHz, CDCl.sub.3, 20 C.) 181. HRMS (+ESI): calculated for C.sub.12H.sub.14FNS 223.31, found: 223.09.

Example 46.2 2-((5-((4-fluoropiperidin-1-yl)methyl)thiophen-2-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 124

(398) ##STR00331##

(399) The compound was synthesized according to procedure H and purified by flash column chromatography on silica gel (DCM/MeOH/NH.sub.4OH=94/4/2). Yellowish solid (60%). mp: 148 C. Rf=0.60 (DCM/MeOH/NH.sub.4OH=94/4/2). IR (v, cm.sup.1, neat) 1283, 1123, 1101, 986, 926, 806, 767, 622, 566, 526. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 10.86 (s, 1H), 8.50-8.31 (m, 1H), 7.95 (d, J=7.8 Hz, 1H), 7.23 (d, J=3.6 Hz, 1H), 7.14 (dd, J=7.8, 4.7 Hz, 1H), 6.87 (d, J=3.6 Hz, 1H), 6.78 (s, 1H), 4.88-4.51 (m, 1H), 3.74 (s, 2H), 2.59 (ddt, J=24.7, 11.0, 4.6 Hz, 4H), 1.94 (ddt, J=24.7, 11.0, 4.6 Hz, 4H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 148.4 (Cq), 145.5 (Cq), 144.1 (Cq), 132.41 (Cq), 129.1 (Cq), 125.7 (Cq), 121.5 (d, J=99.3 Hz, Cq), 120.5 (Cq), 119.5 (Cq), 116.5 (CH), 106.6 (CH), 87.16 (CH), 84.9 (CH), 57.3 (CH.sub.2), 49.2 (d, J=5.7 Hz, CH.sub.2), 49.2 (CH.sub.2), 31.5 (d, J=19.5 Hz, CH.sub.2), 31.3 (CH.sub.2). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) 135.79 (m, 1F). HRMS (+ESI) calculated for C.sub.19H.sub.18FN.sub.3S (M+H+): 340.1278, found: 340.1273.

Example 47. 2-((5-((4-fluoropiperidin-1-yl)methyl)furan-2-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 128

(400) 2-((5-((4-fluoropiperidin-1-yl)methyl)furan-2-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine was synthesized in 4 steps. Initially, the corresponding alkyne 130 was prepared in 3 steps from the compound 122 and then we did the Sonogashira reaction with azaindole to obtain the final compound.

Example 47.1 Synthesis of 1-((5-ethenylfuran-2-yl)methyl)-4-fluoropiperidine 130

(401) ##STR00332##

Synthesis of 1-((5-ethenylfuran-2-yl)methyl)-4fluoropiperidine 130

(402) ##STR00333##

(403) The compound was prepared according to procedure H and purified by flash column chromatography on silica gel (methanol/dichloromethane=2/98). Brown oil (79%). Rf=0.45 (methanol/dichloromethane=2/98). IR (v, cm.sup.1, neat) 3280, 1425, 1332, 1203, 1018, 795, 537, 520, 506. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 6.49 (d, 1H, J=3.3 Hz), 6.05-6.17 (m, 1H), 4.42-4.73 (m, 1H), 3.41-3.50 (m, 2H), 3.29-3.37 (m, 1H), 2.22-2.61 (m, 4H), 1.64-1.87 (m, 4H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 153.4 (Cq), 135.7 (Cq), 116.9 (Cq), 109.8 (Cq), 88.1 (d, J=170.6 Hz, CH), 81.8 (CH), 74.1 (Cq), 54.8 (CH.sub.2), 49.1 (d, J=5.7 Hz, 2CH.sub.2), 31.3 (d, J=19.7 Hz, 2CH.sub.2). HRMS (+ESI): calculated for C.sub.12H.sub.14FNO (M+H.sup.+): 208.11321, found: 208.11327.

Example 47.2 Synthesis of 2-((5-((4-fluoropiperidin-1-yl)methyl)furan-2-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 128

(404) ##STR00334##

(405) The compound was synthesized according to procedure C2 and purified by flash column chromatography on silicagel (methanol/dichloromethane/NH.sub.4OH=4/94/2). yellowish solid (77%). mp: 193 C. Rf=0.60 (methanol/dichloromethane/NH.sub.4OH=4/94/2). IR (v, cm.sup.1, neat) 3122, 3053, 2937, 2816, 1584, 1434, 1405, 1352, 1325, 1300, 1132, 1021, 975, 918, 820, 768. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 10.97 (s, 1H), 8.42 (s, 1H), 7.95 (d, J=7.9 Hz, 1H), 7.13 (dd, J=7.8, 4.5 Hz, 1H), 6.81 (s, 1H), 6.72 (d, J=3.4 Hz, 1H), 6.31 (d, J=3.3 Hz, 1H), 4.84-4.47 (m, 1H), 3.63 (s, 2H), 2.60 (ddt, J=59.6, 11.5, 5.6 Hz, 4H), 1.96 (ddt, J=24.6, 10.8, 4.7 Hz, 4H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 154.1 (Cq), 148.4 (Cq), 144.3 (CH), 136.0 (Cq), 129.2 (CH), 120.4 (Cq), 118.3 (Cq), 117.1 (CH), 116.6 (CH), 110.2 (CH), 107.1 (CH), 88.9 (d, J=170.6 Hz, CH), 85.72 (Cq), 83.7 (Cq), 54.9 (CH.sub.2), 49.1 (d, J=5.5 Hz, 2CH.sub.2), 31.3 (d, J=19.7 Hz, 2CH.sub.2). RMN .sup.19F (235 MHz, CDCl.sub.3, 20 C.) 136.58 (m, 1F). HRMS (+ESI) calculated for C.sub.19H.sub.18FN.sub.3O (M+H+): 340.1278, found: 340.1273.

Example 48. 1-(5-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)furan-2-yl)-N,N-dimethylmethanamine 131

(406) 1-(5-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)furan-2-yl)-N,N-dimethylmethanamine 131 was synthesized in 4 steps. Initially, the corresponding alkyne 132 was prepared in 3 steps from compound 122, followed by a Sonogashira reaction with azaindole for the final compound.

Example 48.1 Synthesis of ((5-ethenylfuran-2-yl)methyl)dimethylamine 132

(407) ##STR00335##

Synthesis of 1-(5-ethenylfuran-2-yl)-N,N-dimethylmethanamine 131

(408) The compound was prepared according to procedure H and purified by flash column chromatography on silicagel (methanol/dichloromethane=5/95). brown oil (79%). Rf=0.58 (methanol/dichloromethane=10/90). IR (v, cm.sup.1, neat): 3292, 2945, 2822, 2101, 1602, 1571, 1495, 1326, 1281, 1134, 1017, 992, 972, 936, 841, 792. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 6.55 (d, J=3.3 Hz, 1H), 6.16 (d, J=3.3 Hz, 1H), 3.50 (s, 2H), 3.35 (s, 1H, CH), 2.24 (d, J=4.4 Hz, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.): 6 153.9 (Cq), 135.8 (Cq), 117.1 (CH), 109.7 (CH), 81.9 (Cq), 74.2 (CH), 55.7 (CH.sub.2), 44.9 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.9H.sub.11NO (M+H.sup.+): 150.0913, found: 150.0915.

Example 48.2 1-(5-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)furan-2-yl)-N,N-dimethylmethanamine 131

(409) ##STR00336##

(410) The compound was synthesized according to procedure C2 and purified by flash column chromatography on silicagel (methanol/dichloromethane/NH.sub.4OH=4/94/2). yellowish solid (14%). Rf=0.43 (methanol/dichloromethane/NH.sub.4OH=4/94/2). mp: 144 C. IR (v, cm.sup.1, neat) 2980, 2761, 2202, 1585, 1403, 1358, 1296, 1258, 1223, 1144, 1022, 980, 845, 769, 513. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.45 (s, 1H), 8.30 (s, 1H), 7.87 (d, J=8.9 Hz, 1H), 7.02-6.79 (m, 2H), 6.45 (d, J=3.8 Hz, 1H), 3.48 (s, 2H), 2.17 (s, 6H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 155.9 (d, J=249.9 Hz, Cq), 155.8 (Cq), 145.7 (Cq), 134.9 (Cq), 133.7 (d, J=29.6 Hz, CH), 120.7 (Cq), 119.9 (d, J=7.5 Hz, Cq), 118.4 (CH), 114.44 (d, J=21.2 Hz, CH), 110.8 (CH), 107.4 (d, J=4.6 Hz, CH), 86.3 (Cq), 83.9 (Cq), 55.40 (CH.sub.2), 45.0 (2CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d6, 20 C.) . 138.2. HRMS (+ESI): calculated for C.sub.16H.sub.14FN.sub.3O (284.119367 g/mol), found (284.119244 g/mol).

Example 49. 1-(5-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)thiophen-2-yl)-N,N-dimethylmethanamine 133

(411) 1-(5-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)thiophen-2-yl)-N,N-dimethylmethanamine 133 was synthesized in 4 steps. Initially, the corresponding alkyne 134 was prepared in 3 steps from compound 126, followed by a Sonogashira reaction with azaindole to give the final compound.

Example 49.1 Synthesis of 1-(5-ethynylthiophene-2-yl)-N,N-dimethylmethanamine 134

(412) ##STR00337##

Synthesis of 1-(5-ethynylthiophene-2-yl)-N,N-dimethylmethanamine 134

(413) The compound was prepared according to procedure H and purified by flash column chromatography on silicagel (methanol/dichloromethane=5/95). Brown oil (74%) Rf=0.58 (methanol/dichloromethane=10/90). .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 6.68 (m, 1H), 6.55 (m, 1H), 3.60 (s, 2H) 3.26 (s, 1H), 2.14-2.24 (m, 6H). reaxys number: 10655856.

Example 49.2 1-(5-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)thiophen-2-yl)-N,N-dimethylmethanamine 133

(414) ##STR00338##

(415) The compound was synthesized according to procedure C2 and purified by flash column chromatography on silicagel (methanol/dichloromethane/NH.sub.4OH 4/94/2). yellowish solid (14.5%). mp: 162 C. Rf=0.72 (methanol/dichloromethane/NH.sub.4OH=4/94/2). IR (v, cm.sup.1, neat) 2980, 2761, 2202, 1585, 1503, 1403, 358, 1296, 1258, 1223, 1022, 980, 845, 769, 513. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 10.27 (d, J=6.4 Hz, 1H), 8.15-8.30 (m, 1H), 7.57 (dd, J=8.7, 2.8 Hz, 1H), 7.19 (d, J=3.7 Hz, 1H), 6.82 (d, J=3.8 Hz, 1H), 6.70 (d, J=2.1 Hz, 1H), 3.63 (s, 2H), 2.29 (d, J=3.4 Hz, 6H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 155.9 (d, J=249.9 Hz, Cq), 146.1 (Cq), 145.1 (Cq), 133.0 (Cq), 132.8 (CH), 125.9 (CH), 121.7-119.6 (m, 2Cq et CH), 114.2 (d, J=20.6 Hz, CH), 106.5 (d, J=4.5 Hz, CH), 87.8 (Cq), 84.4 (Cq), 58.5 (CH.sub.2), 45.1 (2CH.sub.3). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) 185.73. HRMS (+ESI) calculated for C.sub.16H.sub.14FN.sub.3S (M+H+): 300.09652, found: 300.09653.

Example 50. Procedure L: (Desylilation of Alkynes)

(416) The silylated alkyne (1.0 eq.) was reacted with K.sub.2CO.sub.3 (1.5 eq.) in methanol (0.03 M). After 3 h at room temperature, the solvent was evaporated under reduced pressure. The crude product is dissolved in 10 ml of ethyl acetate. Then, the organic phase was washed with brine (310 ml), the organic phase is dried with MgSO.sub.4 filtered through cotton and evaporated under reduced pressure. Finally, the crude product was purified by flash column chromatography on silicagel eluting with (ethyl acetate/petroleum ether) to yield the true alkyne.

Example 51. Procedure M: (Methylation)

(417) The alcohol derivative (1.0 eq.) is dissolved in THF. NaH (3.5 eq.) and CH.sub.3I (1.7 eq.) were added at 0 C. After 2 h at room temperature the mixture was cooled to 0 C. and a saturated solution of NH.sub.4Cl is added. The mixture was extracted with dichloromethane (310 ml). The organic phases are combined, dried over MgSO.sub.4, filtered through cotton and evaporated to dryness.

Example 52: 2-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-[1,1-biphenyl]-4-yl)(methyl)amino)ethan-1-ol 134

(418) ##STR00339##

(419) 2-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-[1,1-biphenyl]-4-yl)(methyl) amino)ethan-1-ol was synthesized in 5 steps. Initially, the corresponding alkyne was prepared in 3 steps and then engaged in a Sonogashira reaction with the azaindole. A deprotection reaction provides the final compound.

(420) ##STR00340##

Example 52.1 Synthesis of 4-bromo-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-methyl-[1,1-biphenyl]-4-amine 136

(421) Under argon, Pd(OAc).sub.2 (0.05 eq.) and Xantphos (0.067 mmol) were added to a degassed anhydrous toluene solution at a 0.3 M concentration containing the amine (3.0 eq.), brominated 119 (2.0 eq.) and Cs.sub.2CO.sub.3 (3.0 eq.). After 16 h at 100 C., the solvent was evaporated under reduced pressure and the reaction mixture was purified by flash column chromatography on silicagel to yield the brominated compound 136 as a white amorphous solid with a yield of 34%, Rf=0.20 (ethyl acetate/petroleum ether=1/99), IR (v, cm.sup.1, neat) 3284, 3070, 2929, 2856, 1610, 1513, 1495, 1471, 1427, 1360, 1280, 1234, 1160, 1103, 985, 927, 869. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.65 (d, J=7.2 Hz, 4H), 7.50 (d, J=8.5 Hz, 2H), 7.45-7.32 (m, 10H), 6.62 (d, J=8.5 Hz, 2H), 3.83 (t, J=6.2 Hz, 2H), 3.52 (t, J=6.2 Hz, 2H), 2.99 (s, 3H), 1.05 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 148.6 (Cq), 140.0 (Cq), 135.4 (4CH), 133.3 (2Cq), 131.5 (2CH), 129.5 (2CH), 127.5 (6CH), 127.3 (2CH), 127.0 (Cq), 119.6 (Cq), 111.9 (2CH), 60.9 (CH.sub.2), 54.3 (CH.sub.2), 39.0 (CH.sub.3), 26.7 (3CH.sub.3), 18.9 (Cq). HRMS (+ESI) calculated for C.sub.31H.sub.34BrNOSi (M+H.sup.+): 544.1665, found: 544.1663.

Example 52.2 Synthesis of N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-4-ethynyl-N-methyl-[1,1-biphenyl]-4-amine 135

(422) Alkyne 135 was prepared according to procedure II, at a temperature of 60 C. and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=2/48). Yellow oil (40% over two steps), Rf=0.20 (ethyl acetate/petroleum ether=2/48). IR (v, cm.sup.1, neat) 3277, 2928, 2855, 1609, 1599, 1532, 1493, 1471, 1426, 1371, 1357, 1292, 1240, 1210, 1194, 1134, 1104, 1087, 1006, 996, 982. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.65 (d, J=7.2 Hz, 4H), 7.50 (s1, 2H), 7.45-7.32 (m, 8H), 6.62 (d, J=8.5 Hz, 2H), 3.83 (t, J=6.2 Hz, 2H), 3.52 (t, J=6.2 Hz, 2H), 3.10 (s, 1H), 2.99 (s, 3H), 1.05 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 148.6 (Cq), 140.0 (Cq), 135.6 (4CH), 133.4 (2Cq), 132.5 (2CH), 129.7 (2CH), 127.7 (4CH), 127.6 (2CH), 127.4 (Cq), 125.8 (2CH), 119.6 (Cq), 112.0 (2CH), 84.0 (Cq), 77.1 (CH), 61.0 (CH.sub.2), 54.4 (CH.sub.2), 39.1 (CH.sub.3), 26.8 (3CH.sub.3), 19.1 (Cq). HRMS (+ESI) calculated for C.sub.33H.sub.35NOSi (M+H.sup.+): 490.2560, found: 490.2552.

Example 52.3 Preparation of 2-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-[1,1-biphenyl]-4-yl)(methyl)amino)ethan-1-ol 134

(423) The compound was prepared according to procedure C1 followed by procedure F and purified by flash column chromatography on silicagel (methanol/dichloromethane=2/48). yellowish solid (70% over 2 steps) mp 172-174 C., Rf=0.20 (methanol/dichloromethane=2/48). IR (u, cm.sup.1, neat) 3122, 2925, 1662, 1610, 1510, 1494, 1436, 1399, 1349, 1296, 1246, 1165, 1120, 1048, 984, 872, 839. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.38 (s, 1H), 8.28 (s, 1H), 7.86 (dd, J=2 et 9 Hz, 1H), 7.70 (m, 2H), 7.58 (m, 4H), 6.81 (m, 3H), 4.70 (t, J=7.3 Hz, 1H), 3.57 (m, 2H), 3.46 (d, J=7.3 Hz, 2H), 2.99 (s, 3H). .sup.13C NMR (101 MHz, DMSO-d.sub.6 20 C.) 155.3 (d, J=239.2 Hz, Cq), 147.9 (Cq), 145.6 (Cq), 144.9 (Cq), 133.2 (Cq), 132.8 (d, J=20.9 Hz, CH), 132.3 (2CH), 127.7 (2CH), 125.9 (2CH) 125.8 (Cq), 121.9 (Cq), 120.2 (d, J=6.2 Hz, Cq), 118.8 (Cq), 114.0 (d, J=20.2 Hz, CH), 112.5 (2CH), 106.6 (d, J=4.0 Hz, CH), 94.2 (Cq), 82.4 (Cq), 58.6 (CH.sub.2), 54.5 (CH.sub.2), 39.1 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 138.5.

