Substituted imidazolium sulfuranes and their use

Abstract

The present invention refers to substituted imidazolium sulfuranes, the use thereof for the transfer of a CN group or an alkyne group.

Claims

1. An imidazolium sulfurane of the formula (I): ##STR00007## wherein: R.sup.1 and R.sup.2 each independently represent hydrogen, alkyl, aralkyl, aryl, heteroaryl, each being optionally substituted by one or more hetero atoms selected from O, N, S or halogen, or R.sup.1 and R.sup.2 may together form a hydrocarbon ring structure, optionally substituted by one or more hetero atoms selected from O, N, S and halogen; R.sup.3 and R.sup.4 each independently represent a lower alkyl group having 1 to 6 carbon atoms, each lower alkyl group being optionally substituted by one or more hetero atoms selected from O, N, S or halogen; X is an anion selected from halogen or a non- or weak-coordinating anion; Y represents a group of the CW formula wherein W represents N, CR.sup.5, ##STR00008## or CCO.sub.2R.sup.5 wherein R.sup.5 is selected from the group consisting of C.sub.1 to C.sub.20 straight chain, branched chain or cyclic aliphatic hydrocarbons, optionally having one or more unsaturated bonds or C.sub.6 to C.sub.20 aromatic hydrocarbons and partially arene-hydrogenated hydrocarbons, each hydrocarbon optionally being substituted by one or more hetero atoms selected from O, N, S, halogen or a silylgroup; with the proviso that compounds of the formula (I) wherein R.sup.1 and R.sup.2 are hydrogen, R.sup.3 and R.sup.4 are methyl, X is halogen and Y is CN are excluded.

2. The imidazolium sulfurane of the formula (I) as claimed in claim 1 wherein: R.sup.1 and R.sup.2 each independently represent hydrogen or lower alkyl having 1 to 6 carbon atoms, optionally substituted by one or more hetero atoms selected from O, N, S or halogen, or R.sup.1 and R.sup.2 may together form a 5 to 7 membered hydrocarbon ring structure, optionally substituted by one or more hetero atoms selected from O, N, S or halogen; R.sup.3 and R.sup.4 each independently represent a lower alkyl group having 1 to 6 carbon atoms, each lower alkyl group being optionally substituted by one or more hetero atoms selected from O, N, S or halogen; X is an anion selected from halogen or a non- or weak-coordinating anion; Y represents a group of the formula CW wherein W represents N, CR.sup.5 or CCO.sub.2R.sup.5 wherein R.sup.5 is selected from the group consisting of C.sub.1 to C.sub.20 straight chain, branched chain or cyclic aliphatic hydrocarbons, C.sub.3-C.sub.8-heterocycloalkyl or C.sub.6 to C.sub.20 aromatic hydrocarbons and partially arene-hydrogenated forms, each hydrocarbon optionally being substituted by one or more hetero atoms selected from O, N, S, halogen or a tri-lower alkyl-silygroup.

3. The imidazolium sulfurane of the formula (I) as claimed in claim 1, wherein: R.sup.1 and R.sup.2 each independently represent hydrogen or lower alkyl having 1 to 6 carbon atoms, optionally substituted by one or more oxygen atoms, or R.sup.1 and R.sup.2 may together form a 5 to 7 membered hydrocarbon ring structure, optionally substituted by one or more oxygen or nitrogen atoms; R.sup.3 and R.sup.4 each independently represent a lower alkyl group selected from methyl, ethyl, propyl, iso-propyl; X is an anion selected from halogen or a non- or weak-coordinating anion; Y represents a group of the CW formula wherein W represents N, CR.sup.5 or CCO.sub.2R.sup.5 wherein R.sup.5 is selected from the group consisting of C.sub.1 to C.sub.20 straight chain, branched chain or cyclic aliphatic hydrocarbons, optionally having one or more unsaturated bonds or C.sub.6 to C.sub.20 aromatic hydrocarbons and partially arene-hydrogenated forms, each hydrocarbon optionally being substituted by one or more hetero atoms selected from O, N, S or halogen a tri-lower alkyl-silygroup.

4. The imidazolium sulfurane of the formula (I) as claimed in claim 1, wherein: R.sup.1 and R.sup.2, R.sup.3 and R.sup.4 and X have the meaning as given in claim 1 and Y represents a group of the formula: ##STR00009## wherein R.sup.5 may be the same or different and may be selected from the group consisting of C.sub.1 to C.sub.20 straight chain, branched chain or cyclic aliphatic hydrocarbons, optionally having one or more unsaturated bonds or C.sub.6 to C.sub.20 aromatic hydrocarbons and partially arene-hydrogenated hydrocarbons, each hydrocarbon optionally being substituted by one or more hetero atoms selected from O, N, S or halogen a tri-lower alkyl-silygroup.

5. Process for preparing an imidazolium sulfurane compound of the formula (I): ##STR00010## wherein R.sup.1 and R.sup.2, R.sup.3 and R.sup.4, X and Y have the meanings as given in claim 1, said process comprising reacting a compound of the formula (II): ##STR00011## wherein R.sup.1 to R.sup.4 have the meaning as given in claim 1, in a first step, with a halogen to yield a resulting compound, and the resulting compound is reacted in a second step with a compound of the formula RCW, wherein R is a lower alkyl silyl group, wherein the lower alkyl has 1 to 6 carbon atoms.

6. Process comprising reacting a compound of the formula (I): ##STR00012## wherein R.sup.1 and R.sup.2 each independently represent hydrogen, alkyl, aralkyl, aryl, heteroaryl, each being optionally substituted by one or more hetero atoms selected from O, N, S or halogen, or R.sup.1 and R.sup.2 may together form a hydrocarbon ring structure, optionally substituted by one or more hetero atoms selected from O, N, S and halogen; R.sup.3 and R.sup.4 each independently represent a lower alkyl group having 1 to 6 carbon atoms, each lower alkyl group being optionally substituted by one or more hetero atoms selected from O, N, S or halogen; X is an anion selected from halogen or a non- or weak-coordinating anion; Y represents a group of the CW formula wherein W represents N, CR.sup.5, ##STR00013## or CCO.sub.2R.sup.5 wherein R.sup.5 is selected from the group consisting of C.sub.1 to C.sub.20 straight chain, branched chain or cyclic aliphatic hydrocarbons, optionally having one or more unsaturated bonds or C.sup.6 to C.sup.20 aromatic hydrocarbons and partially arene-hydrogenated hydrocarbons, each hydrocarbon optionally being substituted by one or more hetero atoms selected from O, N, S, halogen or a silylgroup; with an organic nucleophilic compound R.sup.NH wherein R.sup.N is alkyl, aralkyl, aryl or heteroaryl, each being optionally substituted by one or more hetero atoms selected from O, N, and S, in an organic solvent, and optionally in the presence of a Lewis acid catalyst, resulting in a transfer of the group Y in order to yield a compound of the formula R.sup.NY.

7. Process according to claim 6, wherein Y represents CN, and said reacting is conducted for a direct electrophilic cyanation of a CH bond in an organic compound.

8. Process according to claim 6, wherein W represents CR.sup.5 or CCO.sub.2R.sup.5, and said reacting is conducted for a direct electrophilic alkynylation of a CH bond in an organic compound.

9. An imidazolium sulfurane of the formula (I): ##STR00014## wherein: R.sup.1 and R.sup.2 each independently represent alkyl, aralkyl, aryl, heteroaryl, each being optionally substituted by one or more hetero atoms selected from O, N, S or halogen, or R.sup.1 and R.sup.2 may together form a hydrocarbon ring structure, optionally substituted by one or more hetero atoms selected from O, N, S and halogen; R.sup.3 and R.sup.4 each independently represent a lower alkyl group having 1 to 6 carbon atoms, each lower alkyl group being optionally substituted by one or more hetero atoms selected from O, N, S or halogen; X is an anion selected from halogen or a non- or weak-coordinating anion; Y represents a group of the CW formula wherein W represents N, CR.sup.5, ##STR00015## or CCO.sub.2R.sup.5 wherein R.sup.5 is selected from the group consisting of C.sub.1 to C.sub.20 straight chain, branched chain or cyclic aliphatic hydrocarbons, optionally having one or more unsaturated bonds or C.sub.6 to C.sub.20 aromatic hydrocarbons and partially arene-hydrogenated hydrocarbons, each hydrocarbon optionally being substituted by one or more hetero atoms selected from O, N, S, halogen or a silylgroup.

10. The imidazolium sulfurane of the formula (I) as claimed in claim 9, wherein R.sup.1 and R.sup.2 each independently represent alkyl.

11. Process according to claim 5, wherein RCW is trimethylsilyl cyanide.

12. An imidazolium sulfurane of the formula (I): ##STR00016## wherein: R.sup.1 and R.sup.2 each independently represent hydrogen, alkyl, aralkyl, aryl, heteroaryl, each being optionally substituted by one or more hetero atoms selected from O, N, S or halogen, or R.sup.1 and R.sup.2 may together form a hydrocarbon ring structure, optionally substituted by one or more hetero atoms selected from O, N, S and halogen; R.sup.3 and R.sup.4 each independently represent a lower alkyl group having 2 to 6 carbon atoms, each lower alkyl group being optionally substituted by one or more hetero atoms selected from O, N, S or halogen; X is an anion selected from halogen or a non- or weak-coordinating anion; Y represents a group of the CW formula wherein W represents N, CR.sup.5, ##STR00017## or CCO.sub.2R.sup.5 wherein R.sup.5 is selected from the group consisting of C.sub.1 to C.sub.20 straight chain, branched chain or cyclic aliphatic hydrocarbons, optionally having one or more unsaturated bonds or C.sub.6 to C.sub.20 aromatic hydrocarbons and partially arene-hydrogenated hydrocarbons, each hydrocarbon optionally being substituted by one or more hetero atoms selected from O, N, S, halogen or a silylgroup.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The invention is further illustrated by the attached Drawings. In said Drawings:

(2) FIG. 1 contains Scheme 1, which illustrates the use of imidazolium-substituted sulfuranes for the synthesis of 2-thiocyanoimidazolium salts;

(3) FIG. 2 contains Chart 1, which exemplifies the substrate scope of the electrophilic cyanation using 2-thiocyanoimidazolium salts;

(4) FIG. 3 contains Scheme 2, which illustrates the synthesis of 2-imidazolium thioalkynes; and

(5) FIG. 4 contains Chart 2, which exemplifies the substrate scope of the electrophilic alkynylation using a specific 2-imidazolium thioalkyne.

(6) As illustrated in Scheme 1, the inventors submitted thioureas 1 and 2 to already described halogenation conditions, and obtained the corresponding hypervalent sulfur compounds 3-5 as bright yellow to orange solids in high yields and analytic purity (Scheme 1). Subsequent addition of one equivalent of Me.sub.3SiCN caused the immediate disappearance of the color and formation of the desired imidazolium thiocyanates 6-8. Compounds 6-8 were isolated as air stable pale yellow solids in excellent yields, and can be stored at room temperature for months without evident decomposition. This synthetic route towards 6-8 could be scaled to multigram quantities.

(7) Once prepared, the ability of these species to transfer the CN group to organic nucleophiles was evaluated by the inventors.

(8) The inventors started their survey by studying the reaction of 8 with simple commercially available amines, and they found that the employment of DIPEA as base in dichloromethane efficiently promoted the N-cyanation to afford the desired cyanamides 10-13 in good isolated yields and short reaction times (Chart 1). The presence of alcohol substituents, as in the case of S-diphenylprolinol, does not seem to be detrimental for the process (13). The same protocol was also applicable to the cyanation of other substrates such as aromatic thiols, enolates, enamines and activated methylenes providing the corresponding aromatic thiocyanates 14-16, -amido or keto nitriles 17-22, and -cyano sulphones 23 in good to excellent yields. Note that for the preparation of 19 and 20, compound 6 was preferred to 8 as cyanating reagent since thiourea byproduct 1 is easier to separate than 2 from the title products.

(9) The direct cyanation of CH bonds in aromatic compounds has a tremendous interest since (hetero)aromatic nitriles are really valuable intermediates not only in synthetic and medicinal chemistry but also in material science. Therefore, the inventors focused their efforts on these more challenging compounds. At the outset, the inventors took N-methyl indole as model substrate. As shown in Chart 1, using the procedure already described (Method A), N-methyl indole was regioselectively cyanated at the C-3 position (24), albeit with moderate conversion. Assuming that additional activation of the cyanating reagent could be beneficial when less nucleophilic substrates were employed, the inventors pursued the same transformation in the presence of catalytic amounts of Lewis acids. In these assays the employment of 9 (with hexafluoroantimoniate counteranion) as cyanating reagent is mandatory since the presence of halide anions cancels any catalyst effect.

(10) After an extensive survey, the use of catalytic amounts of BF.sub.3.OEt.sub.3 (20 mol. %) was determined to be optimal to promote the cyanation of N-methyl indole in terms of isolated yield and reaction time, which was up to eight folds reduced (Chart 1, compound 24, Method B). Having found these new reaction conditions, the scope of the transformation was further explored. Gratifyingly, the range of additional substrates that could be also converted into the desired nitriles could be substantially expanded, including substituted pyrroles, electron rich benzene derivatives and polycyclic aromatics (Chart 1, compounds 24-33).

(11) To preliminarly elucidate some mechanistic aspects of this reaction, the inventors carried out the cyanation of N-methyl indole in the presence of typical radical inhibitors such as TEMPO or BHT (50 mol % each), finding no drop in the yield of the cyanated product. Moreover, the functionalization of N-methyl indole is completely selective at the C-3 position, and no oxidative coupling products were detected. Combined these results suggest an electrophilic substitution mechanism rather than a radical pathway for this process.

(12) The cyanation protocol established by the inventors distinguishes itself by operational simplicity, safeness and a broad reactivity profile if compared with alternative electrophilic cyanating reagents: Cyanogen bromide has a comparable substrate scope; however, its toxicity and low vapor pressure at room temperature warns off its use. On the other hand, cyanating reagents based on hypervalent iodine reagents show strong exothermic decompositions on heating and therefore, they must be handle with appropriate knowledge and safety measures. Analysis of 8 by differential scanning calorimetry (DSC) up to 200 C. did not detect any sharp exothermic decomposition signal.

(13) In an attempt to further evaluate the utility of the imidazolium sulfurane platform A for the design of additional electrophilic group-transfer reagents, and considering the analogue electronic structure between cyanides and alkynes decorated with electron withdrawing substituents, the inventors speculated that imidazolium thioalkynes such as 34 might also be suitable reagents for the electrophilic alkynylation of organic substrates. Hence, the inventors first set up to prepare salt 34 by reaction of 5 with lithiated ethyl propiolate; however, only complex reaction mixtures were obtained. Conversely, addition of the softer silver propiolate to solutions of 5 afforded the desired alkynylated imidazolium 34 as dibromoargentate salt. This primary product slowly decomposes in the presence of light. Hence, 34 was directly elaborated through anion exchange to 35, which is a slightly orange powder insensitive to light or air (Scheme 2).