Example 53: 4-((1H-pyrrolo[2,3-b]pyridine-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methyl-[1,1-biphenyl]-4-amine 137

(424) ##STR00341##

(425) 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methyl-[1,1-biphenyl]-4-amine 137 was synthesized in 7 steps. In a first step, corresponding alkyne was prepared in 3 steps and then engaged in a Sonogashira reaction with the azaindole and a deprotection reaction. Then, a fluorination reaction with DAST followed by a deprotection reaction of the azaindole leads to the expected compound

(426) ##STR00342##

Example 53.1 Preparation of tert-butyl 2-((4-((2-hydroxyethyl)(methyl)amino)-[1,1-biphenyl]-4-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 139

(427) The compound was prepared according to procedure C1 followed by procedure F and purified by flash column chromatography on silicagel (methanol/dichloromethane=2/48). Yellowish solid (48% over 2 steps) mp 200-202 C., Rf=0.20 (methanol/dichloromethane=2/48). IR (u, cm.sup.1, neat) 2979, 2204, 1742, 1605, 1573, 1544, 1517, 1355, 1306, 1253, 1189, 1154, 1115, 1089, 1041, 979, 813, 774, 527, 510. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.57 (m, 1H), 7.87 (d, J=7.3 Hz, 1H), 7.57 (m, 6H), 7.28 (s, 1H), 7.22 (m, 1H), 6.89 (m, 3H), 3.88 (m, 2H), 3.57 (t, J=5.7 Hz, 2H), 3.07 (s, 3H), 1.73 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 149.6 (Cq), 148.6 (Cq), 147.9 (Cq), 146.1 (CH), 141.4 (Cq), 131.9 (2CH), 128.6 (CH), 128.4 (Cq), 127.8 (2CH), 126.1 (2CH), 121.4 (Cq), 121.3 (Cq), 120.0 (Cq), 118.9 (CH), 113.0 (2CH), 112.5 (CH), 105.3 (Cq), 95.9 (Cq), 84.8 (Cq), 81.9 (Cq), 60.2 (CH.sub.2), 55.1 (CH.sub.2), 38.9 (CH.sub.3), 28.2 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.29H.sub.29N.sub.3O.sub.3 (M+H.sup.+): 468.2281, found: 468.2287.

Example 53.2 Preparation of 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methyl-[1,1-biphenyl]-4-amine 138

(428) To a solution containing compound 139 (0.035 g, 0.075 mmol, 1.0 eq.) in dichloromethane (5 ml), cooled to 78 C. is added dropwise DAST (0.012 ml, 0.089 mmol, 1.2 eq.). Then, the reaction medium is brought to 0 C. and after 50 minutes 1 ml of H.sub.2O is added. The aqueous phase is extracted with dichloromethane (2 times 10 ml), the combined organic phases are dried over MgSO.sub.4, filtered and concentrated under reduced pressure. The compound is purified by flash column chromatography on silicagel (methanol/dichloromethane=2/98). White solid (22%), mp >260 C., Rf=0.8 (methanol/dichloromethane=4/96). IR (v, cm.sup.1, neat) 2924, 1740, 1629, 1597, 1495, 1473, 156, 1400, 1359, 1337, 1301, 1250, 1209, 1153, 1140, 1108, 1086, 1043, 976, 906, 873. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.52 (dd, J=4.8, 1.6 Hz, 1H), 7.82 (dd, J=7.9, 1.6 Hz, 1H), 7.51 (d, J=8.8 Hz, 6H), 7.18 (dd, J=7.9, 4.8 Hz, 3H), 6.86 (s, 1H), 6.78 (d, J=8.8 Hz, 2H), 4.62 (dt, J=47.1, 5.2 Hz, 2H), 3.69 (dt, J=24.3, 5.2 Hz, 2H), 3.06 (s, 3H), 1.68 (s, H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 148.65 (Cq), 147.48 (Cq), 146.1 (CH), 131.9 (2CH), 128.6 (CH), 128.31 (Cq), 128.18 (Cq), 127.8 (2CH), 126.0 (2CH), 121.43 (Cq), 121.31 (Cq), 120.0 (Cq), 118.9 (CH), 112.6 (CH), 112.5 (2CH), 96.1 (Cq), 84.8 (Cq), 81.8 (d, J=170.3 Hz, CH.sub.2), 80.0 (Cq), 52.6 (d, J=21.2 Hz, CH.sub.2), 39.1 (CH.sub.3), 28.2 (3CH.sub.3). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) 222.2. HRMS (+ESI) calculated for C.sub.23H.sub.25FN.sub.3O.sub.2 (M+H+): 394.1925, found: 394.1925.

Example 53.3 Preparation of 4-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methyl-[1,1-biphenyl]-4-amine 137

(429) Compound 137 was prepared according to procedure F and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80). Yellow solid (29%), mp >260 C., Rf=0.28 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1-, neat) 2882, 2357, 1607, 1595, 1522, 1491, 1431, 1403, 1372, 1355, 1324, 1280, 1247, 1203, 1134, 1112, 1038, 977, 916. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.21 (s, 1H), 8.29 (s, 1H), 7.97 (d, J=7.9 Hz, 1H), 7.70 (d, J=8.0 Hz, 2H), 7.60 (d, J=8.0 Hz, 3H), 7.11 (dd, J=7.9, 4.7 Hz, 1H), 6.84 (m, 3H), 4.62 (d, J=47.7, 4.7 Hz, 2H), 3.72 (d, J=26.4, 4.7 Hz, 2H), 3.00 (s, 3H). .sup.13C NMR (101 MHz, DMSO-d.sub.6 20 C.) 149.3 (Cq), 148.8 (Cq), 144.8 (CH), 141.2 (Cq), 132.3 (2CH), 128.8 (CH), 127.7 (2CH), 126.6 (Cq), 126.0 (2CH), 125.9 (Cq), 120.0 (Cq), 119.6 (Cq), 119.2 (Cq), 116.8 (CH), 112.9 (2CH), 112.5 (Cq), 106.6 (CH), 93.57 (Cq), 82.9 (Cq), 82.8 (d, J=170.3 Hz, CH.sub.2), 52.1 (d, J=21.2 Hz, CH.sub.2), 38.94 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 221.2. HRMS (+ESI) calculated for C.sub.24H.sub.20FN.sub.3 (M+H+): 370.1714, found: 370.1707.

Example 54: 3-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 140

(430) ##STR00343##

(431) 3-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline was synthesized in 4 steps from dibromobenzene. initially, the corresponding alkyne 142 was prepared in 3 steps and the Sonogashira reaction with protected azaindole provides the intermediate 143. then, the alcohol function is liberated using the TBAF and finally compound 140 is obtained after three successive reactions (tosylation, nucleophilic substitution and deprotection).

(432) ##STR00344##

Example 54.1 Synthesis of 3-bromo-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-methylaniline 141

(433) Compound 141 was prepared according to procedure H and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=1/49). Colorless oil (43%). IR (v, cm.sup.1, neat) 3370, 2929, 2856, 1592, 1496, 1471, 1426, 1370, 1239, 1210, 1189, 1104, 926. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.60 (d, J=6.5 Hz, 4H), 7.50-7.26 (m, 6H), 6.95 (t, J=8.1 Hz, 1H), 6.73 (m, 2H), 6.44 (d, J=7.3 Hz, 1H), 3.76 (t, J=6.0 Hz, 2H), 3.43 (t, J=6.0 Hz, 2H), 2.88 (s, 3H), 1.01 (s, 9H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 150.4 (Cq), 135.6 (4CH), 133.3 (2Cq), 130.2 (CH), 129.7 (CH), 127.7 (5CH), 123.41 (Cq), 118.6 (CH), 114.2 (CH), 110.4 (CH), 61.1 (CH.sub.2), 54.4 (CH.sub.2), 39.0 (CH.sub.3), 26.79 (2CH.sub.3), 19.06 (Cq). HRMS (+ESI) calculated for C.sub.25H.sub.30BrNOSi (M+H+): 468.1352, found: 468.1356.

Example 54.2 Synthesis of N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-3-ethynyl-N-methylaniline 142

(434) Alkyne 142 was prepared according to procedure II and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=2/48). Colorless oil (86% over two steps). IR (v, cm.sup.1, neat) 3288, 2929, 2856, 1594, 1570, 1494, 1471, 1427, 1360, 1105, 1003, 822. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.62 (d, J=6.5 Hz, 4H), 7.50-7.26 (m, 6H), 7.08 (t, J=8.1 Hz, 1H), 6.78 (m, 2H), 6.54 (d, J=7.3 Hz, 1H), 3.79 (t, J=6.0 Hz, 2H), 3.47 (t, J=6.0 Hz, 2H), 2.97 (s, 1H), 2.90 (s, 3H), 1.01 (s, 9H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 150.4 (Cq), 135.6 (4CH), 133.4 (2Cq), 129.9 (CH), 129.0 (CH), 127.7 (5CH), 122.4 (Cq), 119.8 (CH), 115.2 (CH), 112.6 (CH), 84.9 (Cq) 75.8 (CH), 61.1 (CH.sub.2), 54.4 (CH.sub.2), 39.0 (CH.sub.3), 26.79 (2CH.sub.3), 19.06 (Cq). HRMS (+ESI) calculated for C.sub.25H.sub.30BrNOSi (M+H.sup.+): 468.1352, found: 468.1356.

Example 54.3 Preparation of tert-butyl 2-((3-((2-((tert-butyldiphenylsilyl)oxy)ethyl)(methyl)amino) phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 143

(435) Compound 137 was prepared according to procedure C2 and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80). Yellow oil (86%), Rf=0.20 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 2986, 2360, 2198, 1749, 1605, 1544, 1514, 1407, 1348, 1306, 1253, 1187, 1170, 1114, 1092, 1010, 972, 900, 804, 776, 663, 556, 508. .sup.1H NMR (400 MHz, CDC.sub.3, 20 C.) 8.57 (d, J=3.4 Hz, 1H), 7.86 (d, J=8.1 Hz, 1H), 7.66 (d, J=7.8 Hz, 4H), 7.39 (m, 6H), 7.19 (m, 2H), 6.87 (m, 3H), 6.62 (d, J=7.8 Hz, 1H), 3.84 (t, J=5.9 Hz, 2H), 3.54 (t, J=5.9 Hz, 2H), 2.99 (s, 3H), 1.67 (s, 9H), 1.06 (s, 9H). .sup.13C NMR (101 MHz, CDC.sub.3, 20 C.) 148.9 (Cq), 148.6 (Cq), 147.9 (Cq), 146.1 (CH), 135.6 (4CH), 133.4 (Cq), 129.7 (CH), 129.2 (CH), 128.6 (CH), 127.7 (5CH), 123.0 (Cq), 121.4 (Cq), 119.2 (CH), 118.9 (CH), 114.5 (CH), 112.7 (CH), 112.4 (CH), 96.8 (Cq), 84.7 (Cq), 80.4 (Cq), 61.2 (CH.sub.2), 54.4 (CH.sub.2), 39.1 (CH.sub.3), 28.2 (3CH.sub.3), 26.8 (3CH.sub.3), 19.1 (Cq). HRMS (+ESI) calculated for C.sub.39H.sub.43N.sub.3O.sub.3Si (M+H.sup.+): 630.3146, found: 630.3136.

Example 54.4 Preparation of tert-butyl 2-((3-((2-hydroxyethyl)(methyl)amino)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate 144

(436) Compound 144 was prepared according to procedure D and purified by flash column chromatography on silicagel (methanol/dichloromethane=4/96). Yellow oil (63%), Rf=0.20 (methanol/dichloromethane=4/96). IR (v, cm.sup.1, neat) 3386, 2980, 2926, 2206, 1747, 1603, 1546, 1517, 1473, 1408, 1384, 1343, 1305, 1249, 1194, 1154, 1117, 1085, 980, 847, 831, 814, 776, 746, 643, 525. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.54 (d, J=4.3 Hz, 1H), 7.82 (s, 1H), 7.25-7.16 (m, 2H), 6.99-6.77 (m, 4H), 3.84 (t, J=5.7 Hz, 2H), 3.50 (t, J=5.7 Hz, 2H), 3.00 (s, 3H), 1.69 (s, 9H). .sup.13C NMR (101 MHz, CDC.sub.3, 20 C.) 148.8 (Cq), 148.6 (Cq), 147.9 (Cq), 146.1 (CH), 129.3 (CH), 128.6 (CH), 121.4 (Cq), 121.2 (Cq), 120.2 (CH), 118.9 (CH), 115.4 (CH), 113.9 (CH), 112.9 (CH), 112.4 (CH), 96.4 (Cq), 84.7 (Cq), 80.7 (Cq), 60.1 (CH.sub.2), 55.2 (CH.sub.2), 38.9 (CH.sub.3), 28.2 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.23H.sub.25N.sub.3O.sub.3 (M+H.sup.+): 392.1968, found: 392.1967.

Example 54.5 Preparation of 3-((1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 140

(437) ##STR00345##

(438) At 0 C., TsCl (0.056 g, 0.294 mmol, 1.2 eq.), triethylamine (0.05 ml, 0.36 mmol, 1.5 eq.) and 4-DMAP (0.003 g, 0.024 mmol, 0, 1 eq.) were added to a solution of 144 (0.96 g, 0.245 mmol, 1.0 eq.) dissolved in DCM (5 ml). The mixture was stirred at room temperature overnight, then the mixture is neutralized with 10 ml of water and the aqueous phase is extracted with dichloromethane (2 times 10 ml). The combined organic phases were dried over MgSO.sub.4, filtered and concentrated under reduced pressure. The crude was purified by flash column chromatography on silicagel to afford 73 mg of tosylated compound with a yield of 55%. Then, the product is dissolved in 5 ml of THF and 0.94 ml of TBAF (C=1 M, 0.94 mmol, 7.0 eq.) was added dropwise. After 24 h at RT, 10 ml of H.sub.2O were added and the aqueous phase is extracted with dichloromethane (2 times 10 ml). The combined organic phases were dried over MgSO.sub.4, filtered and concentrated under reduced pressure. Finally, the crude is dissolved in dichloromethane (0.05 M) and at 0 C., TFA was added dropwise (ratio TFA/dichloromethane=1/2). Stirring at 0 C. is carried out with TLC monitoring. At the end of the reaction, the reaction mixture was evaporated under reduced pressure. The crude is taken up in DCM/NaOH (1M). With stirring, the aqueous phase is extracted with dichloromethane (2 times 10 ml). The combined organic phases were dried over MgSO.sub.4, filtered and concentrated under reduced pressure, prior to purifying the crude reaction product by flash column chromatography on silicagel (methanol/dichloromethane=4/96). Yellow solid (28%), Rf=0.15 (methanol/dichloromethane=4/96). IR (v, cm.sup.1, neat) 3386, 2980, 2926, 2206, 1747, 1603, 1546, 1517, 1473, 1408, 1384, 1343, 1305, 1249, 1194, 1154, 1117, 1085, 980, 847, 831, 814, 776, 746, 643, 525. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.13 (s, 1H), 8.23 (d, J=4.9 Hz, 1H), 7.91 (d, J=7.9 Hz, 1H), 7.20 (t, J=7.9 Hz, 1H), 7.14-7.02 (m, 1H), 6.89-6.70 (m, 4H), 4.56 (dt, J=47.6, 5.0 Hz, 2H), 3.65 (dt, J=26.4, 5.0 Hz, 2H), 2.93 (s, 3H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 148.8 (Cq), 148.6 (Cq), 147.9 (Cq), 144.8 (CH), 129.9 (CH), 128.8 (CH), 121.4 (Cq), 121.2 (Cq), 119.5 (CH), 116.8 (CH), 114.6 (CH), 113.7 (CH), 106.5 (CH), 94.5 (Cq), 82.9 (Cq), 82.8 (d, J=170.3 Hz, CH.sub.2), 52.1 (d, J=21.2 Hz, CH.sub.2), 38.6 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 221.03. HRMS (+ESI) calculated for C.sub.18H.sub.16FN.sub.3 (M+H.sup.+): 294.1401, found: 294.1401.

Example 55: 2-((3-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)(methyl) amino)ethan-1-ol 145

(439) ##STR00346##

(440) 2-((3-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)(methyl)amino)ethan-1-ol was synthesized in 2 steps from alkyne 142. Initially, a Sonogashira reaction is performed between the fluorinated azaindole and alkyne 142. Finally, a deprotection reaction using TBAF in is performed to yield the final compound

(441) ##STR00347##

(442) Compound 145 was prepared according to procedure C followed by procedure J and purified by flash column chromatography on silicagel (methanol/dichloromethane=4/96). Yellow solid (53%), Rf=0.10 (methanol/dichloromethane=2/98). mp=158-160 C. IR (v, cm.sup.1, neat) 2861, 2809, 1593, 1567, 1489, 1426, 1398, 1365, 1346, 1295, 1221, 1148, 1123, 1052, 1006, 987, 929, 892. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.35 (s, 1H), 8.27 (s, 1H), 7.85 (m, 1H), 7.27-7.18 (m, 1H), 6.83 (m, 4H), 4.70 (s, 1H), 3.61-3.52 (m, 2H), 3.46-3.38 (m, 2H), 2.96 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 154.5 (d, J=239.2 Hz, Cq), 149.6 (Cq), 145.6 (Cq), 132.7 (d, J=29.0 Hz, CH), 129.9 (CH), 122.3 (2Cq), 120.1 (d, J=7.2 Hz, Cq), 118.9 (CH), 114.8 (CH), 114.1 (d, J=20.8 Hz, CH), 113.9 (CH), 106.5 (d, J=4.0 Hz, CH), 95.0 (Cq), 81.0 (Cq), 58.5 (CH.sub.2), 54.5 (CH.sub.2), 39.4 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 138.5, HRMS (+ESI) calculated for C.sub.18H.sub.16FN.sub.3O (M+H+): 310.1350; found: 310.1349.

Example 56: N.SUP.1.-(4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)-N.SUP.1.,N.SUP.2.,N.SUB.2.-trimethylethane-1,2-diamine 147

(443) ##STR00348##

(444) N-(4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)-N.sup.1,N.sup.2,N.sup.2-trimethylethane-1,2-diamine 147 was synthesized in 4 steps. Initially, the alkyne 148 was prepared in 3 steps from dibromobenzene and Sonogashira reaction with azaindole provides the final compound.

(445) ##STR00349##

Example 56.1 Synthesis of N.SUP.1.-(4-bromophenyl)-N.SUP.1.,N.SUP.2.,N.SUP.2.-trimethylethane-1,2-diamine 149

(446) Compound 149 was prepared according to procedure H and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=1/49). Orange oil (61%). IR (v, cm.sup.1, neat) 3291, 2962, 2930, 2853, 2102, 1606, 1511, 1463, 1434, 1373, 1356, 1336, 1273, 1245, 1227, 1185, 1141, 1093, 1023, 935. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.25 (d, J=8.7 Hz, 2H), 6.54 (d, J=8.7 Hz, 2H), 3.39 (m, 2H), 2.89 (s, 3H), 2.53-2.35 (m, 2H), 2.25 (s, 6H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 148.1 (Cq), 131.8 (2CH), 113.7 (2CH), 108.0 (Cq), 55.8 (CH.sub.2), 51.2 (CH.sub.2), 45.9 (2CH.sub.3), 38.6 (CH.sub.3). HRMS (+ESI) calculated for C.sub.11H.sub.17BrN.sub.2 (M+H.sup.+): 257.0647, found: 257.0646.

Example 56.2 Synthesis of N.SUP.1.-(4-ethynylphenyl)-N.SUP.1.,N.SUP.2.,N.SUP.2.-trimethylethane-1,2-diamine 148

(447) Alkyne 148 was prepared according to procedure II and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=2/48). yellowish oil (35% over two steps). IR (v, cm.sup.1, neat) 2931, 2819, 2769, 2098, 1606, 1515, 1455, 133, 1324, 1300, 1250, 1215, 1175, 1113. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.37 (d, J=8.5 Hz, 2H), 6.63 (d, J=8.5 Hz, 2H), 3.39 (m, 2H), 2.90 (s, 4H), 2.55-2.41 (m, 2H), 2.31 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 149.1 (Cq), 133.4 (2CH), 111.4 (2CH), 108.6 (Cq), 84.8 (Cq), 74.7 (CH), 55.9 (CH.sub.2), 50.9 (CH.sub.2), 45.9 (2CH.sub.3), 38.5 (CH.sub.3).

Example 56.3 Synthesis of N-(4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)-N.SUP.1.,N.SUP.2.,N.SUP.2.-trimethylethanecm-1,2-diamine 147

(448) ##STR00350##

(449) The compound was prepared according to procedure C2 and purified by flash column chromatography on silicagel (methanol/dichloromethane/ammonia=4/96/1). yellow solid (80%), mp: 220-222 C., Rf=0.15 (methanol/dichloromethane=4/96). IR (v, cm.sup.1, neat) 2775, 2360, 2342, 1738, 1604, 1583, 1530, 1503, 1462, 1427, 1382, 1295, 1260, 1219, 1186, 1168, 1155, 1118, 1104, 1063, 1040, 1016, 981, 971, 957, 885. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.23 (s, 1H), 8.23 (m, 1H), 7.80 (dd, J=9.5, 2.5 Hz, 1H), 7.38 (d, J=8.6 Hz, 2H), 6.76-6.67 (m, 3H), 3.49 (t, J=7.1 Hz, 2H), 2.97 (s, 3H), 2.43 (t, J=7.1 Hz, 2H), 2.23 (s, 6H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 155.8 (d, J=239.4 Hz, Cq), 149.7 (Cq), 145.6 (Cq), 133.1 (2CH), 132.1 (d, J=27.4 Hz, CH), 122.9 (Cq), 120.3 (d, J=7.5 Hz, Cq), 113.7 (2CH), 112.0 (d, J=20.8 Hz, CH), 107.4 (Cq), 105.4 (d, J=4.0 Hz, CH), 95.5 (Cq), 80.1 (Cq), 55.4 (CH.sub.2), 49.9 (CH.sub.2), 45.9 (2CH.sub.3), 38.6 (CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 138.4. HRMS (+ESI) calculated for C.sub.20H.sub.21FN.sub.4 (M+H.sup.+): 337.1823, found: 337.1821.

Example 57: 8-(4-((5-fluoro-1H-pyrrolo[2,3-b] pyridin-2-yl)ethynyl)phenyl)-8-azaspiro[4.5]decane 150

(450) ##STR00351##

(451) 8-(4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)-8-azaspiro[4.5]decane 150 was synthesized in 3 steps. Initially, the corresponding alkyne 151 was prepared from brominated 152 then a Sonogashira reaction was performed on the azaindole to obtain the final compound

(452) ##STR00352##

Example 57.1 Synthesis of 8-(4-ethynylphenyl)-8-azaspiro[4.5]decane 151

(453) Compound 151 was prepared according to procedure H followed by procedure L and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=1/49). pale yellow amorphous solid (41% over 2 steps). IR (v, cm.sup.1, neat) 3302, 2915, 2849, 2096, 1729, 1678, 1602, 1554, 1508, 1463, 1448, 1389, 1345, 1309, 1248, 1193, 1137, 1067, 998, 951, 899, 858. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.38 (d, J=8.7 Hz, 2H), 6.85 (d, J=8.7 Hz, 2H), 3.29-3.20 (m, 4H), 2.99 (s, 1H), 1.72-1.58 (m, 8H), 1.49 (m, 4H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 151.6 (Cq), 133.2 (2CH), 114.9 (2CH), 110.9 (Cq), 84.5 (Cq), 75.1 (Cq), 46.3 (2CH.sub.2), 40.7 (Cq), 37.7 (2CH.sub.2), 37.0 (2CH.sub.2), 24.3 (2CH.sub.2). HRMS (+ESI) calculated for C.sub.17H.sub.21N (M+H.sup.+): 240.1745, found: 240.1746.

Example 57.2 Synthesis of 8-(4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)-8-azaspiro[4.5]decane 150

(454) ##STR00353##

(455) The compound was prepared according to procedure C2 and purified by silicagel column chromatography (methanol/dichloromethane=2/98). Yellow solid (40%), mp>260 C., Rf=0.22 (methanol/dichloromethane=2/98). IR (v, cm.sup.1, neat) 3119, 3058, 2921, 2827, 2200, 1601, 1585, 1533, 1504, 1462, 1385, 1344, 1287, 1243, 1226, 1186, 1155, 1138, 1107, 998, 984, 952, 898, 878. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.26 (s, 1H), 8.24 (s, 1H), 7.81 (m, 1H), 7.39 (d, J=8.9 Hz, 2H), 6.97 (d, J=8.9 Hz, 2H), 6.72 (s, 1H), 3.34-3.24 (m, 4H), 1.61 (s, 4H), 1.54-1.40 (m, 8H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 155.6 (d, J=239.4 Hz, Cq), 150.6 (Cq), 144.7 (Cq), 132.0 (2CH), 131.6 (d, J=27.4 Hz, CH), 121.8 (Cq), 119.4 (d, J=7.5 Hz, Cq), 114.1 (2CH), 112.8 (d, J=20.8 Hz, CH), 108.6 (Cq), 104.8 (d, J=4.0 Hz, CH), 94.2 (Cq), 79.4 (Cq), 44.63 (2CH.sub.2), 40.1 (Cq), 36.7 (2CH.sub.2), 35.9 (2CH.sub.2), 24.4 (2CH.sub.2). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 138.4. HRMS (+ESI) calculated C.sub.24H.sub.24FN.sub.3 (M+H.sup.+): 374.2027, found: 374.2027.

Example 58 4-(4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenoxy)-N,N-dimethylaniline 154

(456) ##STR00354##

(457) 4-(4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenoxy)-N,N-dimethylaniline 154 was synthesized in 5 steps. Initially, the alkyne 155 was prepared in 4 steps starting from the phenyl ether 99. The Sonogashira reaction was carried out with the fluorinated azaindole to yield the final compound

(458) ##STR00355##

Example 58.1 Synthesis of 4-(4-iodophenoxy)-N,N-dimethylaniline 156

(459) Under argon, Pd.sub.2dba.sub.3 (0.05 eq.) and tBu.sub.3P (0.075 mmol) were added to a degassed anhydrous toluene solution of 0.3M concentration containing the amine (1.0 eq.), the iodine 100 (1.0 eq.) and t-BuONa (1.2 eq.). After 24 h at room temperature, the solvent was evaporated under reduced pressure. Then, the reaction mixture was concentrated under reduced pressure before being purified by flash column chromatography on silica gel. Compound 156 is obtained as a colorless oil with a yield of 22%., Rf=0.20 (ethyl acetate/petroleum ether=1/49). IR (v, cm.sup.1, neat) 3044, 2844, 2793, 1578, 1508, 1475, 1439, 1395, 1344, 1276, 1223, 1163, 1125, 1056, 1001, 947. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.52 (d, J=8.9 Hz, 2H), 6.91 (d, J=8.9 Hz, 2H), 6.74-6.62 (m, 4H), 2.91 (s, 6H). .sup.13C NMR DEPT (63 MHz, CDCl.sub.3, 20 C.) 138.5 (2CH), 121.2 (2CH), 119.4 (2CH), 114.1 (2CH), 41.4 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.14H.sub.14INO (M+H.sup.+): 340.0192, found: 340.0191.

Example 58.2 Synthesis of 4-(4-ethynylphenoxy)-N,N-dimethylaniline 155

(460) The catalyst [Pd(PPh.sub.3).sub.2Cl.sub.2] (1.5 mg, 0.002 mmol, 0.03 eq.) was added to a degassed solution of iodine 156 (80 mg, 0.131 mmol, 1.0 eq), ethynyltrimethylsilane (0.016 ml, 0.1 mmol, 1.5 eq.), CuI (1 mg, 0.002 mmol, 0.03 eq.), in the Et.sub.3N at a concentration of 0.3 M. The mixture was stirred at 85 C. for 4 h under argon atmosphere. Then, the reaction mixture was concentrated under reduced pressure before being purified by flash column chromatography on silicagel with eluent (ethyl acetate/petroleum ether=20/80) to obtain 28 mg of the intermediate which reacted with K.sub.2CO.sub.3 (19 mg, 0.140 mmol, 1.5 eq.) in 4 ml of DCM/methanol (1/1). After 3 h stirring at room temperature, the solution is filtered through cotton. After evaporation to dryness, the crude is purified by flash column chromatography on silica gel with eluent (ethyl acetate/petroleum ether=4/96) to obtain the alkyne 155 as a colorless oil in quantitative yield over 2 steps. Rf=0.20 (ethyl acetate/petroleum ether=4/96). IR (v, cm.sup.1, neat) 3284, 3070, 2929, 2856, 1610, 1513, 1495, 1471, 1427, 1360, 1280, 1234, 1160, 1103, 985, 927, 869. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.40 (d, J=8.6 Hz, 2H), 6.96 (d, J=9.0 Hz, 2H), 6.85 (d, J=8.6 Hz, 2H), 6.74 (d, J=9.0 Hz, 2H), 3.00 (s, 1H), 2.94 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 159.8 (Cq), 148.0 (Cq), 146.3 (Cq), 133.6 (2CH), 121.3 (2CH), 116.7 (2CH), 115.3 (Cq), 113.8 (2CH), 83.5 (Cq), 77.3 (CH), 41.1 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.16H.sub.15NO (M+Na+): 280.1308, found: 280.1312.

Example 58.3 Synthesis of 4-(4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenoxy)-N,N-dimethylaniline 154

(461) ##STR00356##

(462) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (methanol/dichloromethane=2/98). Yellow solid (31%), mp: 228-230 C., Rf=0.22 (methanol/dichloromethane=2/98). IR (v, cm.sup.1, neat) 3119, 3060, 2970, 2850, 2799, 1586, 1515, 1504, 1493, 1455, 1443, 1427, 1396, 1347, 1293, 1277, 1250, 1222, 1162, 1126, 1102, 1060, 985, 946, 893. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.30 (s, 1H), 8.22 (s, 1H), 7.79 (m, 1H), 7.50 (d, J=8.4 Hz, 2H), 6.92 (2d, J=8.4 Hz, 4H), 6.75 (d, J=7.7 Hz, 3H), 2.86 (s, 6H). .sup.13C NMR DEPT (63 MHz, DMSO-d.sub.6, 20 C.) 133.7 (2CH), 132.9 (d, J=27.4 Hz, CH), 121.7 (2CH), 117.1 (2CH), 114.2 (2CH), 113.8 (d, J=20.8 Hz, CH), 106.4 (d, J=4.0 Hz, CH), 41.00 (2CH.sub.3). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) . 138.5. HRMS (+ESI) calculated for C.sub.23H.sub.18FN.sub.3O (M+H.sup.+): 372.1506, found: 372.1505.

Example 59: 5-fluoro-2-((4-(4-(methylsulfonyl)piperazin-1-yl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 157

(463) ##STR00357##

(464) 5-fluoro-2-((4-(4-(methylsulfonyl)piperazin-1-yl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 157 was synthesized in 3 steps. Initially, the alkyne 158 was prepared in 2 steps from the bromine 152 then the Sonogashira reaction with azaindole allowed to obtain the final compound.

(465) ##STR00358##

Example 59.1 Synthesis of 1-(4-ethynylphenyl)-4-(methylsulfonyl)piperazine 158

(466) The compound 158 was prepared according to procedure H followed by Procedure L and purified by flash column chromatography on silica gel (ethyl acetate petroleum ether=30/70). White solid (14% over 2 steps), mp. 208-210 C., Rf=0.5 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 3245, 2928, 2836, 1605, 1508, 1448, 1389, 1374, 1340, 1329, 1319, 1286, 1263, 1237, 1204, 1179, 1156, 1139, 1114, 1065, 1049, 948, 908. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.39 (d, J=8.7 Hz, 2H), 6.82 (d, J=8.7 Hz, 2H), 3.34 (s1, 8H), 2.98 (s, 1H), 2.80 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 150.5 (Cq), 133.3 (2CH), 115.9 (2CH), 113.5 (Cq), 83.8 (Cq), 75.9 (Cq), 48.5 (2CH.sub.2), 45.6 (2CH.sub.2), 34.5 (CH.sub.3). HRMS (+ESI) calculated for C.sub.13H.sub.16N.sub.2O.sub.2S (M+H.sup.+): 265.1006, found: 265.1005.

Example 59.2 Synthesis of 5-fluoro-2-((4-(4-(methylsulfonyl)piperazin-1-yl)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 157

(467) ##STR00359##

(468) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=30/70). Yellow solid (33%), mp>260 C., Rf=0.33 (ethyl acetate/petroleum ether=30/70). IR (v, cm.sup.1, neat) 2971, 2901, 2361, 1729, 1606, 1559, 1541, 1507, 1448, 1393, 1373, 1323, 1291, 1259, 1223, 1186, 1174, 1132, 115, 1088, 1066, 1012, 937, 833, 817, 803. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.28 (s, 1H), 8.25 (s, 1H), 7.83 (d, J=9.1 Hz, 1H), 7.45 (d, J=8.5 Hz, 2H), 7.04 (d, J=8.7 Hz, 2H), 6.75 (s, 1H), 3.38 (d, J=5.0 Hz, 4H), 3.25 (d, J=5.0 Hz, 4H), 2.93 (s, 3H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 155.6 (d, J=239.4 Hz, Cq), 150.9 (Cq), 145.6 (Cq), 133.0 (2CH), 132.6 (d, J=27.4 Hz, CH), 122.5 (Cq), 120.3 (d, J=7.5 Hz, Cq), 115.7 (2CH), 113.9 (d, J=20.8 Hz, CH), 111.3 (Cq), 105.9 (d, J=4.0 Hz, CH), 94.7 (Cq), 80.7 (Cq), 47.4 (2CH.sub.2), 45.6 (2CH.sub.2), 34.4 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 138.6. HRMS (+ESI) calculated for C.sub.20H.sub.19FN.sub.4O.sub.2S (M+H.sup.+): 399.1285, found: 399.1285.

Example 60: 2-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)(methyl) amino)ethan-1-ol 160

(469) ##STR00360##

(470) 2-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)(methyl)amino)ethan-1-ol 160 was synthesized in 4 steps. Initially, the alkyne 161 was prepared in 2 steps from the bromine 152 then the Sonogashira reaction with azaindole followed by deprotection allows to obtain the final compound.

(471) ##STR00361##

Example 60.1 Synthesis of N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-4-ethynyl-N-methylaniline 161

(472) Compound 161 was prepared according to procedure H followed by procedure L and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=10/90). Yellow oil (44% over 2 steps). Rf=0.4 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3291, 2962, 2930, 2853, 2102, 1606, 1511, 1463, 1434, 1373, 1356, 1336, 1273, 1245, 1227, 1185, 1141, 1093, 1023, 935.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.68 (d, J=6.8 Hz, 3H), 7.40 (td, J=12.3, 11.8, 6.0 Hz, 7H), 6.49 (d, J=8.8 Hz, 2H), 3.83 (t, J=6.2 Hz, 2H), 3.52 (d, J=6.1 Hz, 2H), 2.98 (d, J=5.3 Hz, 3H), 1.09 (s, 9H).

Example 60.2 Synthesis of N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-methylaniline 163

(473) ##STR00362##

(474) Compound 163 was prepared according to procedure C2 and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=10/90). Yellow solid (78%), Rf=0.10 (ethyl acetate/petroleum ether=10/90). mp=182-184 C. IR (v, cm.sup.1, neat) 2922, 2852, 2198, 2008, 1605, 1584, 1537, 1504, 1470, 1426, 1377, 1349, 1294, 1233, 1188, 1154, 1107, 1007, 976, 871. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.23 (s, 1H), 7.66 (d, J=7.5 Hz, 4H), 7.59 (d, J=8.5 Hz, 1H), 7.46 (t, J=7.5 Hz, 2H), 7.39 (t, J=7.5 Hz, 6H), 6.68 (s, 1H), 6.55 (d, J=8.5 Hz, 2H), 3.84 (t, J=6.2 Hz, 2H), 3.54 (t, J=6.2 Hz, 2H), 3.01 (s, 3H), 1.07 (s, 9H). .sup.13C NMR DEPT (101 MHz, CDCl.sub.3, 20 C.) 133.0 (4CH), 132.8 (2CH), 132.3 (d, J=27.4 Hz, CH), 129.8 (2CH), 127.8 (4CH), 113.6 (d, J=20.8 Hz, CH), 111.5 (2CH), 106.4 (d, J=4.0 Hz, CH), 60.7 (CH.sub.2), 54.2 (CH.sub.2), 39.2 (CH.sub.3), 26.8 (3CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 138.54, HRMS (+ESI) calculated for C.sub.34H.sub.34FN.sub.3OSi (M+H.sup.+): 548.2527; found: 548.2528.