(14) With 35 completely characterized, its potential as ethynylation reagent was preliminarily examined. In the presence of DIPEA, the alkynylation of aliphatic, electron rich, and electron poor aromatic thiols smoothly proceeded in excellent yields (Chart 2, 36-38). Activated amides and ketoesters also afforded the desired alkynylated products (Chart 2, 39 and 40); however, electron rich benzene derivatives or polycyclic aromatic compounds did not react with 35 even in the presence of catalytic BF.sub.3.OEt.sub.3 or stoichiometric amounts of Brnsted acids.

(15) Experimental Procedures and Characterizations

(16) General:

(17) All solvents were purified by distillation over the drying agents indicated. All reactions were carried out under Ar atmosphere unless other way stated. IR: Nicolet FT-7199 spectrometer, wavenumbers in cm-1. MS (EI): Finnigan MAT 8200 (70 eV), ESIMS: Finnigan MAT 95, accurate mass determinations: Bruker APEX III FT-MS (7 T magnet). NMR: Spectra were recorded on a Bruker AV 400 or DPX 300; 1H and 13C chemical shifts () are given in ppm relative to TMS, coupling constants (J) in Hz. The solvent signals were used as references and the chemical shifts converted to the TMS scale. All flash chromatography was performed on Merck 60 silica gel (40-63 m). Thin-layer chromatography (TLC) analysis was performed using Merck silica gel 60 F254 TLC plates and visualized by UV irradiation and/or ceric ammonium molybdate, KMnO4 or p-anysaldehyde dip. All commercially available compounds (Acros, ABCR, Alfa Aesar, Aldrich) were used as received. Compounds 1, 2 and 4 were synthesized following the procedure described in literature; spectroscopic data are in agreement with those reported.

(18) Compound 1

(19) 1H NMR (400 MHz, CDCl3, ppm) =1.98 (6H, s), 3.42 (6H, s). 13C NMR (101 MHz, CDCl3, ppm) =9.1, 31.8, 120.7, 159.9. IR (neat, cm-1)=854, 1099, 1175, 1219, 1378, 1427, 1463, 1657, 2942.

(20) Compound 2

(21) 1H NMR (400 MHz, CDCl3, ppm) =1.42 (12H, d, J=7.3 Hz), 2.16 (6H, s), 5.17-6.22 (2H, br s). 13C NMR (101 MHz, CDCl3, ppm) =10.5, 20.9, 49.5, 121.5, 159.8. IR (neat, cm-1)=906, 980, 1025, 1089, 1105, 1138, 1206, 1338, 1368, 1412, 1464, 1643, 2937, 2974. HRMS: calcd. for C11H21N2S [M+]=213.1419; found=213.1419.

(22) Compound 3

(23) Bromine (655 L, 12.81 mmol) was added at 0 C. to a solution of compound 1 (2.00 g, 12.81 mmol) in dry DCM (21 mL), and the reaction slowly warmed up to RT during 3 hours. After removal of all volatiles under vacuum, compound 3 was obtained as an orange solid (3.88 g, 97%). 1H NMR (300 MHz, CDCl3, ppm) =2.27 (6H, s), 3.81 (6H, s). 13C NMR (75 MHz, CDCl3, ppm) =9.7, 33.8, 127.8. IR (neat, cm-1)=783, 855, 1032, 1230, 1372, 1429, 1490, 1624, 2944. HRMS: calcd. for C7H12N2BrS [M-Br]=234.9898; found=234.9899.

(24) Compound 4

(25) Following the procedure described in the literature, SO2Cl2 (517 L, 5.18 mmol) was added to a solution of compound 2 (1.00 g, 4.71 mmol) in 20 mL of toluene at 0 C. The reaction mixture was left to warm up to RT for 1 hour. The precipitate was filtered off, washed with cold toluene and dried under vacuum to afford compound 4 as a yellowish solid (979 mg, 74%). 1H NMR (300 MHz, CDCl3, ppm) =1.67 (12H, d, J=7.1 Hz), 2.37 (6H, s), 5.69 (2H, hept, J=7.1 Hz). 13C NMR (75 MHz, CDCl3, ppm) =10.5, 21.0, 53.5, 127.8, 147.6. IR (neat, cm-1)=978, 1032, 1110, 1137, 1215, 1369, 1420, 1610, 2878, 2935. HRMS: calcd. for C11H20N2CIS [M]=247.1030; found=247.1030.

(26) Compound 5

(27) To a solution of compound 2 (20.13 g, 94.77 mmol) in dry DCM (100 mL) was added bromine (4.9 mL, 94.77 mmol) at 0 C. and the reaction was left to warm up to RT for 3 hours. After removal of all volatiles under vacuum, compound 5 was obtained as an orange solid (33.05 g, 95%). 1H NMR (300 MHz, CDCl3, ppm) =1.68 (12H, d, J=7.1 Hz), 2.37 (6H, s), 5.67 (2H, hept, J=7.1 Hz). 13C NMR (75 MHz, CDCl3, ppm) =10.7, 20.6, 53.7, 128.3, 146.0. IR (neat, cm-1)=907, 980, 1028, 1112, 1137, 1217, 1371, 1423, 1606, 2877, 2936, 2972. HRMS: calcd. for C11H20BrN2S [M]=291.0523; found=291.0525.

(28) Compound 6

(29) Trimethylsilyl cyanide (252 L, 2 mmol) was added at room temperature to a solution of 3 (632 mg, 2 mmol) in dry DCM (5 mL). After stirring for 30 minutes all the volatiles were removed under vacuum and the obtained solid washed with dry ether to afford 6 as a white solid (501 mg, 96%). 1H NMR (400 MHz, CDCl3, ppm) =2.35 (6H, s), 3.96 (6H, s). 13C NMR (101 MHz, CDCl3, ppm) =9.9, 34.7, 106.6, 130.3, 131.8. IR (neat, cm-1)=774, 860, 1032, 1102, 1232, 1374, 1439, 1508, 1631, 2168, 2930, 2969. HRMS: calcd. for C8H12N3S [M-Br]=182.0748; found=182.0746.

(30) Compound 7

(31) TMSCN (252 L, 2 mmol) was added dropwise to a solution of 4 (454 mg, 2 mmol) in dry DCM (5 mL) at 0 C., and the reaction mixture stirred at room temperature for 1 hour. After that the solvent was evaporated and the remaining solid washed twice with diethyl ether and dried under vacuum to afford compound 7 as an off-white solid (409 mg, 94%). 1H NMR (400 MHz, CDCl3, ppm) =1.72 (12H, d, J=6.9 Hz), 2.40 (6H, s), 5.40 (2H, hept, J=7.1 Hz). 13C NMR (101 MHz, CDCl3, ppm) =10.1, 20.1, 54.0, 108.1, 129.3, 131.4. IR (neat, cm-1)=907, 980, 1114, 1140, 1216, 1342, 1371, 1393, 1457, 1607, 2151, 2938, 2971.

(32) HRMS: calcd. for C11H14N2 [M-Cl]=238.1373; found=238.1372.