Example 60.3 Synthesis of 2-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)(methyl) amino)ethan-1-ol 160

(475) ##STR00363##

(476) Compound 160 was prepared according to procedure E and purified by flash column chromatography on silica gel (methanol/dichloromethane=4/96). Yellow solid (45%), Rf=0.10 (methanol/dichloromethane=2/98). mp=192-194 C. IR (v, cm.sup.1, neat) 3126, 2921, 2852, 2198, 1729, 1603, 1585, 1540, 1507, 1449, 1432, 1372, 1321, 1287, 1260, 1241, 1219, 1185, 1153, 1120, 1100, 1078, 1052, 978, 930, 917, 889, 892, 832. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.22 (s, 1H), 8.22 (s, 1H), 7.80 (m, 1H), 7.37 (d, J=8.5 Hz, 2H), 6.80-6.60 (m, 3H), 4.71 (s, 1H), 3.56 (m, 2H), 3.50-3.39 (m, 2H), 2.99 (s, 3H). .sup.13C NMR (101 MHz, DMSO-d6, 20 C.) 155.6 (d, J=239.4 Hz, Cq), 150.0 (Cq), 145.6 (Cq), 133.0 (2CH), 132.6 (d, J=27.4 Hz, CH), 123.3 (Cq), 120.3 (d, J=7.5 Hz, Cq), 113.4 (d, J=20.8 Hz, CH), 112.0 (2CH), 107.2 (Cq), 106.3 (d, J=4.0 Hz, CH), 95.6 (Cq), 80.6 (Cq), 58.5 (CH.sub.2), 54.3 (CH.sub.2), 39.2 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 138.4, HRMS (+ESI) calculated for C.sub.18H.sub.16FN.sub.3O (M+H.sup.+): 310.1350; found: 310.1349.

Example 61: 3-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)(methyl) amino)propan-1-ol 164

(477) ##STR00364##

(478) 3-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)(methyl)amino)propan-1-ol 164 was synthesized in 4 steps. Initially, the alkyne 165 was prepared in 3 steps from the bromine 152 then the Sonogashira reaction with azaindole followed by deprotection provides the final compound

(479) ##STR00365##

Example 61.1 Synthesis of 4-bromo-N-(3-((tert-butyldiphenylsilyl)oxy)propyl)-N-methylaniline 166

(480) Compound 166 was prepared according to procedure H and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=2/48). Orange oil (64%). Rf=0.55 (ethyl acetate/petroleum ether=2/48). IR (v, cm.sup.1, neat) 33070, 2929, 2856, 1592, 1496, 1471, 1426, 1370, 1239, 1210, 1189, 1104, 926. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.69 (d, J=7.2 Hz, 4H), 7.42 (m, 6H), 7.29 (m, 2H), 6.62 (d, J=8.5 Hz, 2H), 3.73 (t, J=7.3 Hz, 2H), 3.49 (t, J=7.3 Hz, 2H), 2.91 (s, 3H), 1.79 (p, J=6.5 Hz, 2H), 1.11 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 148.3 (Cq), 135.6 (4CH), 133.7 (2Cq), 131.7 (2CH), 129.7 (2CH), 127.7 (4CH), 113.8 (2CH), 107.7 (Cq) 1.3 (CH.sub.2), 49.4 (CH.sub.2), 38.3 (CH.sub.3), 29.4 (CH.sub.2), 26.9 (3CH.sub.3), 19.2 (Cq). HRMS (+ESI) calculated for C.sub.26H.sub.32BrNOSi (M+): 482.1509, found: 482.1509.

Example 61.2 Synthesis of N-(3-((tert-butyldiphenylsilyl)oxy)propyl)-4-ethynyl-N-methylaniline 165

(481) The alkyne 165 was prepared according to procedure 11 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=2/48). Yellowish oil (35% over two steps). Rf=0.50 (ethyl acetate/petroleum ether=2/48). IR (v, cm.sup.1, neat) 3288, 2929, 2856, 1594, 1570, 1494, 1471, 1427, 1360, 1105, 1003, 822. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.70-7.60 (m, 4H), 7.48-7.30 (m, 8H), 6.63 (d, J=8.9 Hz, 2H), 3.70 (t, J=5.7 Hz, 2H), 3.58-3.47 (m, 2H), 2.97 (s, 1H), 2.93 (s, 3H), 1.78 (s, 2H), 1.08 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 13C NMR (63 MHz, CDCl3) 149.3 (Cq), 135.6 (4CH), 133.7 (2Cq), 133.3 (2CH), 129.7 (2CH), 127.7 (4CH), 111.4 (CH), 108.2 (Cq) 84.9 (Cq), 74.6 (CH), 61.2 (CH.sub.2) 49.1 (CH.sub.2), 38.2 (CH.sub.3), 29.6 (CH.sub.2), 26.9 (3CH.sub.3), 19.2 (Cq). HRMS (+ESI) calculated for C.sub.28H.sub.33N.sub.2OSi (M+H.sup.+): 428.2404, found: 428.2399.

Example 61.3 Synthesis of 3-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2 yl)ethynyl)phenyl)(methyl) amino)propan-1-ol 164

(482) ##STR00366##

(483) The compound 164 was prepared according to procedure C2 followed by procedure E and purified by flash column chromatography on silica gel (methanol/dichloromethane=4/96). Yellow solid (48% over 2 steps), Rf=0.10 (methanol/dichloromethane=2/98). mp=192-194 C. IR (v, .sup.1, neat) 3126, 2921, 2852, 2198, 1729, 1603, 1585, 1540, 1507, 1449, 1432, 1372, 1321, 1287, 1260, 1241, 1219, 1185, 1153, 1120, 1100, 1078, 1052, 978, 930, 917, 889, 892, 832. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.23 (s, 1H), 8.22 (s, 1H), 7.80 (d, J=9.5 Hz, 1H), 7.37 (d, J=8.5 Hz, 2H), 6.77-6.67 (m, 3H), 4.58-4.51 (m, 1H), 3.51-3.39 (m, 4H), 2.95 (s, 3H), 1.68 (p, J=6.5 Hz, 2H). .sup.13C NMR (101 MHz, DMSO-d6, 20 C.) 155.6 (d, J=239.4 Hz, Cq), 150.0 (Cq), 145.6 (Cq), 133.0 (2CH), 132.6 (d, J=27.4 Hz, CH), 123.3 (Cq), 120.3 (d, J=7.5 Hz, Cq), 113.4 (d, J=20.8 Hz, CH), 112.0 (2CH), 107.2 (Cq), 106.3 (d, J=4.0 Hz, CH), 95.7 (Cq), 80.0 (Cq), 58.7 (CH.sub.2), 48.9 (CH.sub.2), 39.2 (CH.sub.3), 29.9 (CH.sub.2). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 138.54. HRMS (+ESI) calculated for C.sub.19H.sub.18FN.sub.3O (M+H.sup.+): 324.1505; found: 324.1504.

Example 62: (1-(2-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)(methyl)amino)ethyl)-1H-1,2,3-triazol-4-yl)methanol 167

(484) ##STR00367##

(485) (1-(2-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)(methyl)amino)ethyl)-1H-1,2,3-triazol-4-yl)methanol 167 was synthesized in 10 steps. Initially, the corresponding alkyne 168 was prepared in 8 steps from 1,4-dibromobenzene and then the Sonogashira reaction with azaindole followed by a deprotection reaction allowed to obtain the final compound.

(486) ##STR00368## ##STR00369##

Example 62.1 Synthesis of 4-bromo-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-methylaniline 169

(487) Compound 169 was prepared according to procedure H and purified by column flash chromatography on silica gel (ethyl acetate/petroleum ether=5/45). Orange oil (67%). Rf=0.65 (ethyl acetate/petroleum ether=1/49). IR (v, cm.sup.1, neat) 2929, 2855, 1588, 1496, 1471, 1427, 1356, 1314, 1253, 1218, 1190, 1141, 1105, 1079, 1045, 997, 936. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.69 (d, J=7.2 Hz, 4H), 7.42 (m, 6H), 7.29 (m, 2H), 6.62 (d, J=8.5 Hz, 2H), 3.73 (t, J=7.3 Hz, 2H), 3.49 (t, J=7.3 Hz, 2H), 2.91 (s, 3H), 1.11 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 148.3 (Cq), 135.6 (4CH), 133.7 (2Cq), 131.7 (2CH), 129.7 (2CH), 127.7 (4CH), 113.8 (2CH), 107.7 (Cq) 0.8 (CH.sub.2), 54.5 (CH.sub.2), 38.3 (CH.sub.3), 26.9 (3CH.sub.3), 19.2 (Cq). HRMS (+ESI) calculated for C.sub.25H.sub.30BrNOSi (M+): 468.1352, found: 468.1353.

Example 62.2 Synthesis of 2-((4-bromophenyl)(methyl)amino)ethan-1-ol 170

(488) Compound 170 was prepared according to procedure E and purified by flash column chromatography on silica gel (methanol/dichloromethane=4/96). Colorless oil (91%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.30 (d, J=8.3 Hz, 2H), 6.75-6.53 (d, J=8.3 Hz, 2H), 3.80 (m, 2H), 3.45 (m, 2H), 2.94 (s, 3H). CAS Number: 252949-11-4.

Example 62.3 Synthesis of 4-bromo-N-(2-iodoethyl)-N-methylaniline 171

(489) Under argon, 400 mg of 2-((4-bromophenyl) (methyl) amino)ethan-1-ol 170 (1.74 mmol, 1 0.0 eq) were dissolved in 18 ml of THF. At 0 C., 190 mg of imidazole (2.80 mmol, 1.6 eq.), 616 mg of triphenylphosphine (2.35 mmol, 1.35 eq.) and 574 mg of iodine (2.26 mmol, 1.3 eq.) were added. After 5 minutes at 0 C., the reaction mixture is brought to room temperature. I After 6 h stirring, 30 ml of saturated thiosulfate solution is added. The organic phase was extracted with ethyl acetate (330 ml). The organic phases are combined and washed with a saturated NaCl solution and then dried over MgSO.sub.4 filtered through cotton and evaporated to dryness. The crude was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=2/98) to obtain compound 171 (497 mg, 84%) as a colorless oil. Rf=0.9 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 2873, 2820, 1588, 1492, 1427, 1369, 1339, 1311, 1289, 1269, 1216, 1169, 1109, 1089, 971. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.31 (d, J=9.0 Hz, 2H), 6.56 (d, J=9.0 Hz, 2H), 3.73-3.65 (m, 2H), 3.23-3.17 (m, 2H), 2.96 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 146.9 (Cq), 132.1 (2CH), 113.7 (2CH), 109.0 (Cq), 55.5 (CH.sub.2), 38.4 (CH.sub.3), 1.8 (CH.sub.2). HRMS (+ESI) calculated for C.sub.9H.sub.11IBrN (M+H.sup.+): 341.9172, found: 341.9170.

Example 62.4 Synthesis of N-(2-azidoethyl)-4-bromo-N-methylaniline 172

(490) Under argon, 460 mg of 4-bromo-N-(2-iodoethyl)-N-methyl aniline 171 (1.35 mmol, 1.0 eq.) are dissolved in 5 ml of DMF. Then, 102 mg of azide (1.62 mmol, 1.2 eq.) were added. After 16 h stirring at room temperature, 30 ml of H.sub.2O are added. The organic phase was extracted with ethyl acetate (330 ml). The organic phases are combined and washed with a saturated NaCl solution and then dried over MgSO.sub.4, filtered through cotton and evaporated to dryness. The crude was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=4/96) to afford compound 171 (280 mg, 81%) as a colorless oil. Rf=0.85 (ethyl acetate/petroleum ether=10/90). IR (v, cm.sup.1, neat) 3292, 2940, 2870, 1594, 1570, 1494, 1480, 1435, 1370, 1155, 1003, 822. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.34 (d, J=9.0 Hz, 2H), 6.62 (d, J=9.0 Hz, 2H), 3.54 (t, J=5.8 Hz, 2H), 3.47 (t, J=5.8 Hz, 2H), 3.00 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 147.6 (Cq), 132.0 (2CH), 113.9 (2CH), 109.0 (Cq), 55.5 (CH.sub.2), 48.7 (CH.sub.2), 38.9 (CH.sub.3). HRMS (+ESI) calculated for C.sub.9H.sub.11BrN.sub.4 (M): 255.0239, found: 255.0238.

Example 62.5 Synthesis of (1-(2-((4-bromophenyl)(methyl)amino)ethyl)-1H-1,2,3-triazol-4-yl)methanol 173

(491) Under argon, 240 mg of N-(2-azidoethyl)-4-bromo-N-methylaniline 170 (0.94 mmol, 1.0 eq.) are dissolved in 1 ml of t-butanol/water (2/1). At room temperature, 0.055 ml of propargyl alcohol (0.94, 1.0 eq.), 25 mg of CuSO.sub.4, 5H.sub.2O (0.094 mmol, 0.1 eq.) and 19 mg of sodium ascorbate (0.094 mmol, 0.1 eq.) were added. After 16 h of stirring, 30 ml of water are added. The organic phase is extracted with dichloromethane (330 ml). The organic phases are combined and washed with a saturated NaCl solution and then dried over MgSO.sub.4, filtered through cotton and evaporated to dryness. The crude was purified by flash column chromatography on silica gel (methanol/dichloromethane=4/96) to afford compound 173 (260 mg, 89%) as a colorless oil. Rf=0 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 3297, 2873, 1588, 1494, 1449, 1430, 1355, 1314, 1255, 1215, 1191, 1141, 1113, 1079, 1038, 1009, 959. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.33 (m, 3H), 6.48 (d, J=9.0 Hz, 2H), 6.5 (s, 2H), 3.73-3.65 (m, 2H), 3.23-3.17 (m, 2H), 2.76 (s, 3H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 147.9 (Cq), 147.1 (Cq), 132.1 (2CH), 122.6 (CH), 113.7 (2CH), 109.0 (Cq), 56.5 (CH.sub.2), 53.0 (CH.sub.2), 47.5 (CH.sub.2), 38.8 (CH.sub.3).

Example 62.6 Synthesis of 4-bromo-N-(2-(4-(((tert-butyldiphenylsilyl)oxy)methyl)-1H-1,2,3-triazol-1-yl)ethyl)-N-methylaniline 174

(492) Under argon, the (1-(2-((4-bromophenyl) (methyl)amino)ethyl)-1H-1,2,3-triazol-4-yl)methanol 173 (735 mg, 2.35 mmol, 1.0 eq.) is dissolved in 50 ml of DCM. At 0 C., 0.7 ml of TBDPSCl (2.82 mmol, 1.2 eq.)), and 192 mg of imidazole (2.80 mmol, 1.2 eq.) were added. After 5 minutes at 0 C., the reaction mixture is brought to room temperature. After 16 h of stirring, 30 ml of water is added. The organic phase is extracted with dichloromethane (330 ml). The organic phases are combined and washed with a saturated NaCl solution and then dried over MgSO.sub.4, filtered through cotton and evaporated to dryness. The crude was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=20/80) to obtain compound 174 (1.2 g, 90%) as a colorless oil. Rf=0.25 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 2929, 2855, 1588, 1496, 1471, 1427, 1356, 1314, 1253, 1218, 1190, 1141, 1105, 1079, 1045, 997, 936. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.65 (d, J=6.5 Hz, 4H), 7.48-7.27 (m, 8H), 7.19 (s, 1H), 6.49 (d, J=9.0 Hz, 2H), 4.85 (s, 2H), 4.51 (t, J=6.1 Hz, 2H), 3.81 (t, J=6.1 Hz, 2H), 2.73 (s, 3H), 1.05 (s, 9H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 148.4 (Cq), 147.0 (Cq), 135.5 (4CH), 133.2 (2Cq), 132.1 (2CH), 129.8 (2CH), 127.8 (4CH), 122.6 (CH), 113.8 (2CH), 109.4 (Cq), 58.53 (CH.sub.2), 53.0 (CH.sub.2), 47.3 (CH.sub.2), 38.8 (CH.sub.3), 26.8 (3CH.sub.3), 19.2 (Cq). HRMS (+ESI) calculated for C.sub.28H.sub.33BrN.sub.4OSi (M+H.sup.+): 551.1660, found: 551.1664.

Example 62.7 Synthesis of N-(2-(4-(((tert-butyldiphenylsilyl)oxy)methyl)-1H-1,2,3-triazol-1-yl)ethyl)-4-ethynyl-N-methylaniline 168

(493) The alkyne 168 was prepared according to procedure 12 and purified by flash chromatographie column on silica gel (ethyl acetate/petroleum ether=30/70). Brown oil (38% over two steps). Rf=0.55 (ethyl acetate/petroleum ether=40/60). IR (v, cm.sup.1, neat) 3280, 2928, 2930, 2855, 2098, 1606, 1514, 1459, 1426, 1375, 1355, 1273, 1256, 1220, 1174, 1141. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.65 (d, J=6.5 Hz, 4H), 7.48-7.27 (m, 8H), 7.18 (s, 1H), 6.55 (d, J=9.0 Hz, 2H), 4.85 (s, 2H), 4.50 (t, J=6.1 Hz, 2H), 3.86 (t, J=6.1 Hz, 2H), 2.76 (s, 1H), 2.76 (s, 3H), 1.05 (s, 9H). .sup.13C NMR DEPT (63 MHz, CDCl.sub.3, 20 C.) 135.5 (4CH), 133.6 (2CH), 129.8 (2CH), 127.8 (4CH), 122.6 (CH), 111.6 (2CH), 75.3 (CH), 58.5 (CH.sub.2), 52.7 (CH.sub.2), 47.3 (CH.sub.2), 38.8 (CH.sub.3), 26.8 (3CH.sub.3), 19.2 (Cq). HRMS (+ESI) calculated for C.sub.30H.sub.34N.sub.40S (M+H.sup.+): 495.2573, found: 495.2575.

Example 62.8 Synthesis of (1-(2-((4-((5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)phenyl)(methyl) amino)ethyl)-1H-1,2,3-triazol-4-yl)methanol 167

(494) ##STR00370##

(495) Compound 167 was prepared according to procedure C2 followed by procedure E and purified by flash column chromatography on silica gel (methanol/dichloromethane=4/96). Yellow solid (74% over 2 steps), Rf=0.30 (methanol/dichloromethane=4/96). mp=222-224 C. IR (v, cm.sup.1, neat) 3311, 3121, 2901, 2202, 1605, 1585, 1540, 1508, 1475, 1448, 1431, 1378, 1357, 1323, 1291, 1257, 1231, 1185, 1156, 1109, 1073, 1052, 1036, 1012, 983, 965, 937, 869. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.22 (s, 1H), 8.22 (s, 1H), 7.99 (s, 1H), 7.80 (dd, J=8.8, 2.8 Hz, 1H), 7.37 (d, J=8.8 Hz, 2H), 6.72 (m, 3H), 5.14 (t, J=5.6 Hz, 1H), 4.52 (m, 4H), 3.85 (t, J=6.2 Hz, 2H), 2.79 (s, 3H). .sup.13C NMR (63 MHz, DMSO-d6, 20 C.) 155.6 (d, J=239.4 Hz, Cq), 149.3 (Cq), 148.6 (Cq), 145.63 (Cq), 133.0 (2CH), 132.6 (d, J=27.4 Hz, CH), 123.6 (CH), 122.9 (Cq), 120.4 (d, J=7.5 Hz, Cq), 113.7 (d, J=20.8 Hz, CH), 112.2 (2CH), 108.7 (Cq), 105.9 (d, J=4.0 Hz, CH), 95.3 (Cq), 80.0 (Cq), 55.5 (CH.sub.2), 52.01 (CH.sub.2), 47.1 (CH.sub.2), 39.2 (CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 138.54. HRMS (+ESI) calculated for C.sub.21H.sub.19FN.sub.6O (M+H.sup.+): 391.1675, found: 391.1677.

Example 63: 4-((3-((dimethylamino)methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 175

(496) ##STR00371##

(497) 4-((3-((dimethylamino)methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 175 was synthesized in 2 steps. Initially, the azaindole 176 is obtained by the Mannich reaction followed by the Sonogoshira reaction to obtain the desired final compound

(498) ##STR00372##

Example 63.1 Synthesis of 1-(2-iodo-1H-pyrrolo[2,3-b]pyridin-3-yl)-N,N-dimethylmethanamine 176

(499) In a vial, 2-iodo-1H-pyrrolo[2,3-b] pyridine 18a (200 mg, 0.82 mmol, 1 eq.) was dissolved in 8 ml of acetonitrile. Then 0.4 ml of acetic acid followed by 182 mg of Eschenmoser's salt (0.98 mmol, 1.2 eq.) were added. After sealing the vial, the reaction mixture is stirred for 20 h at room temperature. 15 ml of a 2M solution of potassium hydroxide is added slowly and then the organic phase was extracted with ethyl acetate (320 ml). The organic phases are combined and then dried over MgSO.sub.4, filtered through cotton and evaporated to dryness. Finally, the crude is triturated with pentane and then vacuum filtered to obtain compound 174 (190 mg, 77%) as a yellow solid. Rf=0.10 (methanol/dichloromethane=2/98) mp=142-144 C. IR (v, cm.sup.1, neat) 2957, 2932, 2851, 2812, 2768, 1603, 1580, 1514, 1489, 1448, 1407, 1369, 1354, 1328, 1287, 1273, 1248, 1206, 1167, 1147, 1121, 1094, 1036, 1004, 978, 905, 842. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 13.08 (s1, 1H), 8.41 (dd, J=4.9, 1.4 Hz, 1H), 8.09 (dd, J=7.9, 1.4 Hz, 1H), 7.11 (dd, J=7.9, 4.8 Hz, 1H), 3.60 (s 2H), 2.33 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 151.0 (Cq), 142.0 (CH), 127.4 (CH), 121.3 (Cq), 116.7 (Cq), 115.8 (CH), 82.9 (Cq) 56.1 (CH.sub.2), 45.4 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.10H.sub.12IN.sub.3 (M+H.sup.+): 302.0148, found: 302.0148.

Example 63.2 Synthesis of 4-((3-((dimethylamino)methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 175

(500) ##STR00373##

(501) Compound 175 was prepared according to procedure C2 and purified by flash column chromatography on silica gel (methanol/dichloromethane/ammonia=4/96/1). Brown solid (20%), Rf=0.15 (methanol/dichloromethane=4/96). mp=168-170 C. IR (v, cm.sup.1, neat) 2969, 2800, 2755, 2358, 1738, 1601, 1547, 1538, 1512, 1505, 1494, 1470, 1463, 1455, 1428, 1393, 1374, 1349, 1290, 1264, 1216, 1187, 1164, 1142, 1045, 1020, 1004, 979, 951. HRMS (+ESI) calculated for C.sub.21H.sub.23FN.sub.4 (M+H.sup.+): 351.1980; found: 351.1979.

Example 63.3 Synthesis of 4-((3-((dimethylamino)methyl)-6-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 177

(502) ##STR00374##

(503) Compound 177 was prepared according to procedure C2 and purified by flash column chromatography on silica gel (methanol/dichloromethane/ammonia=4/96/1). Greenish solid (36%), Rf=0.25 (methanol/dichloromethane=4/96). mp=182-184 C. IR (v, cm.sup.1, neat) 3157, 3072, 2893, 2205, 1605, 1541, 1511, 1432, 1273, 1224, 1183, 809, 763, 507. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 9.42 (s, 1H), 8.09 (t, J=8.0 Hz, 1H), 7.45 (d, J=8.7 Hz, 2H), 6.71 (m, 3H), 3.76 (s, 2H), 3.03 (s, 6H), 2.35 (s, 6H). .sup.13C NMR (101 MHz, DMSO-d6, 20 C.) 161.0 (d, J=238.0 Hz, Cq), 150.5 (Cq), 144.7 (d, J=18.3 Hz, CH), 132.7 (2CH), 132.5 (d, J=9.3 Hz, Cq)), 119.40 (d, J=4.4 Hz, Cq), 118.13 (d, J=2.7 Hz, Cq), 116.2 (Cq), 111.8 (2CH), 108.8 (Cq), 101.82 (d, J=37.8 Hz, CH), 97.7 (Cq), 78.0 (Cq), 54.1 (CH.sub.2), 45.4 (2CH.sub.3), 40.2 (2CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d6, 20 C.) . 76.0. HRMS (+ESI) calculated for C.sub.20H.sub.21FN.sub.4 (M+H.sup.+): 337.1823; found: 337.1822.

Example 64: 4-((3-((dimethylamino)methyl)-5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 179

(504) ##STR00375##

(505) 4-((3-((dimethylamino)methyl)-5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 179 was synthesized in 2 steps. Initially, the azaindole 180 is obtained by the Mannich reaction followed by the Sonogoshira reaction to obtain the desired final compound

(506) ##STR00376##

Example 64.1 Synthesis of 1-(5-fluoro-2-iodo-1H-pyrrolo[2,3-b]pyridin-3-yl)-N,N-dimethylmethanamine 180

(507) In a vial, 5-fluoro-2-iodo-1H-pyrrolo[2,3-b] pyridine 18 g (200 mg, 0.82 mmol, 1 eq.) was dissolved in 8 ml of acetonitrile. Then 0.4 ml of acetic acid, followed by 182 mg of salt of Esclienmoser (0.98 mmol, 1.2 eq.) were added. After sealing the vial, the reaction mixture is stirred for 20 h at room temperature. 15 ml of a 2M solution of potassium hydroxide is added slowly and then the organic phase was extracted with ethyl acetate (320 ml). The organic phases are combined and then dried over MgSO.sub.4, filtered through cotton and evaporated to dryness. Finally, the crude is triturated with pentane and then vacuum filtered to obtain compound 180 (180 mg, 77%) as a brown solid. Rf=0.10 (methanol/dichloromethane=2/98). mp=180-182 C. IR (v, cm.sup.1, neat) 2934, 2857, 2818, 2773, 2703, 1491, 152, 1395, 1368, 1333, 1322, 1295, 1261, 1250, 1218, 1183, 1168, 1146, 1068, 1006, 951, 871, 842. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.21 (s, 1H), 7.77 (dd, J=8.9, 2.4 Hz, 1H), 3.50 (s, 2H), 2.26 (s, 6H). .sup.13C NMR (250 MHz, CDCl.sub.3, 20 C.) 155.34 (d, J=242.4 Hz, Cq), 147.8 (Cq), 130.6 (d, J=30.2 Hz, CH), 121.02 (d, J=7.0 Hz, Cq), 117.10 (d, J=4.2 Hz, Cq), 113.27 (d, J=21.0 Hz, CH), 84.4 (Cq) 56.3 (CH.sub.2), 45.4 (2CH.sub.3). .sup.19F NMR (235 MHz, CDCl.sub.3, 20 C.) . 138.0. HRMS (+ESI) calculated for C.sub.10H.sub.12FIN.sub.3 (M+H.sup.+): 320.0054, found: 320.0054.

Example 64.2 Synthesis of 4-((3-((dimethylamino)methyl)-5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 179

(508) ##STR00377##

(509) Compound 177 was prepared according to procedure C2 and purified by flash column chromatography on silica gel (methanol/dichloromethane/ammonia=4/96/1). Brown solid (28%), Rf=0.25 (methanol/dichloromethane=4/96). mp=188-190 C. IR (v, cm.sup.1, neat) 2933, 2875, 2851, 2766, 2766, 2708, 1604, 1587, 1574, 1539, 1515, 1494, 1462, 1455, 1445, 1397, 1368, 1355, 1334, 1307, 1283, 1224, 1166, 1126, 1116, 1090, 1017, 982, 949, 906, 863507. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 9.89 (s, 1H), 8.20 (m, 1H), 7.75 (dd, J=8.9, 2.7 Hz, 1H), 7.44 (d, J=8.9 Hz, 2H), 6.68 (d, J=8.9 Hz, 2H), 3.72 (s, 2H), 3.02 (s, 6H), 2.32 (s, 6H). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 138.0. HRMS (+ESI) calculated for C.sub.20H.sub.21FN.sub.4 (M+H.sup.+): 337.1823; found: 337.1822.

Example 65: N-(2-fluoroethyl)-N-methyl-4-((3-methyl-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 181

(510) ##STR00378##

(511) N-(2-fluoroethyl)-N-methyl-4-((3-methyl-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 179 was synthesized in 6 steps. Initially, the azaindole 182 is obtained by five successive steps starting from 7-azaindole and the last step consists of the Sonogoshira reaction with alkyne to give the expected final compound

(512) ##STR00379##

Example 65.1 Synthesis of 3-bromo-1H-pyrrolo[2,3-b]pyridine 183

(513) At room temperature, N-bromosuccimide (1.65 g, 9.31 mmol, 1.1 eq.) was added on the 7-azaindole (1 g, 8.46 mmol, 1 eq.) dissolved in 20 ml of DCM. After 16 h stirring at room temperature, a saturated aqueous NaHCO.sub.3 (20 ml) was added. The aqueous phase is extracted with dichloromethane (2 times). Then the combined organic phases were dried over MgSO.sub.4 and concentrated under reduced pressure. The crude is purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=1/1) to obtain the compound 183 (1.6 g, 96%) as a brown solid. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 11.45 (br, 1H), 8.38 (dd, J=5.1, 1.2 Hz, 1H), 8.06 (dd, J=7.8, 1.2 Hz, 1H), 7.48 (s, 1H), 7.28 (dd, J=7.8, 5.1 Hz, 1H). CAS Number: 74420-15-8.

Example 65.2 Synthesis of 3-bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 184

(514) Under argon, 1 g of 3-bromo-1H-pyrrolo[2,3-b]pyridine 184 (5.07 mmol, 1.0 eq.) was dissolved in 30 ml of DCM. At room temperature, 49 mg of TBAB (0.15 mmol, 0.03 eq.) and 608 mg of iodine (15.21 mmol, 3.0 eq.) were added. Then, the reaction mixture was placed at 0 C. and then 0.81 ml of benzosulfonyle chloride was added dropwise. After 2 h of stirring at room temperature, 30 ml of water are added. The organic phases were extracted with dichloromethane (330 ml). The organic phases are combined and washed with a saturated NaCl solution and then dried over MgSO.sub.4, filtered through cotton and evaporated to dryness. The crude product is triturated with diethyl ether to obtain compound 184 (1.4 g, 82%) as an orange solid. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.48 (dd, J=4.8, 1.5 Hz, 1H), 8.24-8.17 (m, 2H), 7.82 (dd, J=8.0, 1.5 Hz, 1H), 7.79 (s, 1H), 7.60 (dd, J=7.5 Hz, 1H), 7.54-7.46 (m, 2H), 7.27 (m, 1H). CAS Number: 880769-95-9.

Example 65.3 Synthesis of 3-methyl-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 185

(515) 3-bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 184 (500 mg, 1.48 mmol) was dissolved in THF (10 ml) under argon. After degassing 10 minutes, Pd(PPh.sub.3) (85 mg, 0.074 mmol, 0.05 eq.) was then added and this is followed by addition of a solution of trimethylaluminium in toluene (2M, 1.48 ml, 2.96 mmol, 2.0 eq.) dropwise. Then the mixture is heated at 60 C. for 20 h. After cooling, 30 ml of a saturated solution of NaHCO.sub.3 are added dropwise. The organic phase was extracted with ethyl acetate (330 ml). The organic phases are combined and washed with saturated NaCl solution and then dried over MgSO.sub.4, filtered through cotton and evaporated to dryness. The crude was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=20/80) to obtain compound 185 (270 g, 67%) as a yellowish solid. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 11.45 (br, 1H), 8.38 (dd, J=5.1, 1.2 Hz, 1H), 8.06 (dd, J=7.8, 1.2 Hz, 1H), 7.48 (s, 1H), 7.28 (dd, J=7.8, 5.1 Hz, 1H), 2.32 (s, 3H). Reaxys Number: 28959361.

Example 65.4 Synthesis of 2-iodo-3-methyl-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 186

(516) Under an argon atmosphere, at a solution of 3-methyl-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 185 (270 mg, 0.99 mmol, 1.0 eq.) and of TMEDA (0.163 ml, 1.09 mmol, 1.1 eq.) in THF (0.1 M), cooled to 78 C., was added a solution of LDA (2M in THF, 0.6 ml, 1.19 mmol, 1.2 eq.) drop by drop.

(517) After 30 min, a solution of iodine (502.5 mg, 1.98 mmol, 2.0 eq.) in THF (0.5M) was slowly added via cannula to the reaction medium. After 30 min stirring at 78 C., 20 ml of water are added and the reaction medium is brought back to room temperature slowly. The organic phases were extracted with ethyl acetate (3 times 20 ml), combined, dried over MgSO.sub.4, extruding and then concentrated under reduced pressure. The crude was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=20/80) to obtain compound 186 (300 g, 76%) as a yellowish solid. Rf=0.10 (ethyl acetate/petroleum ether=20/80). mp=178-180 C. IR (v, cm.sup.1, neat) 2955, 2172, 2137, 2104, 2025, 1966, 1618, 1586, 1562, 1501, 1479, 1435, 1383, 1337, 1277, 1248, 1190, 1157, 1119, 1071, 1001, 973, 962, 933. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.37 (d, J=4.3 Hz, 1H), 8.14 (d, J=7.3 Hz, 2H), 7.68 (dd, J=8.7, 0.8 Hz, 1H), 7.57-7.35 (m, 3H), 7.12 (dd, J=7.8, 4.8 Hz, 1H), 2.22 (s, 3H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 6 150.5 (Cq) 144.7 (CH), 138.8 (Cq), 133.9 (CH), 128.9 (2CH), 127.9 (2CH), 126.8 (CH), 125.2 (Cq), 123.3 (Cq), 119.1 (CH), 80.0 (Cq), 13.5 (CH.sub.3). HRMS (+ESI) calculated for C.sub.14H.sub.11N.sub.2O.sub.2S (M+H.sup.+): 398.9658, found: 398.9657.

Example 65.5 Synthesis of 2-iodo-3-methyl-1H-pyrrolo[2,3-b]pyridine 182

(518) 2-iodo-3-methyl-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 186 (125 mg, 0.314 mmol, 1.0 eq.) was dissolved in 7 ml of dioxane. 45 mg of sodium t-butoxide (0.47 mmol, 1.5 eq.) were added. After 16 h at 80 C., the reaction medium was cooled to temperature and the solvent was evaporated under reduced pressure. The residue was dissolved in 30 ml ethyl acetate and 30 ml of water. Then, the organic phase is extracted with ethyl acetate (3 times). The combined organic phases were dried over MgSO.sub.4 and concentrated under reduced pressure. The crude was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=20/80) to obtain compound 182 (58 mg, 72%) as a yellowish solid. Rf=0.25 (ethyl acetate/petroleum ether=20/80). mp=188-190 C. IR (v, cm.sup.1, neat) 2707, 1580, 1455, 1405, 1381, 1336, 1325, 1281, 1205, 1130, 903, 784. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 11.93 (s, 1H), 8.13 (dd, J=4.6, 0.8 Hz, 1H), 7.87 (dd, J=7.5, 0.8 Hz, 1H), 7.01 (dd, J=7.5, 4.6 Hz, 1H), 2.19 (s, 3H). .sup.13C NMR (250 MHz, DMSO-d.sub.6, 20 C.) 151.0 (Cq), 142.9 (CH), 126.0 (CH), 120.5 (Cq), 115.7 (CH), 114.9 (Cq), 83.4 (Cq), 11.9 (CH.sub.3). HRMS (+ESI) calculated for C.sub.8H.sub.7IN.sub.2 (M+H.sup.+), found:

Example 65.6 Synthesis of N-(2-fluoroethyl)-N-methyl-4-((3-methyl-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 181

(519) ##STR00380##

(520) Compound 181 was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=20/80). Yellowish solid (28%), Rf=0.25 (ethyl acetate/petroleum ether=20/80). mp=212-214 C. IR (v, cm.sup.1, neat) 3033, 2910, 2777, 2358, 2341, 2196, 1603, 1581, 1539, 1513, 1446, 1434, 1407, 1368, 1352, 1284, 1266, 1233, 1212, 1180, 1132, 1076, 1036, 976. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 11.75 (s1, 1H), 8.29 (s1, 1H), 7.91 (d, J=7.8 Hz, 1H), 7.60 (s1, 1H), 7.39 (d, J=8.6 Hz, 2H), 7.07 (s1, 1H), 6.79 (d, J=8.6 Hz, 2H), 4.61 (dt, J=47.6, 5.0 Hz, 2H), 3.73 (dt, J=26.4, 5.0 Hz, 2H), 3.32 (s, 3H), 2.35 (s, 3H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 149.5 (Cq), 148.4 (Cq), 144.3 (Cq), 132.9 (2CH), 131.9 (Cq), 129.1 (Cq), 127.0 (CH), 118.1 (Cq), 114.3 (CH), 112.4 (2CH), 108.7 (CH), 97.4 (Cq), 83.2 (d, J=161.5 Hz, CH.sub.2) 79.6 (Cq), 51.8 (d, J=19.8 Hz, CH.sub.2), 38.9 (CH.sub.3), 9.9 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 221.3. HRMS (+ESI) calculated for C.sub.19H.sub.18FN.sub.3 (M+H+): 308.1557; found: 308.1558.