(33) Compound 8

(34) TMSCN (5.60 mL, 45.16 mmol) was added dropwise at 0 C. to a solution of compound 5 (14.01 g, 37.64 mmol) in dry DCM (50 mL) and the reaction mixture was stirred at RT for 3 h. The solvent was then evaporated and the remaining solid washed twice with diethyl ether and dried under vacuum to afford compound 8 as a pale yellow solid (10.66 g, 89%). 1H NMR (300 MHz, CDCl3, ppm) =1.72 (12H, d, J=7.1 Hz), 2.40 (6H, s), 5.38, (2H, hept, J=7.1 Hz). 13C NMR (75 MHz, CDCl3, ppm) =10.9, 20.9, 55.0, 107.7, 130.4, 131.7. IR (neat, cm-1)=910, 1109, 1220, 1372, 1396, 1619, 2154, 2939, 3003, 3467. HRMS: calcd. for C12H20N3S [M]=238.1372; found=238.1372. Anal. Calcd for C12H20BrN3S: C, 45.29; H, 6.33; N, 13.20. Found: C, 45.55; H, 6.47; N, 12.99.

(35) Compound 9

(36) Solid AgSbF6 (4.34 g, 12.63 mmol) was added to a solution of 8 (4.02 g, 12.63 mmol) in dry MeCN (25 mL) and the reaction mixture was allowed to stir at RT for 1 h. The formed AgBr was then removed by filtration, affording 9 as a pale yellow solid (5.68 g, 95%). 1H NMR (400 MHz, CD3CN, ppm) =1.64 (12H, d, J=7.0 Hz), 2.40 (6H, s), 5.19 (2H, hept, J=6.9 Hz). 13C NMR (101 MHz, CD3CN, ppm) b=10.7, 20.9, 55.1, 106.8, 124.7, 133.7. IR (neat, cm-1)=905, 1114, 1139, 1217, 1381, 1397, 1460, 1600, 2173, 2999. 19F NMR (282 MHz, CD3CN) =124.05 (sext, JF-121Sb=1947 Hz). HRMS: calcd. for C12H20N3S1 [M-SbF6]=238.1373; found=238.1372. Anal. Calcd for C12H20F6N3SSb: C, 30.40; H, 4.25; N, 8.86.

(37) Found: C, 30.45; H, 4.21; N, 8.85.

(38) General Procedure for Electrophilic Cyanation of Amines and Thiols (Method A)

(39) To a solution of the desired substrate (0.30-0.38 mmol) and DIPEA (1.0 eq) in DCM (0.15 M), 8 (1.2 eq) was added and the reaction mixture stirred at room temperature for the specified time (see Chart 1). The reaction was quenched with saturated NH4Cl and extracted with DCM. The organic layers were dried over anhydrous Na2SO4, filtered, and the volatiles were removed under vacuum. The crude was purified by flash chromatography on silica gel (n-Hexane/EtOAc) affording the desired products.

(40) Compound 10

(41) Using the general procedure, compound 10 was prepared from 1-phenylpiperazine (45 L, 0.30 mmol), DIPEA (52 L, 0.30 mmol) and 8 (114 mg, 0.36 mmol), to obtain after flash chromatography (n-Hexane/EtOAc 7/3) a colorless oil (49 mg, 88%). 1H NMR (400 MHz, CDCl3, ppm) =3.18-3.27 (4H, m), 3.34-3.46 (4H, m), 6.88-6.99 (3H, m), 7.23-7.36 (2H, m). 13C NMR (101 MHz, CDCl3, ppm) =48.1, 48.3, 116.4, 116.8, 120.5, 128.6, 150.0. IR (neat, cm-1)=910, 998, 1139, 1173, 1229, 1266, 1326, 1380, 1448, 1494, 1597, 1721, 2209, 2822. HRMS: calcd. for C11H13N3Na1 [M+Na]=210.1001; found=210.1001.

(42) Compound 11

(43) Using the general procedure, compound 11 was prepared from N-isopropylbenzylamine (55 L, 0.33 mmol), DIPEA (57 L, 0.33 mmol) and 8 (124 mg, 0.39 mmol) to obtain after flash chromatography (n-Hexane/EtOAc 7/3) a colorless oil (52 mg, 92%). 1H NMR (400 MHz, CDCl3, ppm) =1.24 (3H, s), 1.26 (3H, s), 3.11 (1H, hept, J=6.5 Hz), 4.21 (2H, s), 7.30-7.42 (5H, m). 13C NMR (101 MHz, CDCl3, ppm) =19.7, 50.2, 53.5, 115.93, 127.5, 127.6, 128.1, 134.5. IR (neat, cm-1)=958, 1028, 1077, 1095, 1127, 1172, 1209, 1370, 1388, 1454, 1496, 1604, 2202, 2874, 2929, 2973, 3031. HRMS: calcd. for C11H14N2Na1 [M+Na]=197.1049; found=197.1049.

(44) Compound 12

(45) Using the general procedure, compound 12 was prepared from 4-tert-butylaniline (53 L, 0.34 mmol), DIPEA (59 L, 0.34 mmol) and 8 (129 mg, 0.40 mmol) to obtain after flash chromatography (n-Hexane/EtOAc 7/3) a white solid (47 mg, 79%). 1H NMR (400 MHz, CDCl3, ppm) =1.30 (9H, s), 5.99 (1H, s), 6.92-6.99 (2H, m), 7.32-7.40 (2H, dd, J=10.7, 5.4 Hz). 13C NMR (101 MHz, CDCl3, ppm) =30.6, 33.6, 110.4, 114.3, 125.9, 133.6, 146.1. IR (neat, cm-1)=1023, 1248, 1426, 1514, 1615, 2224, 2959, 3066, 3156. HRMS: calcd. for C11H14N2 [MH]=173.1084; found=173.1084.

(46) Compound 13

(47) Using the general procedure, compound 13 was prepared from (S)-()-,-diphenylprolinol (76 mg, 0.30 mmol), DIPEA (52 L, 0.30 mmol) and 8 (114 mg, 0.36 mmol) to obtain after flash chromatography (n-Hexane/EtOAc 7/3) a white solid (70 mg, 84%). 1H NMR (400 MHz, CDCl3, ppm) =1.70-1.87 (2H, m), 1.88-1.96 (2H, m), 2.60 (1H, s), 3.41-3.46 (1H, m), 4.81 (1H, t, J=6.9 Hz), 7.19-7.41 (6H, m), 7.43-7.49 (2H, m), 7.56-7.62 (2H, m). 13C NMR (101 MHz, CDCl3, ppm) =25.3, 28.2, 54.2, 69.3, 79.2, 117.4, 126.1, 127.2, 128.3, 143.6. IR (neat, cm-1)=961, 987, 1034, 1270, 1386, 1449, 1493, 1754, 2004, 2026, 2146, 2968, 3057, 3490. HRMS: calcd. for C18H19N2O1 [M+H]=279.1493; found=279.1491.

(48) Compound 14

(49) Using the general procedure, compound 14 was prepared from 2-mercaptobenzothiazole (63 mg, 0.38 mmol), DIPEA (66 L, 0.38 mmol) and 8 (145 mg, 0.45 mmol) to obtain after flash chromatography (n-Hexane/EtOAc 8/2) as yellow solid (66 mg, 91%). 1H NMR (400 MHz, CDCl3, ppm) =7.47 (1H, ddd, J=8.1, 7.3, 1.3 Hz), 7.54 (1H, ddd, J=8.3, 7.3, 1.3 Hz), 7.88 (1H, ddd, J=8.0, 1.2, 0.5 Hz), 8.00 (1H, brdd, J=8.2, 0.6 Hz). 13C NMR (101 MHz, CDCl3, ppm) =106.2, 120.6, 122.4, 125.6, 126.4, 135.7, 152.2, 152.6. IR (neat, cm-1)=1075, 1163, 1235, 1273, 1309, 1419, 1461, 1554, 1586, 1619, 1789, 1911, 1946, 2166, 2920, 2987, 3051. HRMS: calcd. for C8H4N2S2Na1 [M+Na]=214.9705; found=214.9708.