Example 66: N-(2-fluoroethyl)-N-methyl-4-((6-morpholino-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 187

(521) ##STR00381##

(522) N-(2-fluoroethyl)-N-methyl-4-((6-morpholino-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline N-(2-fluoroethyl)-N-methyl-4-((6-morpholino-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 187 was synthesized in 4 steps. Initially, the alkyne 188 was obtained in two successive steps starting from 6-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine 18j and then followed by the Buchwald reaction with an amine. Finally, the deprotection reaction provided the expected final compound

(523) ##STR00382## ##STR00383##

Example 66.1 Synthesis of 6-bromo-2-iodo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 189

(524) Under argon, 6-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine 18j (500 mg, 1.55 mmol, 1 eq.) was dissolved in 10 ml of DMF. At 0 C., NaH (50% in mineral oil, 89 mg, 1.86 mmol, 1.2 eq.) was added portionwise. After 1 h stirring, SEMCl (0.33 ml, 1.86 mmol, 1.2 eq.) was added dropwise. After 2 hours of reaction, 10 ml of water was added slowly. The organic phases are extracted with ethyl acetate (310 ml). The combined organic phases were washed with NaCl, dried over MgSO.sub.4 and concentrated reduced pressure. The crude was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=20/80) to obtain compound 189 (603 g, 86%) as a colorless oil. Rf=0.9 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 2949, 1568, 1463, 1448, 1418, 1394, 1376, 1310, 1259, 1246, 1217, 1202, 1119, 1110, 1076, 992, 969, 943, 915, 855. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.65 (d, J=8.1 Hz, 1H), 7.20 (d, J=8.1 Hz, 1H), 6.82 (s, 1H), 5.68 (s, 2H), 3.63-3.54 (m, 2H), 0.98-0.88 (m, 2H), 0.0 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 148.5 (Cq), 135.1 (Cq), 129.2 (CH), 120.6 (CH), 112.2 (CH), 91.6 (Cq), 83.8 (Cq), 73.1 (CH.sub.2), 66.4 (CH.sub.2), 17.8 (CH.sub.2), 1.46 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.13H.sub.18BrIN.sub.2OSi (M+H.sup.+): 452.9489 found: 452.9487.

Example 66.2 Synthesis of 4-((6-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 188

(525) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=10/90). Yellowish solid (63%), mp 106-108 C., Rf=0.7 (dichloromethane). IR (v, cm.sup.1, neat) 2891, 2198, 1607, 1557, 1538, 1510, 1447, 1417, 1360, 1293, 1266, 1243, 1223, 1186, 1130, 1114, 1072, 1044, 979, 933, 895. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.68 (d, J=7.9 Hz, 1H), 7.44 (d, J=8.7 Hz, 2H), 7.25 (d, J=7.9 Hz, 1H), 6.76-6.62 (m, 3H), 5.77 (s, 2H), 4.62 (dt, J=47.1, 5.1 Hz, 2H), 3.78-3.61 (m, 4H), 3.07 (s, 3H), 1.01-0.91 (m, 2H), 0.00 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 149.2 (Cq), 147.7 (Cq), 135.9 (Cq), 133.0 (2CH), 130.3 (CH), 123.6 (Cq), 120.7 (CH), 118.9 (Cq), 111.7 (2CH.sub.2), 109.2 (Cq), 105.8 (CH), 98.0 (Cq), 81.60 (d, J=170.2 Hz, CH.sub.2), 78.2 (Cq), 71.1 (CH.sub.2), 66.6 (CH.sub.2), 52.35 (d, J=21.1 Hz, CH.sub.2), 39.0 (CH.sub.3), 17.8 (CH.sub.2), 0.00 (3CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 222.3. HRMS (+ESI) calculated for C.sub.24H.sub.29BrFN.sub.3OSi (M+H.sup.+): 502.1320, found: 502.1318.

Example 66.3 Synthesis of N-(2-fluoroethyl)-N-methyl-4-((6-morpholino-1-((2-(trimethylsilyl)ethoxy) methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 190

(526) Under argon, Pd(OAc).sub.2 (0.05 eq) and Xantphos (0.075 mmol) were added to a degassed anhydrous dioxane solution of 0.05 M concentration containing 4-((6-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 188 (1.0 eq.), morpholine (1.0 eq.) and CsCO.sub.3 (1.2 eq.). After 1 h30 at 110 C., the solvent was evaporated under reduced pressure. Then, the reaction mixture was concentrated under reduced pressure before being purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=20/80) to get the compound 190 (21 mg, 52%) as a greenish solid. Rf=0.1 (dichloromethane). mp: 110-112 C. IR (v, cm.sup.1, neat) 2952, 2890, 2851, 1602, 1568, 1538, 1507, 1489, 1443, 1431, 1403, 1374, 1338, 1324, 1293, 1246, 1229, 1190, 1156, 1120, 1104, 1071, 1046, 980, 941, 907. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.19 (s, 1H), 7.49-7.37 (m, 3H), 6.75-6.60 (m, 3H), 5.77 (s, 2H), 4.62 (dt, J=47.1, 5.1 Hz, 2H), 3.98-3.87 (m, 4H), 3.76-3.63 (m, 4H), 3.19-3.12 (m, 3H), 3.07 (s, 3H), 0.92 (m 2H), 0.08 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 154.8 (Cq), 149.0 (Cq), 144.2 (Cq), 143.5 (Cq), 137.7 (CH), 132.9 (2CH), 123.8 (Cq), 120.2 (Cq), 115.6 (CH), 111.8 (2CH), 109.5 (Cq), 105.2 (CH), 97.5 (Cq), 81.60 (d, J=170.2 Hz, CH.sub.2), 78.7 (Cq), 71.2 (CH.sub.2), 67.0 (2CH.sub.2), 66.2 (CH.sub.2), 52.5 (d, J=21.1 Hz, CH.sub.2), 51.6 (2CH.sub.2), 39.0 (CH.sub.3), 17.8 (CH.sub.2), 0.00 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.28H.sub.37FN.sub.4O.sub.2Si (M+H.sup.+): 509.2739, found: 509.2743.

Example 66.4 Synthesis of N-(2-fluoroethyl)-N-methyl-4-((6-morpholino-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 187

(527) ##STR00384##

(528) At room temperature and under argon, a solution of TBAF in THF (C=1 M, 0.19 ml, 0.19 mmol, 5.0 eq.) was added dropwise to the reaction medium containing N-(2-fluoroethyl)-N-methyl-4-((6-morpholino-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 190 (20 mg, 0.04 mmol, 1.0 eq.) and ethylenediamine (0.004 ml, 0.06 mmol, 1.2 eq.) diluted in 2 ml of THF. After 24 h at 80 C., the reaction mixture was cooled and 10 ml of water, followed by 10 ml of ethyl acetate are successively added. The organic phases were extracted 3 times with ethyl acetate. Then, they were combined, dried with MgSO.sub.4, filtered through cotton and evaporated under reduced pressure. Finally, the crude was purified by flash column chromatography on silica gel with eluent (ethyl acetate/petroleum ether=20/80) to get the final compound (7 mg, 46%) as a greenish solid. Rf=0.5 (ethyl acetate/petroleum ether=20/80). mp>260 C. IR (v, cm.sup.1, neat) 3289, 2918, 2851, 1604, 1573, 1539, 1506, 1449, 1424, 1374, 1293, 1257, 1230, 1184, 1136, 1108, 1067, 1055, 1038, 992, 900. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.39 (s, 1H), 7.71 (d, J=8.8 Hz, 1H), 7.42 (m, 2H), 6.69 (d, J=8.5 Hz, 1H), 6.59 (s, 1H), 4.69 (m, 1H), 4.57 (m, 1H), 3.87 (m, 4H), 3.74 (m, 1H), 3.68 (m, 1H), 3.55 (m, 4H), 3.08 (s, 3H). .sup.13C NMR DEPT (101 MHz, CDCl.sub.3, 20 C.) 131.4 (2CH), 130.3 (CH), 111.6 (2CH), 106.3 (CH), 101.9 (CH), 81.60 (d, J=170.2 Hz, CH.sub.2), 78.7 (Cq), 65.0 (2CH.sub.2), 52.5 (d, J=21.1 Hz, CH.sub.2), 46.4 (2CH.sub.2), 39.0 (CH.sub.3). HRMS (+ESI) calculated for C.sub.22H.sub.23FN.sub.4O (M+H+): 379.1924, found: 379.1928.

Example 67: 1-(6-bromo-2-((4-(dimethylamino)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridin-1-yl)ethan-1-one 191

(529) ##STR00385##

(530) 1-(6-bromo-2-((4-(dimethylamino)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridin-1-yl)ethan-1-one 191 was synthesized in 2 steps. Initially, 6-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine 18j was protected with an acetate type protecting group and the the Sonogoshira reaction was performed to get the final compound. Then radiolabeling tests with fluorine 18 may be made on the position 6 of azaindolique nucleous to give after deprotection the radiolabelled compound 22f.

(531) ##STR00386##

Example 67.1 Synthesis of 1-(6-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridin-1-yl)ethan-1-one 192

(532) Under argon, 6-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine 18j (200 mg, 0.62 mmol, 1 eq.) was dissolved in 5 ml of DMF. Acetic anhydride (0.088 ml, 0.93 mmol, 1.5 eq.) and triethylamine (0.129 ml, 0.93 mmol, 1 0.5 eq) were added successively. After 18 h stirring at room temperature, 10 ml of water was added slowly. The organic phases were extracted with ethyl acetate (310 ml). The combined organic phases were washed with NaCl, dried over MgSO.sub.4, filtered and concentrated under reduced pressure. The crude is purified by flash column chromatography on silica gel (dichloromethane/petroleum ether=20/40) to provide compound 192 (186 mg, 82%) as a white solid Rf=0.6 (dichloromethane), mp:126-128 C. IR (v, cm.sup.1, neat) 1718, 1590, 1558, 1489, 1429, 1404, 1368, 1294, 1254, 1218, 1205, 1134, 1113, 1090, 1025, 991, 905, 829, 807. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.62 (d, J=8.1 Hz, 1H), 7.34 (d, J=8.1 Hz, 1H), 6.99 (s, 1H), 3.05 (s, 3H). .sup.13C NMR DEPT (250 MHz, CDCl.sub.3, 20 C.) 129.2 (CH), 122.9 (CH), 119.7 (CH), 27.9 (CH.sub.3). HRMS (+ESI) calculated for C.sub.9H.sub.6BrIN.sub.2O (M+Na+): 386.8600, found: 386.8599.

Example 67.2 Synthesis of 1-(6-bromo-2-((4-(dimethylamino)phenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridin-1-yl)ethan-1-one 191

(533) ##STR00387##

(534) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (dichloromethane/petroleum ether=50/50). Yellowish solid (87%), mp 194-196 C., Rf=0.5 (dichloromethane/petroleum ether=40/60). IR (v, cm.sup.1, neat) 2918, 2852, 2188, 1728, 1604, 1561, 1541, 1508, 1448, 1431, 1393, 1364, 1322, 1305, 1290, 1258, 1221, 1185, 1131, 1099, 1067, 1037, 1010, 936, 900. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.64 (d, J=8.0 Hz, 1H), 7.45 (d, J=8.9 Hz, 2H), 7.33 (d, J=8.0 Hz, 1H), 6.77 (s, 1H), 6.63 (d, J=8.9 Hz, 2H), 3.03 (s, 3H), 2.98 (s, 6H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 169.0 (Cq), 150.5 (Cq), 146.6 (Cq). 135.5 (Cq), 133.0 (2CH), 130.2 (CH), 123.0 (CH), 122.7 (Cq), 120.9 (Cq), 111.7 (2CH), 111.2 (CH), 109.0 (Cq), 98.9 (Cq), 79.8 (Cq), 40.1 (2CH.sub.3), 27.4 (CH.sub.3). HRMS (+ESI) calculated for C.sub.19H.sub.16BrN.sub.3O (M+Na.sup.+): 404.0368, found: 404.0369.

Example 68: N-(2-fluoroethyl)-N-methyl-4-((5-morpholino-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 193

(535) ##STR00388##

(536) N-(2-fluoroethyl)-N-methyl-4-((6-morpholino-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl) aniline 193 was synthesized in 4 steps. Initially, the alkyne 194 was obtained in 2 successive steps starting from 5-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine 18k then the Buchwald reaction with an amine is carried out. Finally, a deprotection reaction led to the expected final compound.

(537) ##STR00389## ##STR00390##

Example 68.1 Synthesis of 5-bromo-2-iodo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 195

(538) Under argon, 5-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine 18k (594 mg, 1.84 mmol, 1 eq.) was dissolved in 10 ml of DMF. At 0 C., NaH (50% in mineral oil, 105 mg, 2.21 mmol, 1.2 eq.) was added portionwise. After 1 h of stirring, SEMCl (0.39 ml, 2.21 mmol, 1.2 eq.) was added dropwise. After 2 hours of reaction, 10 ml of water were added slowly. The organic phases were extracted with ethyl acetate (310 ml). The combined organic phases were washed with NaCl, dried over MgSO.sub.4, filtered and concentrated under reduced pressure. The crude was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=5/95) to afford compound 195 (534 g, 64%) as a colorless oil. Rf=0.9 (ethyl acetate/petroleum ether=5/95). IR (v, cm.sup.1, neat) 2949, 1568, 1463, 1448, 1418, 1394, 1376, 1310, 1259, 1246, 1217, 1202, 1119, 1110, 1076, 992, 969, 943, 915, 855. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.27 (d, J=2.3 Hz, 1H), 7.93 (d, J=2.3 Hz, 1H), 6.77 (s, 1H), 5.68 (s, 2H), 3.63-3.54 (m, 2H), 0.98-0.88 (m, 2H), 0.00 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 147.6 (Cq), 143.6 (CH), 129.1 (CH), 123.3 (Cq), 112.7 (Cq), 111.3 (CH), 91.6 (Cq), 85.8 (Cq), 73.1 (CH.sub.2), 66.4 (CH.sub.2), 17.8 (CH.sub.2), 1.46 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.13H.sub.18BrIN.sub.2OSi (M+H.sup.+): 452.9489 found: 452.9487.

Example 68.2 Synthesis of 4-((5-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 194

(539) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=10/90). Yellowish solid (63%). mp 84-86 C., Rf=0.25 (ethyl acetate petroleum ether=20/80). IR (v, cm.sup.1, neat) 2891, 2198, 1607, 1557, 1538, 1510, 1447, 1417, 1360, 1293, 1266, 1243, 1223, 1186, 1130, 1114, 1072, 1044, 979, 933, 895. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.37 (d, J=2.3 Hz, 1H), 7.97 (d, J=2.3 Hz, 2H), 7.44 (d, J=7.9 Hz, 1H), 6.76-6.62 (m, 3H), 5.78 (s, 2H), 4.62 (dt, J=47.1, 5.1 Hz, 2H), 3.78-3.61 (m, 4H), 3.00 (s, 3H), 1.01-0.91 (m, 2H), 0.00 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 149.2 (Cq), 146.6 (Cq), 144.5 (CH), 133.0 (2CH), 130.2 (CH), 124.9 (Cq), 121.8 (Cq), 112.8 (Cq), 112.8 (2CH.sub.2), 109.0 (Cq), 1054.9 (CH), 98.0 (Cq), 81.60 (d, J=170.2 Hz, CH.sub.2), 78.2 (Cq), 71.1 (CH.sub.2), 66.6 (CH.sub.2), 52.35 (d, J=21.1 Hz, CH.sub.2), 39.0 (CH.sub.3), 17.8 (CH.sub.2), 0.00 (3CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) . 222.3. HRMS (+ESI) calculated for C.sub.24H.sub.29BrFN.sub.3OSi (M+H.sup.+): 502.1320, found: 502.1318.

Example 68.3 Synthesis of N-(2-fluoroethyl)-N-methyl-4-((5-morpholino-1-((2-(trimethylsilyl)ethoxy) methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 196

(540) Under argon, Pd.sub.2(dba).sub.3 (2 mg, 0.002 mmol, 0.02 eq.) and Xantphos (4 mg, 0.006 mmol, 0.06 eq.) were added to a degassed anhydrous toluene solution of 0.1 M concentration containing the 4-((5-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 188 (50 mg, 0.1 mmol, 1.0 eq.), morpholine (0.012 ml, 0.12 mmol, 1.2 eq.) and the tBuONa (14 mg, 0.15 mmol, 1.5 eq.). After 2 h at 110 C., the solvent was evaporated under reduced pressure. Then, the reaction mixture was concentrated under reduced pressure before being purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=20/80) to get compound 196 (23 mg, 45%) as a greenish oil. Rf=0.25 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 2952, 2890, 2851, 1602, 1568, 1538, 1507, 1489, 1443, 1431, 1403, 1374, 1338, 1324, 1293, 1246, 1229, 1190, 1156, 1120, 1104, 1071, 1046, 980, 941, 907. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.19 (s, 1H), 7.43 (d, J=8.6 Hz, 2H), 7.39 (s, 1H), 6.72-6.61 (m, 3H), 5.77 (s, 2H), 4.62 (dt, J=47.2, 5.1 Hz, 2H), 3.94-3.88 (m, 4H), 3.73 (m, 4H), 3.14 (m, 4H), 3.07 (s, 3H), 0.97-0.89 (m, 2H), 0.08 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 148.9 (Cq), 144.00 (Cq), 143.4 (Cq), 137.5 (CH), 132.8 (2CH), 123.6 (Cq), 120.0 (Cq), 115.5 (CH), 111.6 (2CH.sub.2), 109.3 (Cq), 105.0 (CH), 97.3 (Cq), 81.60 (d, J=170.2 Hz, CH.sub.2), 78.2 (Cq), 71.0 (CH.sub.2), 66.9 (2CH.sub.2), 66.1 (CH.sub.2), 52.3 (d, J=21.1 Hz, CH.sub.2), 52.1 (2CH.sub.2), 38.9 (CH.sub.3), 17.7 (CH.sub.2), 0.00 (3CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 222.0 HRMS (+ESI) calculated for C.sub.28H.sub.37FN.sub.4O.sub.2Si (M+H.sup.+): 509.2739, found: 509.2743.

Example 68.4 Synthesis of N-(2-fluoroethyl)-N-methyl-4-((5-morpholino-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 193

(541) ##STR00391##

(542) At room temperature and under argon, a solution of TBAF in THF (C=1 M, 0.23 ml, 0.23 mmol, 5.0 eq.) was added dropwise to the reaction medium containing N-(2-fluoroethyl)-N-methyl-4-((6-morpholino-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 190 (23 mg, 0.045 mmol, 1.0 eq.) and ethylenediamine (0.005 ml, 0.07 mmol, 1.2 eq.) diluted in 2 ml of THF. After 48 h at 80 C., the reaction mixture was cooled and 10 ml of water, then 10 ml of ethyl acetate are successively added. The organic phases were extracted 3 times with ethyl acetate (30 ml), combined, dried over MgSO.sub.4 filtered through cotton and evaporated under reduced pressure. Finally, the crude is purified by flash column chromatography on silica gel with eluent (ethyl acetate/petroleum ether=30/70) to get the final compound (7 mg, 41%) as a solid greenish. Rf=0.1 (ethyl acetate/petroleum ether=30/70). mp>260 C. IR (v, cm.sup.1, neat) 3289, 2918, 2851, 1604, 1573, 1539, 1506, 1449, 1424, 1374, 1293, 1257, 1230, 1184, 1136, 1108, 1067, 1055, 1038, 992, 900. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 9.01 (s, 1H), 8.15 (s, 1H), 7.45 (m, 3H), 6.67 (m, 3H), 4.62 (m, 2H), 3.93 (m, 4H), 3.70 (m, 2H), 3.16 (m, 4H), 3.07 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 149.1 (Cq), 143.9 (Cq), 143.8 (Cq), 137.3 (CH), 132.9 (2CH), 123.4 (Cq), 121.7 (Cq), 116.0 (CH), 111.8 (2CH.sub.2), 109.3 (Cq), 105.4 (CH), 94.8 (Cq), 81.60 (d, J=170.2 Hz, CH.sub.2), 78.2 (Cq), 67.1 (2CH.sub.2), 52.3 (d, J=21.1 Hz, CH.sub.2), 51.6 (2CH.sub.2), 38.9 (CH.sub.3). .sup.19F NMR (376 MHz, CDCl.sub.3, 20 C.) . 222. HRMS (+ESI) calculated for C.sub.8H.sub.7IN.sub.2 (M+H.sup.+): 379.1929, found: 379.1928.

Example 69: 4-(2-((4-((2-fluoroethyl)(methyl)amino)phenyl)ethynyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)benzonitrile 198

(543) 4-((5-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N-(2-fluoroethyl)-N-methylaniline 198 was obtained from 194 by a Suzuki reaction with the corresponding boronic acid. Deprotection of the silyl derivative will give the final deprotected product 197

(544) ##STR00392##

(545) Under argon, 4-((5-bromo-1-((2-(trimethylsilyl) ethoxy) methyl)-1H-pyrrolo[2,3-b] pyridin-2-yl) ethynyl)-N-(2-fluoroethyl)-N-methylaniline 194 (25 mg, 0.05 mmol, 1 eq.) was dissolved in a mixture toluene/EtOH (1/1) then the addition of 4-cyanophenylboronic acid (9 mg, 0.06 mmol, 1.2 eq.) and K.sub.2CO.sub.3 (21 mg, 0.15 mmol, 3 eq.) is performed. Then, the reaction medium was degassed for 10 minutes before adding [Pd(PPh.sub.3).sub.4] (5.8 mg, 0.005 mmol, 0.1 eq.). The reaction mixture was heated to 90 C. for 7 h. After cooling, the solvents are evaporated under reduced pressure. Finally, the crude is purified by flash column chromatography on silica gel with eluent (ethyl acetate/petroleum ether=20/80) to get the final compound (14 mg, 54%) as a yellow is solid h. Rf=0.2 (dichloromethane) mp. 158-160 C. IR (v, cm.sup.1, neat) 2949, 2224, 2197, 1606, 1541, 1514, 1474, 1450, 1422, 1377, 1353, 1317, 1291, 1261, 1247, 1215, 1196, 1182, 1135, 1114, 1097, 1066, 1047, 982, 941, 897, 857. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.59 (d, J=1.6 Hz, 1H), 8.04 (d, J=1.6 Hz, 1H),), 7.75 (m, 4H), 7.45 (d, J=8.1 Hz, 2H), 6.79 (s, 1H), 6.69 (d, J=8.1 Hz, 2H), 5.85 (s, 2H), 4.63 (dt, J=47.2, 5.1 Hz, 2H), 3.71 (m, 4H), 3.08 (s, 3H), 0.97-0.89 (m, 2H), 0.08 (s, 9H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 149.2 (Cq), 148.3 (Cq), 144.1 (Cq), 143.2 (CH), 133.0 (2CH), 132.8 (2CH), 128.7 (Cq), 127.8 (2CH), 126.8 (CH), 124.8 (Cq), 120.0 (Cq), 118.8 (Cq), 111.8 (2CH), 110.7 (Cq), 109.1 (Cq), 105.9 (CH), 98.4 (Cq), 81.60 (d, J=170.2 Hz, CH.sub.2), 78.3 (Cq), 71.0 (CH.sub.2), 66.5 (CH.sub.2), 52.3 (d, J=21.1 Hz, CH.sub.2), 38.9 (CH.sub.3), 17.8 (CH.sub.2), 0.00 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.31H.sub.33FN.sub.4OSi (M+H.sup.+): 398.9658, found: 398.9657.

Example 70: N,N-dimethyl-4-((5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 199

(546) ##STR00393##

(547) N,N-dimethyl-4-((5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 193 was synthesized in 4 steps. Initially, the alkyne 201 was obtained in 2 successive steps starting from 5-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine 18k and the Sonogashira reaction with the corresponding alkyne was carried out and finally the deprotection reaction provided the expected final compound. This will be a precursor in order to use in radiolabeling

(548) ##STR00394## ##STR00395##

Example 70.1 Synthesis of 5-bromo-1-(tert-butyldimethylsilyl)-2-iodo-1H-pyrrolo[2,3-b]pyridine 201

(549) Under argon, 5-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine 18k (230 mg, 0.71 mmol, 1 eq.) was dissolved in 10 ml of THF. At 0 C., NaH (50% in mineral oil, 41 mg, 0.86 mmol, 1.2 eq.) was added portionwise. After 30 h stirring at temperature, the mixture was returned to 0 C. and TBDMSCI (129 mg, 0.86 mmol, 1.2 eq.) was added portionwise. Then the mixture was carried out at 80 C. for 2 h30. After cooling to 0 C., 10 ml of water was added slowly and the organic phases were extracted with the ethyl acetate (310 ml). The combined organic phases were washed with NaCl, dried over MgSO.sub.4, filtered and concentrated under reduced pressure. The crude was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=5/95) to provide compound 201 (117 g, 38%) as a colorless oil. Rf=0.9 (ethyl acetate/petroleum ether=5/95). IR (v, cm.sup.1, neat) 2951, 2925, 2854, 1587, 1541, 1484, 1460, 1444, 1353, 1339, 1307, 1253, 1215, 1175, 1114, 1066, 997, 917, 846. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.16 (d, J=2.3 Hz, 1H), 7.82 (d, J=2.3 Hz, 1H), 6.80 (s, 1H), 0.94 (s, 9H), 0.81 (s, 6H). .sup.13C NMR DEPT (63 MHz, CDCl.sub.3, 20 C.) 142.2 (CH), 127.7 (CH), 116.7 (CH), 27.1 (3CH.sub.2), 0.65 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.13H.sub.18BrN.sub.2Si (M+H.sup.+): 436.9540 found: 436.9538.

Example 70.2 Synthesis of 4-((5-bromo-1-(tert-butyldimethylsilyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 200

(550) The compound was prepared according to procedure C2 and purified by flash column chromatography on silica gel (dichloromethane/petroleum ether=20/80). Yellowish amorphous solid (62%), Rf=0.5 (ethyl acetate/petroleum ether=20/80). IR (v, cm.sup.1, neat) 2952, 2890, 2851, 1603, 1568, 1538, 1507, 1489, 1443, 1431, 1403, 1374, 1338, 1324, 1293, 1246, 1229, 1191, 1157, 1120, 1104, 1071, 1046, 980, 942, 907. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.28 (d, J=2.3 Hz, 1H), 7.91 (d, J=2.3 Hz, 2H), 6.76-6.62 (m, 3H), 3.00 (s, 6H), 0.99 (s, 9H), 0.82 (s, 6H). .sup.13C NMR DEPT (101 MHz, CDCl.sub.3, 20 C.) 143.4 (CH), 132.4 (2CH), 128.9 (CH), 111.9 (2CH.sub.2), 109.7 (CH), 40.2 (2CH.sub.3), 26.7 (3CH.sub.3), 1.58 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.2H.sub.28BrN.sub.3Si (M+H.sup.+): 454.1308, found: 454.1309.

Example 70.3 Synthesis of N,N-dimethyl-4-((5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 199

(551) ##STR00396##

(552) Under argon, 4-((5-bromo-1-(tert-butyldimethylsilyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 200 (50 mg, 0.11 mmol, 1.0 eq.) was dissolved in dioxane (1 ml) followed by the addition of bis (pinacolato) diboron (56 mg, 0.22 mmol, 2.0 eq.) and KOAc (32 mg, 0.33 mmol, 3.0 eq.) was carried out. Then, the reaction medium is degassed for 10 minutes before adding Pd(dppf).sub.2Cl.sub.2.DCM (9.0 mg, 0.011 mmol, 0.1 eq.). The reaction mixture was heated at 100 C. for 4 h.

(553) After cooling, the solvent was evaporated under reduced pressure. Finally, the crude was purified by flash column chromatography on silica gel with eluent (dichloromethane/petroleum ether=30/70) to provide the intermediate. Then the crude product was directly dissolved in 5 ml of THF. At 0 C., a solution of TBAF in THF (C=1 M, 0.05 ml, 0.05 mmol, 0.2 eq.) was added dropwise. After 40 minutes at 0 C., 10 ml of water and 10 ml of ethyl acetate were successively added. The organic phases were extracted 3 times with ethyl acetate, combined, dried with MgSO.sub.4, filtered through cotton and evaporated under reduced pressure. The crude was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=20/80) to procided the compound 199 (10 mg, 64%) as a yellow solid. Rf=0.1 (ethyl acetate/petroleum ether=10/90). mp>260 C. IR (v, cm.sup.1, neat) 3291, 2962, 2930, 2853, 2102, 1606, 1511, 1463, 1434, 1373, 1356, 1336, 1273, 1245, 1227, 1185, 1141, 1093, 1023, 935. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.20 (s, 1H), 8.46 (s, 1H), 8.18 (s, 1H), 7.39 (d, J=8.6 Hz, 2H), 6.74 (m, 3H), 2.97 (s, 6H), 1.32 (s, 12H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 150.9 (Cq), 150.3 (Cq), 149.8 (Cq), 135.2 (CH), 133.0 (2CH), 120.9 (Cq), 120.9 (Cq), 119.9 (Cq), 112.5 (2CH), 110.7 (Cq), 107.9 (Cq), 106.0 (CH), 95.4 (Cq), 84.1 (2Cq), 80.6 (Cq), 40.2 (2CH.sub.3), 25.2 (4CH.sub.3). HRMS (+ESI) calculated for C.sub.23H.sub.26BN.sub.3O.sub.2 (M+H.sup.+): 388.2190, found: 388.2193.

Example 71: N,N-dimethyl-4-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 202

(554) ##STR00397##

(555) N,N-dimethyl-4-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 202 was synthesized in 6 steps. Initially, the alkyne 204 was obtained in 5 successive steps starting from 4-bromo-1H-pyrrolo[2,3-b]pyridine and the Sonogashira reaction with the corresponding alkyne was carried out and finally the deprotection reaction provided the expected final compound. The compounds 207 and 202 are precursors for radiolabeling

(556) ##STR00398## ##STR00399## ##STR00400##

Example 71. Synthesis of 4-bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 205

(557) To a solution of NaH (1.46 g, 30.4 mmol, 1.2 eq.) in THF under argon and at 0 C. was slowly added a solution of 4-bromo-7-azaindole (5 g, 25.4 mmol, 1.0 eq.) in THF (1 M). The mixture was stirred at room temperature for 30 min. Return to 0 C., benzenesulfonyl chloride (3.5 ml, 27.9 mmol, 1.1 eq.) was added drop by drop. After 3 h stirring at room temperature the mixture was poured into a vial filled with ice. Once the medium back to room temperature, the phases were separated. The aqueous phase was extracted with ethyl acetate. The combined organic phases were washed with NaCl, dried over MgSO.sub.4 and concentrated under reduced pressure. The crude product was triturated with pentane and vacuum filtered to obtain compound 205 (7.2 g, 84%) as a brown solid. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 8.18 (d, J=7.8 Hz, 3H), 7.52 (m, 4H), 7.30 (m, 1H), 7.02 (s, 1H). CAS Number: 889939-25-7.

Example 71.2 Synthesis of 4-bromo-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 205

(558) Under argon atmosphere, to a solution of 4-bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b] pyridine 205 (7 g, 0.99 mmol, 1.0 eq.) and TMEDA (3.42 ml, 22.8 mmol, 1.1 eq.) in THF (0.1 M), cooled to 78 C., was added a solution of LDA (2M in THF, 12.5 ml, 24.8 mmol, 1.2 eq.) dropwise. After 30 min, a solution of iodine (1.5 1 g, 45.5 mmol, 2.2 eq.) In THF (0.5M) was slowly added via cannula to the reaction medium. After 30 min stirring at 78 C., 20 ml of water are additonnes and the reaction medium is brought back to room temperature slowly. The organic phases are extracted with ethyl acetate (3 times 20 ml), combined, dried over MgSO.sub.4, filtered and then concentrated under reduced pressure. The crude was purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80) to yield compound 205 (8.1 g, 76%) as a brown solid. Rf (0.10 (ethyl acetate/petroleum ether=20/80). M.P. 144-146 C. IR (v, cm.sup.1, neat) 3383, 2359, 1635, 1588, 1567, 1485, 1449, 1430, 1370, 1333, 1275, 1235, 1207, 1175, 1129, 1114, 1087, 1011, 918, 826, 755, 723, 697, 684, 623, 585, 557, 537, 502. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.19 (t, J=6.5 Hz, 3H), 7.65-7.44 (m, 3H), 7.32 (d, J=5.5 Hz, 1H), 7.05 (s, 1H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 149.1 (Cq), 144.7 (CH), 138.3 (Cq), 134.4 (CH), 129.1 (2CH), 128.2 (2CH), 125.3 (2Cq), 123.7 (Cq), 122.5 (CH), 119.6 (CH). HRMS (+ESI) calculated for C.sub.13H.sub.9BrIN.sub.2O.sub.2S (M+H+): 464.8587, found: 464.8581.

Example 71.3 Synthesis of 4-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine 203

(559) 4-bromo-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-e]pyridine 205 (8.1 g, 17.5 mmol, 1.0 eq.) was dissolved in 250 ml of dioxane and 2.6 g of tert sodium t-butoxide (26.3 mmol, 1.5 eq.) were added. After 16 h at 80 C., the reaction medium is cooled to temperature and the solvent was evaporated under reduced pressure. The residue was dissolved in 100 ml of ethyl acetate and 100 ml of water are added. Then, the organic phase is extracted with ethyl acetate (3 times 20 ml). The combined organic phases were dried over MgSO.sub.4 and concentrated under reduced pressure. The crude is triturated with dichloromethane and then vacuum filtration allows to produce compound 203 (58 g, 72%) as a yellowish solid. Rf=0.25 (ethyl acetate/petroleum ether=20/80). Mp>260 C. IR (v, cm.sup.1, neat) 3898, 3851, 3819, 3800, 3749, 3742, 3731, 3687, 3674, 3668, 3646, 3627, 3565, 3099, 3019, 2930, 2844, 2798, 2588, 2216, 1912, 1595, 1567, 1473, 1406, 1382, 1330, 1282, 1263, 1206, 1120, 1098, 964, 953, 920, 813, 751, 670, 621, 603, 536, 524, 517, 506. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.60 (s, 1H), 7.97 (d, J=5.2 Hz, 1H), 7.26 (d, J=5.2 Hz, 1H), 6.62 (s, 1H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 150.7 (Cq), 143.5 (CH), 123.2 (Cq), 121.9 (Cq), 119.3 (CH), 109.4 (CH), 83.2 (Cq). HRMS (+ESI) calculated for C.sub.7H.sub.4BrIN.sub.2 (M+H.sup.+): 322.8675, found: 322.8673.

Example 71.4 Synthesis of 4-bromo-1-(tert-butyldimethylsilyl)-2-iodo-1H-pyrrolo[2,3-b]pyridine 206

(560) Under argon, 4-bromo-2-iodo-1H-pyrrolo[2,3-b]pyridine 203 (386 mg, 1.19 mmol, 1.0 eq.) was dissolved in 20 ml of THF. At 0 C., NaH (50% in mineral oil, 68 mg, 1.43 mmol, 1.2 eq.) was added portionwise. After stirring for 30 minutes at temperature, the mixture was returned to 0 C. and TBDMSCl (215 mg, 1.43 mmol, 1.2 eq.) Was added in portions. Then the mixture is at 80 C. for 2 h30. After cooling to 0 C., 10 ml of water are slowly added and the organics were extracted with ethyl acetate (310 ml). The combined organic phases were washed with NaCl, dried over MgSO.sub.4, filtered and concentrated under reduced pressure. The crude is purified by column flash chromatographie on silicagel (ethyl acetate/petroleum ether=5/95) to yield compound 205 (300 g, 57%) as a colorless oil. Rf=0.9 (ethyl acetate/petroleum ether=5/95 IR (v, cm.sup.1-, neat) 2951, 2925, 2854, 1587, 1541, 1484, 1460, 1444, 1353, 1339, 1307, 1253, 1215, 1175, 1114, 1066, 997, 917, 846. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 7.98 (d, J=5.0 Hz, 1H), 7.18 (d, J=5.0 Hz, 1H), 6.98 (s, 1H), 0.99 (s, 9H), 0.87 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 156.0 (Cq), 141.9 (CH), 125.2 (Cq), 121.7 (Cq), 119.5 (CH), 117.3 (CH), 84.6 (Cq), 29.7 (3CH.sub.3), 27.1 (Cq), 0.7 (2CH.sub.3). HRMS (+ESI) calculated for C.sub.13H.sub.18BrIN.sub.2Si (M+H+): 436.9540 found: 436.9538.