(50) Compound 15

(51) Using the general procedure, compound 15 was prepared from 4-nitrobenzenethiol (54 mg, 0.35 mmol), DIPEA (61 L, 0.35 mmol) and compound 8 (133 mg, 0.42 mmol) to obtain after flash chromatography (n-Hexane/EtOAc 8/2) a white solid (48 mg, 77%). 1H NMR (400 MHz, CDCl3, ppm) =7.63-7.72 (2H, m), 8.28-8.34 (2H, m). 13C NMR (101 MHz, CDCl3, ppm) =108.0, 125.1, 128.7, 133.3, 148.0. IR (neat, cm-1)=956, 1009, 1081, 1106, 1120, 1187, 1278, 1316, 1398, 1417, 1475, 1514, 1578, 1601, 1664, 1922, 2161, 2445, 2844, 3104. HRMS: calcd. for C7H4N2O2S1 [M]=179.9991; found=179.9993.

(52) Compound 16

(53) Using the general procedure, compound 16 was prepared from 1-naphthalenethiol (50 L, 0.36 mmol), DIPEA (62 L, 0.36 mmol) and 8 (136 mg, 0.43 mmol) to obtain after flash chromatography (n-Hexane/EtOAc 9/1) a pale yellow solid (56 mg, 85%). 1H NMR (400 MHz, CD2Cl2, ppm) =7.54 (1H, dd, J=8.3, 7.3 Hz), 7.64 (1H, ddd, J=8.2, 6.9, 1.2 Hz), 7.73 (1H, ddd, J=8.5, 7.0, 1.4 Hz), 7.93-7.99 (2H, m), 8.02 (1H, br d, J=8.0 Hz), 8.27 (1H, dd, J=8.5, 0.9 Hz). 13C NMR (101 MHz, CD2Cl2, ppm) =111.0, 121.1, 124.5, 126.3, 127.5, 128.4, 129.3, 131.9, 132.5, 133.0, 134.7. IR (neat, cm-1)=965, 1058, 1143, 1200, 1255, 1338, 1369, 1501, 1590, 1720, 1823, 1935, 2151, 2832, 3056. HRMS: calcd. C11H7N1S1 [M]=185.0298; found=185.0299.

(54) General Procedure for Electrophilic Cyanation of Activated Methylenes (Method A)

(55) DIPEA (1.0 eq.) was added to a solution of the desired substrate (0.30 mmol) in dry DCM (0.15 M). After stirring 30 min, solid 8 (1.2 eq.) was added and the reaction was allowed to stir for the specified time (see Chart 1). Quenched with HCl (1N) and extraction with EtOAc afforded a crude product that was purified by flash chromatography on silica gel (n-Hexane/EtOAc).

(56) Compound 17

(57) NaH (8 mg, 0.33 mmol) was added to a solution of 1,3-dimethylindolin-2-one (48 mg, 0.29 mmol.) in dry THF (2.0 mL) at 0 C. After stirring for 30 minutes, solid 8 (143 mg, 0.45 mmol) was added, and the reaction mixture was left to warm up to room temperature for 12 h. Quenching with HCl (1N) and extraction with EtOAc afforded a crude that was purified by flash chromatography on silica gel (n-Hexane/EtOAc 7/3). Compound 17 was obtained as a colorless solid (39 mg, 72%). 1H NMR (300 MHz, CDCl3, ppm) =1.67 (3H, s), 2.97 (3H, s), 6.61 (1H, d, J=7.4 Hz), 6.71 (1H, d, J=7.8 Hz), 6.86 (1H, td, J=7.4, 1.1 Hz), 7.20-7.28 (1H, m). 13C NMR (75 MHz, CDCl3, ppm) =17.5, 26.0, 51.8, 108.0, 121.7, 123.8, 128.6, 129.8, 131.3, 143.9, 177.8. IR (neat, cm-1)=758, 1027, 1093, 1156, 1263, 1303, 1346, 1373, 1453, 1473, 1607, 1697, 2935, 2967. HRMS: calcd. for C11H10N2ONa [M+Na]=209.0685; found 209.0685.

(58) Compound 18

(59) Using the general procedure, compound 18 was prepared from methyl 1-oxo-2,3-dihydro-1H-indene-2-carboxylate (57 mg, 0.30 mmol.), DIPEA (52 L, 0.30 mmol) and 8 (114 mg, 0.36 mmol). Purification by flash chromatography (n-Hexane/EtOAc 8/2) afforded a colorless oil (60 mg, 93%). 1H NMR (400 MHz, CDCl3, ppm) =3.71 (1H, d, J=17.3 Hz), 3.89 (3H, s), 3.96 (1H, d, J=17.3 Hz), 7.51 (1H, t, J=7.5 Hz), 7.56 (1H, dt, J=7.8, 0.9 Hz), 7.75 (1H, t, J=7.7 Hz), 7.86 (1H, m). HRMS: calcd. C12H9N1O3Na1 [M+Na]=238.0476; found=238.0474.

(60) Compound 19

(61) Using the general procedure, compound 19 was prepared from methyl 5-bromo-1-oxo-2,3-dihydro-1H-indene-2-carboxylate (81 mg, 0.30 mmol.), DIPEA (78 L, 0.45 mmol) and compound 6 (118 mg, 0.45 mmol) to obtain after flash chromatography (n-Hexane/EtOAc 7/3) a colorless oil (69 mg, 79%). 1H NMR (300 MHz, CDCl3, ppm) =3.65 (1H, d, J=17.4 Hz), 3.87 (3H, s), 3.91 (1H, d, J=17.4 Hz), 7.62 (1H, ddt, J=8.6, 1.6, 0.8 Hz), 7.69 (1H, dd, J=8.6, 0.8 Hz), 7.72 (1H, dd, J=1.6, 0.8 Hz). 13C NMR (75 MHz, CDCl3, ppm) =37.2, 54.4, 55.0, 115.4, 127.4, 130.0, 131.0, 133.0, 133.1, 152.9, 164.4, 189.5. IR (neat, cm-1)=958, 1018, 1092, 1236, 1308, 1329, 1445, 1490, 1651, 1720, 1741, 2252, 2890. HRMS: calcd. for C12H8NO3BrNa [M+Na]=315.9578; found=315.9579.

(62) Compound 20

(63) Using the general procedure, compound 20 was prepared from methyl 5-methoxy-1-oxo-2,3-dihydro-1H-indene-2-carboxylate3 (60 mg, 0.27 mmol), DIPEA (72 L, 0.41 mmol) and compound 8 (135 mg, 0.42 mmol) to obtain, after flash chromatography (n-Hexane/EtOAc 8/2) a colorless oil (39 mg, 59%). 1H NMR (300 MHz, CDCl3, ppm) =3.60 (1H, d, J=17.2 Hz), 3.83-3.93 (7H, m), 6.86-6.95 (1H, m), 6.99 (1H, dd, J=8.6, 2.2 Hz), 7.75 (1H, d, J=8.6 Hz). 13C NMR (75 MHz, CDCl3, ppm) =37.6, 54.7, 54.7, 56.2, 109.7, 116.2, 117.4, 125.1, 128.3, 154.9, 165.1, 167.3, 188.5. IR (neat, cm-1)=952, 1019, 1090, 1240, 1308, 1340, 1443, 1492, 1650, 1716, 1745, 2247, 2844, 2956. HRMS: calcd. for C13H11NO4Na [M+Na]=268.0578; found=268.0580.