Synthesis of 4-((4-bromo-1-(tert-butyldimethylsilyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethylaniline 207

(561) The compound was prepared according to procedure C2 and purified by flash column chromatography on silicagel (dichloromethane/petroleum ether=20/80). yellowish amorphous solid (54%), Rf=0.5 (ethyl acetate/petroleum ether=20/80). mp: 120-122 C. IR (, cm.sup.1, neat) 2952, 2890, 2851, 1603, 1568, 1538, 1507, 1489, 1443, 1431, 1403, 1374, 1338, 1324, 1293, 1246, 1229, 1191, 1157, 1120, 1104, 1071, 1046, 980, 942, 907. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 8.02 (d, J=5.2 Hz, 1H), 7.46 (d, J=8.9 Hz, 2H), 7.17 (d, J=5.2 Hz, 2H), 6.84 (s, 1H), 6.66 (d, J=8.9 Hz, 2H), 2.99 (s, 6H), 0.95 (s, 9H), 0.79 (s, 6H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 154.2 (Cq), 150.4 (Cq), 143.0 (CH), 132.4 (2CH), 127.2 (Cq), 123.6 (Cq), 123.1 (Cq), 119.5 (CH), 111.9 (2CH), 110.3 (CH), 109.3 (Cq), 96.8 (Cq), 82.3 (Cq), 40.2 (2CH.sub.3), 26.8 (3CH.sub.3), 19.9 (Cq), 1.5 (3CH.sub.3). HRMS (+ESI) calculated for C.sub.2H.sub.28BrN.sub.3Si (M+H+): 454.1308, found: 454.1309.

Example 71.5 Synthesis of N,N-dimethyl-4-((4-((4-(4,5,5-tetramethylcm-1,32-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)aniline 202

(562) ##STR00401##

(563) Under argon, 4-((4-bromo-1-(tert-butyldimethylsilyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)-N,N-dimethyl aniline 207 (100 mg, 0.22 mmol, 1.0 eq.) was dissolved in dioxane (1 ml) followed by addition of bis(pinacolato)diboron (1 12 mg, 0.44 mmol, 2.0 eq.) and KOAc (64 mg, 0.66 mmol, 3.0 eq.). Then, the reaction medium is degassed for 10 minutes before adding Pd(dppf).sub.2Cl.sub.2.dcm (18 mg, 0.022 mmol, 0.1 eq.). The reaction mixture was heated at 100 C. for 4 h. After cooling, the solvent was evaporated under reduced pressure. Finally, the crude is purified by flash column chromatography on silicagel eluting with (dichloromethane/petroleum ether=20/80) to yield the intermediate but with 10% of bis (pinacolato) diboron). Then, the crude is dissolved in 5 ml of THF. At 0 C., a solution of TBAF in THF (C=1 M, 0.09 ml, 0.09 mmol, 1.2 eq.) was added dropwise. After 1 h at 0 C., 10 ml of water and 10 ml of ethyl acetate are successively added. The organic phases are extracted 3 times with ethyl acetate (30 ml). Together, they are dried with MgSO.sub.4, filtered through cotton and evaporated under reduced pressure. The crude was purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=20/80) to yield compound 199 (20 mg, 24% over 2 steps) as a solid yellow. Rf=0.1 (ethyl acetate/petroleum ether=10/90). mp>260 C. IR (v, cm.sup.1, neat) 3291, 2962, 2930, 2853, 2102, 1606, 1511, 1463, 1434, 1373, 1356, 1336, 1273, 1245, 1227, 1185, 1141, 1093, 1023, 935. .sup.1H NMR (250 MHz, DMSO-d.sub.6, 20 C.) 12.06 (s, 1H), 8.21 (m, 1H), 7.33 (m, 3H), 6.84 (s, 1H), 6.71 (d, J=8.7 Hz, 2H), 2.93 (s, 6H), 1.31 (s, 12H). .sup.13C NMR (63 MHz, DMSO-d.sub.6, 20 C.) 150.7 (Cq), 148.4 (2Cq), 143.5 (CH), 132.9 (2CH), 124.4 (Cq), 122.2 (CH), 121.4 (Cq), 112.4 (2CH), 107.9 (Cq), 107.0 (CH), 95.6 (Cq), 84.4 (Cq), 80.5 (2Cq), 40.7 (2CH.sub.3), 25.2 (4CH.sub.3). HRMS (+ESI) calculated for C.sub.23H.sub.26BN.sub.3O.sub.2 (M+H+): 388.2190, found 388.2193.

Example 72: 5-Fluoro-2-((5-(methoxymethyl)furan-2-yl)ethynyl)-1H-pyrrolo[2,3-b] pyridine 215

(564) ##STR00402##

(565) 5-Fluoro-2-((5-(methoxymethyl)furan-2-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 215 was synthesized in two steps by methylation reaction of true alkyne 212 followed by a Sonogashira reaction from the halogenoazaindole

(566) ##STR00403##

Example 72.1 Synthesis of 2-ethynyl-5-(methoxymethyl)furane 213

(567) Compound 213 was prepared according to procedure M from 212 and isolated as a brown oil (90%). Rf=0.25 (petroleum ether/ethyl acetate=9/1). IR (v, cm.sup.1, neat) 3517, 3165, 2896, 2179, 1654, 1560, 1370, 1111, 957, 770. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 6.58 (m, 1H), 6.45-6.28 (d, J 0.6 Hz, 1H), 4.35 (d, J 0.6 Hz, 2H), 3.36 (s, 3H), 3.23 (s, 1H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 170.4 (Cq), 129.8 (CH), 114.6 (CH.sub.2), 109.4 (Cq), 102.1 (CH), 78.9 (CH), 76.8 (Cq), 61.3 (CH.sub.3). HRMS (+ESI) calculated for C.sub.14H.sub.9FN.sub.2O.sub.2 (M+H.sup.+): 137,1738 found: 137,1278.

Example 72.2 Synthesis of 5-Fluoro-2-((5-(methoxymethyl)furan-2-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 215

(568) Compound 215 was synthesized according to procedure C2 and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=1/9). The compound was obtained as a yellow solid (35%). mp: 162-164 C. Rf=0.31 (ethyl acetate/petroleum ether=1/9). IR (v, cm.sup.1, neat) 3117, 3059, 2981, 2890, 2727, 1584, 1505, 1433, 1374, 1360, 1346, 1297, 1251, 1179, 1157, 1087, 1020, 981, 935, 963, 876, 855, 758, 628. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.43 (s, 1H), 8.26 (m, 1H), 7.83 (m, 1H), 6.97-6.85 (m, 2H), 6.56 (m, 1H), 4.35 (s, 2H), 3.23 (s, 3H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 154.7 (Cq), 145.7 (Cq), 135.5 (Cq), 133.6 (CH), 120.7 (Cq), 119.7 (d, J=47.8 Hz, CH), 117.57 (Cq), 114.5 (d, J=23.6 Hz, CH), 114.2 (Cq), 111.6 (CH), 107.6 (CH), 86.3 (Cq), 83.8 (Cq), 65.7 (CH.sub.2), 58.4 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 138.1 (m, 1F).

(569) HRMS (+ESI) calculated for C.sub.14H.sub.9FN.sub.2O.sub.2 (M+H.sup.+): 271,087732, found: 271,087812.

Example 73: 5-(2-(5-Fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)furan-2-yl)methanol 221

(570) ##STR00404##

(571) 5-(2-(5-Fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)ethynyl)furan-2-yl)methanol 221 was synthesized in one step by Sonogashira reaction from true alkyne

(572) ##STR00405##

(573) Compound 221 was prepared according to procedure C2 and purified by flash column chromatography on silicagel (methanol/dichloromethane/ammonia=4/94/2). The compound was obtained as a yellow solid (30%). mp: 240-242 C. Rf=0.42 (methanol/dichloromethane/ammonia=4/94/2) IR (v, cm.sup.1, neat) 3136, 2220, 2186, 2021, 1993, 1966, 1589, 1504, 1408, 1300, 1237, 1208, 1142, 1008, 985, 870, 800, 768, 611. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.38 (s, 1H), 8.28 (d, J=2.2 Hz, 1H), 7.85 (m, 1H), 7.35 (m, 1H), 6.98 (d, J=2.2 Hz, 1H), 6.84 (d, J=2.2 Hz, 1H), 4.71-4.52 (m, 2H), 3.17 (m, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 151.1 (Cq), 145.6 (Cq), 133.7 (Cq), 133.4 (m, J=29.3 Hz, 2CH), 124.8 (CH), 121.3 (Cq), 119.7 (Cq), 114.1 (d, J=20.6 Hz, CH), 106.9 (d, J=4.5 Hz, CH), 87.4 (Cq), 85.4 (Cq), 58.8 (CH.sub.2), 31.1 (Cq). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 138.3 (m, 1F). HRMS (+ESI) calcule pour C.sub.14H.sub.9FN.sub.2O.sub.2 (M+H+): 273,0492 trouve: 273,0489.

Example 74: 5-Fluoro-2-((5-(methoxymethyl)furan-2-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 222

(574) ##STR00406##

(575) 5-Fluoro-2-((5-(methoxymethyl)furan-2-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 222 was synthesized in 2 steps by an methylation reaction of the primary alcohol followed by a Sonogashira reaction starting rom the true alkyne and corresponding halogenated azaindole

(576) ##STR00407##

Example 74.1 Synthesis of 2-Ethynyl-5-(methoxymethyl)thiophene 220

(577) Compound 220 was prepared according to procedure M as a brown oil (90%). Rf=0.25 (petroleum ether/ethyl acetate=9/1). IR (v, cm.sup.1, neat) 3400, 3250, 2980, 2052, 1620, 1433, 1269, 1087, 922, 831. .sup.1H NMR (250 MHz, CDCl.sub.3, 20 C.) 7.16-7.05 (m, 1H), 6.84-6.74 (m, 1H), 4.58-4.45 (m, 2H), 3.35 (s, 3H), 3.30 (s, 1H). .sup.13C NMR (63 MHz, CDCl.sub.3, 20 C.) 167.1 (Cq), 131.9 (CH), 117.1 (CH.sub.2), 108.2 (Cq), 103.8 (CH), 79.1 (CH), 77.1 (Cq), 60.2 (CH.sub.3). HRMS (+ESI) calculated for C.sub.14H.sub.9FN.sub.2O.sub.2 (M+H.sup.+): 153,08976 found: 153,09459.

Example 74.2 Synthesis of 5-Fluoro-2-((5-(methoxymethyl)thiophen-2-yl)ethynyl)-1H-pyrrolo[2,3-b]pyridine 222

(578) Compound 222 was synthesized according to procedure C2 and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=1/9). The compound was obtained as a yellow solid (35%). mp: 154-156 C. Rf=0.31 (ethyl acetate/petroleum ether=1/9). IR (v, cm.sup.1, neat) 3114, 3047, 2929, 2855, 2203, 1587, 1523, 1503, 1471, 1427, 1394, 1375, 1295, 1242, 1219, 1175, 1142, 1087, 1007, 980, 950, 799, 769, 643, 566. .sup.1H NMR (400 MHz, CDCl.sub.3, 20 C.) 10.95 (s, 1H), 8.29 (s, 1H), 7.64 (m, 1H), 7.32-7.19 (m, 2H), 6.96 (m, 1H), 6.76 (s, 1H), 4.64 (s, 3H), 3.44 (s, 4H). .sup.13C NMR (101 MHz, CDCl.sub.3, 20 C.) 157.1 (Cq), 154.6 (Cq), 145.1 (Cq), 144.3 (Cq), 132.8 (Cq), 132.6 (d, J 16.2 Hz, CH), 126.3 (CH), 121.8 (d, J 47.8 Hz, CH), 120.6 (Cq), 114.4 (d, J 20.9 Hz, CH), 106.5 (d, J 4.5 Hz, CH), 87.4 (Cq), 84.8 (Cq), 69.1 (CH.sub.2), 58.1 (CH.sub.3). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 137.3 (m, 1F). HRMS (+ESI) calcule pour C.sub.14H.sub.9FN.sub.2O.sub.2 (M+H.sup.+): 287,06488 trouve: 287,06469

Example 75: 4-({[4-(2-{5-Fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl}ethynyl)phenyl]methoxy}methyl)piperidine 223

(579) ##STR00408##

(580) 4-({[4-(2-{5-Fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl}ethynyl)phenyl] methoxy}methyl)piperidine 22 was synthesized in one step by a Sonogashira reaction departing from the true alkyne and corresponding halogenated azaindole

(581) ##STR00409##

(582) Compound 223 was synthesized according to procedure C2 from 4-{[(4-ethynylphenyl)methoxy]methyl}pyridine and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=3/7). The compound was obtained as a yellow solid (54%). mp:>260 C. Rf=0.29 (ethyl acetate/petroleum ether=3/7). IR (v, cm.sup.1, neat) 2678, 1610, 1535, 1497, 1397, 1296, 1150, 1085, 1028, 880, 808, 760, 737, 591, 563. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.40 (s1, 1H), 8.60 (s, 2H), 8.28 (m, 1H), 7.86 (m, 1H), 7.60 (d, J=7.8 Hz, 2H), 7.49 (d, J=7.8 Hz, 2H), 7.40 (s1, 2H), 6.84 (d, J 2.0 Hz, 1H), 4.64 (2 s, 4H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 156.8 (Cq), 154.34 (Cq), 150.1 (Cq), 147.7 (Cq), 145.6 (Cq), 139.9 (Cq), 133.4 (CH), 133.13 (CH), 131.8 (2CH), 128.3 (2CH), 121.6 (CH), 120.78 (CH), 120.1 (d, J 7.5 Hz, Cq), 114.3 (CH), 114.1 (CH), 106.7 (d, J 4.6 Hz, CH), 93.6 (Cq), 82.2 (Cq), 71.8 (CH.sub.2), 70.4 (CH.sub.2).sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 137.8 (m, 1F). HRMS (+ESI) calculated for C.sub.14H.sub.9FN.sub.2O.sub.2 (M+H.sup.+): 258,135027, found: 258.135169.

Example 76: 2-[2-(4-Fluorophenyl)ethynyl]-1H-pyrrolo[2,3-b]pyridine 224

(583) ##STR00410##

(584) 2-[2-(4-Fluorophenyl)ethynyl]-1H-pyrrolo[2,3-b]pyridine 224 was synthesized in one step by a Sonogashira reaction departing from the true alkyne

(585) ##STR00411##

(586) Compound 224 was synthesized according to procedure C2 from 1-ethynyl-4-fluoro-benzene and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=3/7). The compound was obtained as a yellow solid (81%). mp:>260 C. Rf=0.29 (ethyl acetate/petroleum ether=3/7). IR (v, cm.sup.1, neat) 3117, 3056, 2979, 2877, 2817, 2703, 1536, 1397, 1359, 1228, 1197, 1155, 1020, 979, 935, 918, 833, 760, 652, 597. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.23 (s, 1H), 8.29 (dd, J 4.6, 1.6 Hz, 1H), 7.97 (dd, J 7.9, 1.6 Hz, 1H), 7.71-7.61 (m, 2H), 7.37-7.27 (m, 2H), 7.11 (dd, J 7.9, 4.6 Hz, 1H), 6.83 (d, J 1.6 Hz, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 6 163.9 (Cq), 161.4 (Cq), 148.8 (CH), 144.9 (CH), 134.1 (d, J=8.7 Hz, CH), 128.9 (CH), 119.9 (Cq), 119.2 (Cq), 118.59 (d, J=3.4 Hz, CH), 116.87 (d, J=5.9 Hz, CH), 116.6 (CH), 106.8 (CH), 99.9 (Cq), 92.1 (Cq), 82.4 (Cq). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 109.7 (m, 1F). HRMS (+ESI) calculated for C.sub.14H.sub.9FN.sub.2O.sub.2 (M+H.sup.+): 237,082253, for 237,082117.

Example 77: 2-((1H-Indol-4-yl)ethynyl)-5-fluoro-1H-pyrrolo[2,3-b]pyridine 225

(587) ##STR00412##

(588) 2-((1H-Indol-4-yl)ethynyl)-5-fluoro-1H-pyrrolo[2,3-b]pyridine 225 was synthesized in one step by a Sonogashira reaction of true alkyne

(589) ##STR00413##

(590) Compound 225 was synthesized according to procedure A from 4-ethynyl-1H-indole and purified by flash column chromatography on silicagel (ethyl acetate/petroleum ether=3/7). The compound was obtained as a yellow solid (15%). mp:>260 C. Rf=0.29 (ethyl acetate/petroleum ether=3/7 IR (v, cm.sup.1, neat) 3400, 3111, 3054, 2980, 2792, 2205, 1732, 1607, 1582, 1531, 1499, 1462, 1416, 1394, 1344, 1310, 1259, 1227, 1196, 1138, 1099, 1066, 985, 887, 803, 726, 604, 556. .sup.1H NMR (400 MHz, DMSO-d.sub.6, 20 C.) 12.30 (s1, 1H), 11.38 (s1, 1H), 8.25 (s, 1H), 7.83 (dt, J=6.5 Hz, 2H), 7.46 (dd, J=6.5 Hz, 2H), 7.30 (d, J=1.6 Hz, 1H), 6.77 (d, J=1.6 Hz, 1H), 6.53-6.48 (m, 1H). .sup.13C NMR (101 MHz, DMSO-d.sub.6, 20 C.) 145.6 (Cq), 136.4 (Cq), 132.6 (CH), 132.4 (CH), 128.1 (Cq), 127.4 (CH), 124.76 (CH), 124.33 (CH), 122.7 (Cq), 120.34 (Cq), 113.8 (d, J=20.9 Hz, CH), 112.5 (Cq), 111.8 (CH), 105.8 (CH), 102.1 (CH), 96.1 (Cq), 79.5 (Cq). .sup.19F NMR (376 MHz, DMSO-d.sub.6, 20 C.) 138.7 (m, 1F). HRMS (+ESI) calculated for C.sub.14H.sub.9FN.sub.2O.sub.2 (M+H.sup.+): 276,093152, found 276,093345.

Compounds for using in imaging and particularly for the diagnosis of neurodegenerative diseases

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A61K51/0455

HUMAN NECESSITIES

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C07D471/04

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C07D471/04

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