(64) Compound 21

(65) Using the general procedure, compound 21 was prepared from 4,4,4-trifluoro-1-(furan-2-yl)butane-1,3-dione (45 L, 0.30 mmol), DIPEA (89 L, 0.51 mmol) and 8 (147 mg, 0.46 mmol) to obtain after flash chromatography (n-Hexane/EtOAc 8/2) as a yellow solid (40 mg, 99%). 1H NMR (300 MHz, CDCl3, ppm) =3.88 (2H, s), 6.57 (1H, dd, J=3.7, 1.7 Hz), 7.31 (1H, dd, J=3.7, 0.7 Hz), 7.59 (1H, dd, J=1.7, 0.7 Hz). 13C NMR (75 MHz, CDCl3, ppm) =29.8, 113.5, 119.4, 147.8, 147.9, 150.6, 175.8. IR (neat, cm-1)=881, 903, 941, 995, 1015, 1082, 1163, 1259, 1330, 1387, 1461, 1561, 1671, 1850, 2258, 2927, 2957, 3126, 3140. HRMS: calcd. for C7H5N1O2Na [M+Na]=158.0212; found=158.0212.

(66) Compound 22

(67) In a 2-necked round bottom flask, compound 8 (1.79 g, 5.59 mmol) was added to a solution of freshly distilled 1-cyclohexene-pyrrolidine (0.9 mL, 5.59 mmol) and DIPEA (1.0 mL, 5.59 mmol) in DCM (18 mL) at RT. After stirring 1 hour, the reaction was quenched with HCl (1N) and thoroughly extracted with Et2O. The organic layers were dried over Na2SO4, filtered and all the volatiles were removed under vacuum. The pure product was obtained by distillation (88 C., 0.1 mbar) as a colorless oil (379 mg, 55%). 1H NMR (ketone form) (300 MHz, CDCl3, ppm) =1.65-1.89 (3H, m), 1.96-2.15 (3H, m), 2.31-2.48 (2H, m), 3.50 (1H, dd, J=10.7, 5.4 Hz). 13C NMR (ketone) (75 MHz, CDCl3, ppm) =23.6, 26.7, 32.0, 40.6, 43.3, 116.5, 200.3. 1H NMR (enol form) (300 MHz, CDCl3, ppm) =1.90-1.95 (4H, m), 3.35-3.45 (4H, m). 13C NMR (enol) (75 MHz, CDCl3, ppm) =23.7, 25.8, 26.9, 32.2, 40.7, 43.4, 50.6, 116.7, 200.4. IR (neat, ketone/enol, cm-1)=949, 1036, 1073, 1127, 1160, 1205, 1300, 1352, 1379, 1425, 1450, 1666, 1690, 2202, 2250, 2869, 2945. HRMS: calcd. for C7H9NONa [M+Na]=146.0576; found=146.0576.

(68) Compound 23

(69) NaH (20 mg, 0.86 mmol) was added to a solution of 2-phenyl-1,1-diphenylsulfonethane4 (103 mg, 0.27 mmol) in dry THF (1.9 mL) at 0 C. After stirring for 5 minutes, 8 (131 mg, 0.41 mmol) was added and the reaction mixture warmed up to room temperature for 24 h. Then it was quenched with HCl (1N) and extracted with EtOAc. The organic layers were dried over anhydrous Na2SO4, filtered and the volatiles removed under vacuum. The crude oil thus obtained was purified by flash chromatography on silica gel (n-Hexane/EtOAc 8/2) affording 24 (90 mg, 82%). 1H NMR (300 MHz, CDCl3, ppm) =3.68 (2H, s), 7.03-7.23 (5H, m), 7.43-7.56 (4H, m), 7.61-7.71 (3H, m), 7.86-7.96 (3H, m). 13C NMR (75 MHz, CDCl3, ppm) =36.2, 84.4, 113.0, 128.5, 128.7, 129.3, 130.8, 131.5, 131.6, 135.8, 135.9. IR (neat, cm-1)=910, 999, 1024, 1076, 1170, 1314, 1354, 1448, 1497, 1582, 2256, 2924, 3065. HRMS: calcd. for C21H17NO4S2Na [M+Na]=434.0493; found=434.0491.

(70) General Procedure for Electrophilic Cyanation of Aromatic Substrates (Method B) A Young flask charged with the aromatic substrate (0.3-0.4 mmol), cyano source 9 (1.2 eq), BF3.Et2O (0.2 eq.) and dry DCE (0.10 M) was heated to 80 C. and stirred for the specified time. The reaction was quenched with NaHCO3 (sat.) and extracted with DCM. The combined organic layers were dried over anhydrous Na2SO4, filtered and all the volatiles removed in vacuum. The crude product was purified by flash chromatography on silica gel (n-Hexane/EtOAc).
Compound 24

(71) Using the general procedure, compound 24 was obtained as a colorless oil (51 mg, 87%) from 1-methylindole (48 L, 0.38 mmol), BF3.Et20 (9 L, 0.076 mmol) and 9 (216 mg, 0.45 mmol). Flash chromatography (n-Hexane/EtOAc 1/1). 1H NMR (400 MHz, CDCl3, ppm) =3.84 (3H, s), 7.27-7.35 (2H, m), 7.40 (1H, d, J=7.5 Hz), 7.43 (1H, s), 7.65 (1H, d, J=7.2 Hz). HRMS: calcd. for C10H8N2 [M]=156.0687; found=156.0689.

(72) Compound 25

(73) Using the general procedure, compound 25 was prepared from 1-methyl-2-phenylindole (62 mg, 0.30 mmol), BF3.Et2O (7 L, 0.060 mmol) and 9 (170 mg, 0.36 mmol), and purified by flash chromatography (n-Hexane/EtOAc 7/3) to obtain a white solid (64 mg, 92%). 1H NMR (400 MHz, CDCl3, ppm) =3.77 (3H, s), 7.33 (1H, ddd, J=7.4, 7.0, 1.3 Hz), 7.38 (1H, ddd, J=7.2, 6.9, 1.4 Hz), 7.43 (1H, brd, J=7.8 Hz), 7.50-7.62 (5H, m), 7.79 (1H, brd, J=7.6 Hz). 13C NMR (101 MHz, CDCl3, ppm) =31.7, 85.6, 110.4, 116.5, 119.6, 122.4, 123.8, 127.6, 128.7, 129.0, 129.8, 129.9, 136.8, 148.0. HRMS: calcd. for C16H12N2Na1 [M+Na]=255.0891; found=255.0892.

(74) Compound 26

(75) Using the general procedure, compound 26 was prepared from 1-phenylpyrrole (51 L, 0.35 mmol), BF3.Et20 (8 L, 0.070 mmol) and 9 (199 mg, 0.42 mmol). After flash chromatography (n-Hexane/EtOAc 7/3) a white solid was obtained (44 mg, 75%). 1H NMR (400 MHz, CDCl3, ppm) =6.36 (1H, dd, J=3.9, 2.8 Hz), 7.00 (1H, dd, J=4.0, 1.5 Hz), 7.09 (1H, dd, J=2.8, 1.6 Hz), 7.41-7.52 (5H, m). HRMS: calcd. for C11H8N2 [M]=168.0687; found=168.0689.

(76) Compound 27

(77) Using the general procedure, compound 27 was prepared from 1,2,5-trimethylpyrrole (54 L, 0.40 mmol), BF3.Et2O (10 L, 0.080 mmol) and compound 9 (227 mg, 0.48 mmol). After flash chromatography (n-Hexane/EtOAc 8/2) a pale yellow solid was obtained (45 mg, 83%). 1H NMR (400 MHz, CDCl3, ppm) =2.19 (3H, s), 2.33 (3H, s), 3.40 (3H, s), 6.02 (1H, q, J=1.0 Hz). 13C NMR (101 MHz, CDCl3, ppm) =10.1, 10.2, 20.8, 94.6, 110.7, 117.3, 128.0, 136.6. IR (neat, cm-1)=1239, 1342, 1369, 1416, 1437, 1535, 1702, 1737, 2148, 2207, 2850, 2919, 2961. HRMS: calcd. for C8H10N2 [M]=134.0844; found=134.0845.

(78) Compound 28

(79) Using the general procedure, compound 28 was prepared from 1,3-dimethoxybenzene (47 L, 0.36 mmol), BF3.Et2O (9 L, 0.072 mmol) and 9 (204 mg, 0.43 mmol). After flash chromatography (n-Hexane/EtOAc 8/2) a white solid was obtained (50 mg, 86%). 1H NMR (400 MHz, CDCl3, ppm) =3.84 (3H, s), 3.88 (3H, s), 6.45 (1H, d, J=2.0 Hz), 6.51 (1H, dd, J=8.4, 2.2 Hz), 7.47 (1H, d, J=8.7 Hz). HRMS: calcd. for C9H9NO2 [M]=163.0633; found=163.0634.

(80) Compound 29

(81) Using the general procedure, compound 29 was prepared from 1,3,5-trimethoxybenzene (59 mg, 0.35 mmol), BF3.Et2O (9 L, 0.072 mmol) and 9 (200 mg, 0.42 mmol). After flash chromatography (n-Hexane/EtOAc 8/2) a white solid was obtained (63 mg, 94%). 1H NMR (400 MHz, CDCl3, ppm) =3.85 (3H, s), 3.88 (6H, s), 6.06 (2H, s). 13C NMR (101 MHz, CDCl3, ppm) =54.9, 55.3, 83.2, 89.5, 113.9, 163.0, 164.5. IR (neat, cm-1)=917, 951, 1022, 1051, 1157, 1211, 1227, 1347, 1413, 1467, 1496, 1579, 1603, 1940, 2211, 2848, 2946, 2979. HRMS: calcd. for C10H11N1O3Na1 [M+Na]=216.0629; found=216.0631.

(82) Compound 30

(83) Using the general procedure, compound 30 was prepared from 1,3-dimethoxyphenanthrene5 (71 mg, 0.30 mmol), BF3.Et2O (7 L, 0.060 mmol) and 9 (170 mg, 0.36 mmol). After flash chromatography (n-Hexane/EtOAc 8/2) a yellow solid was obtained (73 mg, 93%). 1H NMR (600 MHz, CDCl3, ppm) =4.04 (3H, s), 4.07 (3H, s), 6.62 (1H, s), 7.61-7.71 (3H, m), 7.86-7.90 (1H, m), 8.06 (1H, d, J=9.0 Hz), 9.79-9.83 (1H, m). 13C NMR (151 MHz, CDCl3, ppm) =56.1, 56.6, 86.7, 91.9, 118.5, 119.5, 119.8, 125.5, 125.8, 126.5, 128.1, 128.3, 128.8, 131.8, 134.0, 160.8, 165.1. IR (neat, cm-1)=1122, 1244, 1279, 1309, 1346, 1384, 1416, 1427, 1459, 1506, 1526, 1568, 1591, 1620, 2206, 2940. HRMS: calcd. for C17H13N1O2Na1 [M+Na]=286.0837; found=286.0838.

(84) Compound 31

(85) Using the general procedure, compound 31 was prepared from 3,3,5,5-tetramethoxy-1,1-biphenyl6 (82 mg, 0.30 mmol), BF3.Et2O (7 L, 0.060 mmol) and 9 (170 mg, 0.36 mmol). After flash chromatography (n-Hexane/EtOAc 8/2) a pale yellow solid (62 mg, 70%) was obtained. 1H NMR (400 MHz, CDCl3, ppm) =3.83 (6H, s), 3.88 (3H, s), 3.94 (3H, s), 6.46 (1H, d, J=2.2 Hz), 6.52 (1H, t, J=2.3 Hz), 6.56 (1H, d, J=2.2 Hz.) 6.67 (1H, d, J=2.3 Hz). HRMS: calcd. for C17H17N1O4Na1 [M+Na]=322.1046; found=322.1049.

(86) Compound 32

(87) Using the general procedure, compound 32 was prepared from anthracene (55 mg, 0.31 mmol), BF3.Et2O (7 L, 0.062 mmol) and 9 (175 mg, 0.37 mmol). After flash chromatography (n-Hexane/EtOAc 7/3) a yellow solid (29 mg, 46%) was obtained. 1H NMR (400 MHz, CDCl3, ppm) =7.60 (2H, ddd, J=8.6, 6.6, 1.1 Hz), 7.73 (2H, ddd, J=8.7, 6.6, 1.2 Hz), 8.09 (2H, d, J=8.5 Hz), 8.42 (2H, brdd, J=8.6, 1.0 Hz), 8.70 (1H, s). HRMS: calcd. for C15H9N1 [M]=203.0736; found=203.0734.

(88) Compound 33

(89) Using the general procedure, compound 33 was prepared from tetracene (75 mg, 0.33 mmol), BF3.Et2O (8 L, 0.066 mmol) and 9 (188 mg, 0.39 mmol). After flash chromatography (n-Hexane/EtOAc from 9:1 to 7:3) a red solid was obtained (70 mg, 84%). 1H NMR (400 MHz, CDCl3, ppm) =7.47-7.55 (3H, m), 7.68 (1H, ddd, J=8.9, 6.6, 1.2 Hz), 7.97-8.18 (3H, m), 8.39 (1H, dd, J=8.8, 1.0 Hz), 8.76 (1H, s), 8.92 (1H, s), 9.06 (1H, s). HRMS: calcd. for C19H11N1Na1 [M+Na]=276.0784; found=276.0783.

(90) Compound 35

(91) Silver ethyl propiolate (1.41 g, 6.87 mmol) was added to a solution of compound 5 (2.56 g, 6.87 mmol) in dry DCM (20 mL) at RT (note: the reaction is slightly exothermic and may cause DCM to boil). After 5 min AgSbF6 (2.32 g, 6.75 mmol) was added and the reaction mixture stirred at RT for 45 min. Silver salts were then filtered off and the solvent removed under vacuum. The remaining solid was washed twice with diethyl ether to afford compound 36 as a pale yellow solid (3.48 g, 93%). 1H NMR (400 MHz, CD3CN, ppm) =1.24 (3H, t, J=7.1 Hz), 1.62 (12H, d, J=7.0 Hz), 2.38 (6H, s), 4.21 (2H, q, J=7.1 Hz), 5.17 (2H, hept, J=7.0 Hz). 13C NMR (101 MHz, CD3CN, ppm) =10.6, 14.1, 21.0, 54.8, 63.7, 73.4, 87.8, 128.6, 132.6, 152.5. 19F NMR (282 MHz, CD3CN) =124.00 (sext, JF-121Sb=1931 Hz). IR (neat, cm-1)=1026, 1115, 1140, 1219, 1261, 1380, 1397, 1460, 1615, 1707, 2178, 2989. HRMS: calcd. for C16H25N2O2S1 [M-SbF6]=309.1629; found=309.1631.

(92) General Procedure for Alkynylation Reaction

(93) Reagent 35 (1.2 eq) was added to a solution of initial substrate (0.30 mmol) and DIPEA (1.0 eq) in dry DCM (0.15 M) and the reaction was stirred at room temperature for the specified time (see Chart 2). The reaction was quenched with NH4Cl (1.0 M) and extracted with DCM. The organic layers were dried over anhydrous Na2SO4, filtered and all the volatiles removed under vacuum. The crude was purified by flash chromatography on silica gel (n-Hexane/EtOAc) affording the desired products.

(94) Compound 36

(95) Using the general procedure, compound 36 was prepared from 4-(trifluoromethyl) benzenethiol (50 L, 0.36 mmol), DIPEA (63 L, 0.36 mmol) and 35 (235 mg, 0.43 mmol), obtaining after flash chromatography (n-Hexane/EtOAc 8/2) a yellow oil (97 mg, 98%). 1H NMR (400 MHz, CD2Cl2, ppm) =1.32 (3H, t, J=7.1 Hz), 4.26 (2H, q, J=7.2 Hz), 7.61 (2H, d, J=8.4 Hz), 7.67 (2H, d, J=8.4 Hz). 13C NMR (101 MHz, CD2012, ppm) =14.2, 62.6, 77.2, 93.2, 125.6 (q, JC-F=272.0 Hz) 126.8 (q, JC-F=3.7 Hz) 127.3, 130.0 (q, JC-F=32.7 Hz), 152.8, 163.2; IR (neat, cm-1)=1013, 1032, 1085, 1165, 1367, 1403, 1466, 1541, 1606, 1703, 2153, 2984. HRMS calcd. for C12H10O2SF3 [M+H]=275.0346; found=275.0348.

(96) Compound 37

(97) Using the general procedure, compound 37 was prepared from methyl thioglycolate (34 L, 0.38 mmol), DIPEA (66 L, 0.38 mmol) and compound 35 (248 mg, 0.45 mmol) obtaining after flash chromatography (n-Hexane/EtOAc 8/2) an orange oil (72 mg, 94%). 1H NMR (400 MHz, CDCl3, ppm) =1.30 (3H, t, J=7.2 Hz), 3.66 (2H, s), 3.81 (3H, s), 4.23 (2H, q, J=7.2 Hz). 13C NMR (101 MHz, CDCl3, ppm) =13.9, 36.7, 52.9, 61.7, 80.9, 88.4, 152.5, 167.5. IR (neat, cm-1)=1030, 1163, 1296, 1366, 1391, 1436, 1698, 1738, 2149, 2955, 2983. HRMS calcd. for C8H10O4S1Na1 [M+Na]=225.0191; found=225.0192.

(98) Compound 38

(99) Using the general procedure, compound 38 was prepared from 4-methoxybenzenethiol (39 L, 0.32 mmol), DIPEA (56 L, 0.32 mmol) and compound 36 (209 mg, 0.38 mmol) obtaining after flash chromatography (n-Hexane/EtOAc 8/2) a yellow oil (74 mg, 98%). 1H NMR (400 MHz, CDCl3, ppm) =1.31 (3H, t, J=7.1 Hz), 3.81 (3H, s), 4.24 (2H, q, J=7.1 Hz), 6.88-6.97 (2H, m), 7.35-7.46 (2H, m). 13C NMR (101 MHz, CDCl3, ppm) =13.0, 54.4, 60.8, 80.6, 88.8, 114.3, 118.1, 129.4, 151.9, 158.9. IR (neat, cm-1): 914, 1023, 1054, 1091, 1120, 1239, 1378, 1411, 1426, 1551, 1624, 1719, 2158, 2975. HRMS calcd. for C12H12O3S1Na1 [M+Na]=259.0397; found=259.0399.

(100) Compound 39

(101) NaH (21 mg, 0.76 mmol) was added to a solution of 1,3-dimethylindolin-2-one (111 mg, 0.69 mmol) in dry THF (4.6 mL) at 0 C. After stirring for 30 minutes, 35 (569 mg, 1.04 mmol) was added and the reaction mixture was left to warm up to room temperature for 3 h. Then it was quenched with HCl (1N) and extracted with EtOAc. The organic layers were dried over anhydrous Na2SO4, filtered and the volatiles were removed in vacuum. The crude was purified by flash chromatography on silica gel (n-Hexane/EtOAc 8/2) affording 40 (140 mg, 79%). 1H NMR (400 MHz, CDCl3, ppm) =1.24 (3H, t, J=7.1 Hz), 1.69 (3H, s), 3.20 (3H, s), 4.16 (2H, q, J=7.1 Hz), 6.84 (1H, d, J=7.7 Hz), 7.09 (1H, dt, J=7.4, 0.9 Hz), 7.26-7.38 (2H, m). 13C NMR (101 MHz, CDCl3, ppm) =14.0, 24.7, 26.9, 42.7, 62.2, 74.1, 85.2, 108.8, 123.5, 123.6, 129.4, 130.1, 142.4, 153.3, 174.0. IR (neat, cm-1)=729, 791, 909, 1030, 1093, 1223, 1256, 1278, 1345, 1367, 1470, 1491, 1610, 1709, 2234, 2964.

(102) Compound 40

(103) DIPEA (61 L, 0.35 mmol) was added to a solution of methyl 1-oxo-2,3-dihydro-1H-indene-2-carboxylate (66 mg, 0.35 mmol) in dry DCM (0.15 M). After stirring for 15 min, compound 35 (229 mg, 0.42 mmol) was added and the reaction was allowed to stir for 30 min. The reaction was then quenched with NH4Cl and extracted with DCM. The organic layers were dried over anhydrous Na2SO4, filtered and the volatiles were removed in vacuum. The crude was purified by flash chromatography on silica gel (n-Hexane/EtOAc from 9/1 to 7/3) affording 40 as an orange oil (89 mg, 89%). 1H NMR (400 MHz, CDCl3, ppm) =1.29 (3H, t, J=7.1 Hz), 3.58 (1H, d, =17.2 Hz), 3.83 (3H, s), 3.97 (1H, d, J=17.2 Hz), 4.22 (2H, q, J=7.2 Hz), 7.45 (1H, ddd, J=7.9, 7.1, 0.9 Hz), 7.50 (1H, dt, J=7.9, 0.9 Hz), 7.69 (1H, td, J=7.5, 1.2 Hz), 7.82 (1H, dt, J=7.5, 1.2 Hz). 13C NMR (101 MHz, CDCl3, ppm) =14.1, 40.0, 54.3, 62.4, 75.6, 82.8, 126.2, 126.6, 128.4, 128.7, 132.9, 136.5, 152.1, 153.2, 167.2, 194.2. IR (neat, cm-1)=956, 1021, 1103, 1211, 1235, 1291, 1342, 1368, 1418, 1435, 1463, 1604, 1740, 2973. HRMS: calcd. for C16H14O5Na [M+Na]=309.0734; found=309.0733.

(104) As shown above, the present invention provides imidazolium sulfuranes to become reference platforms for the development of new reagents able to promote the reverse reaction of synthetically useful organic groups. The studies of the inventors have shown the generality of the concept and the substrate scope and synthetic utility of these new reagents in the presence of metal-based catalysts.