Diaza-benzofluoranthrene compounds

Abstract

Disclosed are a series of diaza-benzofluoranthrene compounds. The present invention particularly relates to a compound represented by formula (I), pharmaceutically acceptable salts or tautomers thereof.

Claims

1. A compound of formula (I), or a pharmaceutically acceptable salt or a tautomer thereof, ##STR00246## wherein: R.sub.1 and R.sub.3 are separately and independently selected from H; or R.sub.1 and R.sub.3 are separately and independently selected from the group, optionally substituted by R.sub.01, consisting of S(O).sub.2NH.sub.2 or C.sub.1-4 alkyl; R.sub.2 is selected from ##STR00247## wherein: from zero to two of T.sub.21-23 is N, and the rest is C(R.sub.t); D.sub.21 is selected fromC(R.sub.d1)(R.sub.d2), C(O)N(R.sub.d3), N(R.sub.d4), C(NR.sub.d5), S(O).sub.2N(R.sub.d6), S(O)N(R.sub.d7), O, S, C(O)O,C(O)-,C(S)-, S(O), S(O).sub.2 or N(R.sub.d8)C(O)N(R.sub.d9); T.sub.24 is selected from N or C(R.sub.t); D.sub.22-24 are separately and independently selected from C(R.sub.d1)(R.sub.d2), C(O)N(R.sub.d3), N(R.sub.d4), C(NR.sub.d5), S(O).sub.2N(R.sub.d6), S(O)N(R.sub.d7), O, S, C(O)O, C(O), C(S), S(O), S(O).sub.2 or N(R.sub.d8)C(O)N(R.sub.d9); from zero to two of T.sub.25-29 is N, and the rest is C(R.sub.t); optionally, any two of R.sub.t and R.sub.d1-d9 are bonded to a common atom or group together to form one or two 3- to 8-membered rings; R.sub.t, R.sub.d1 and R.sub.d2 are separately and independently selected from H, F, Cl, Br, I, CN, OH, SH, NH.sub.2, CHO, COOH, C(O)NH.sub.2, S(O)NH.sub.2, or S(O).sub.2NH.sub.2; or R.sub.t, R.sub.d1 and R.sub.d2 are separately and independently selected from the group, optionally substituted by R.sub.01, consisting of C.sub.1-10 alkyl, C.sub.1-10 alkyl heteroalkyl, C.sub.3-10 cyclic hydrocarbyl, or C.sub.3-10 heterocyclic hydrocarbyl, C.sub.1-10 alkyl substituted by C.sub.3-10 cyclohydrocarbyl or C.sub.3-10 heterocyclohydrocarbyl, C.sub.1-10 heteroalkyl substituted by C.sub.3-10 cyclohydrocarbyl or C.sub.3-10 heterocyclohydrocarbyl, C.sub.1-10 alkenyl, and C.sub.1-10 heteroalkenyl; R.sub.01 is selected from F, Cl, Br, I, CN, OH, SH, NH.sub.2, CHO, COOH, C(O)NH.sub.2, S(O)NH.sub.2, S(O).sub.2NH.sub.2 or R.sub.02; R.sub.02 is selected from C.sub.1-10 alkyl, C.sub.1-10 heteroalkyl, C.sub.3-10 cycloalkyl, C.sub.3-10 heterocyclic alkyl, aminoacyl, or a 5- to 12-membered unsaturated heterocyclic group; hetero- represents a hetero atom or a hetero atom-containing group, which is selected from the group consisting of C(O)N(R.sub.d3), N(R.sub.d4), C(NR.sub.d5), S(O).sub.2N(R.sub.d6).sup., S(O)N(R.sub.d7), O, S, O, S, C(O)O, C(O), C(S), S(O), S(O).sub.2 and N(R.sub.d8)C(O)N(R.sub.d9); R.sub.d3-d9 are separately and independently selected from H, NH.sub.2, or R.sub.02; R.sub.02 is optionally substituted by R.sub.001; R.sub.001 is selected from F, Cl, Br, I, CN, OH, N(CH.sub.3).sub.2, NH(CH.sub.3), NH.sub.2, CHO, COOH, C(O)NH.sub.2, S(O)NH.sub.2, S(O).sub.2NH.sub.2, trifluoromethyl, aminomethyl, hydroxymethyl, methyl, methoxy, formyl, methoxycarbonyl, methanesulfonyl, or methylsulfinyl; the number of R.sub.01, R.sub.001, the hetero atom or the hetero atom-containing group are separately and independently selected from 0, 1, 2, 3, or 4.

2. The compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 1, wherein: R.sub.1 and R.sub.3 are separately and independently selected from the group consisting of H, ##STR00248##

3. The compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 1, wherein R.sub.2 is separately and independently selected from ##STR00249## wherein A represents 6-membered saturated or unsaturated carbocycle or heterocycle, each optionally substituted by 0, 1, 2 or 3 R.sub.t.

4. The compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 3, wherein R.sub.2 is separately and independently selected from ##STR00250##

5. The compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 1, wherein R.sub.t and R.sub.d1-d9 are separately and independently selected from H, NH.sub.2, or CN; or C.sub.1-6 alkyl, C.sub.1-6 heteroalkyl, C.sub.3-6 cycloalkyl, C.sub.3-6 heterocyclic alkyl, a 5- or 6-membered unsaturated heterocyclic group, or aminoacyl, each optionally substituted by R.sub.001; R.sub.t and R.sub.d1-d2 are separately and independently selected from F, Cl, Br, or I; R.sub.t and R.sub.d1-d9 are preferably separately and independently selected from C.sub.1-6 alkylamino, N,N-di(C.sub.1-3 alkyl) amino, C.sub.1-6 alkoxy, C.sub.1-6 alkanoyl, C.sub.1-6 alkoxycarbonyl, C.sub.1-6 alkylsulfonyl, C.sub.1-6 alkylsulfinyl, C.sub.3-6 cycloalkyl, C.sub.3-6 cycloalkylamino, C.sub.3-6 heterocyclic alkylamino, C.sub.3-6 cycloalkoxy, C.sub.3-6 cycloalkyl acyl, C.sub.3-6 cyclic alkoxycarbonyl, C.sub.3-6 cycloalkylsulfonyl, C.sub.3-6 cycloalkylsulfinyl, aminoacyl, or 5- to 6-membered unsaturated heterocyclyl, each optionally substituted by R.sub.001; R.sub.t and R.sub.d1-d9 are more preferably separately and independently selected from 5- to 6-membered aryl or 5- to 6-membered heteroaryl, each optionally substituted by R.sub.001; R.sub.t and R.sub.d1-d9 are more preferably separately and independently selected from phenyl, pyridyl or thienyl, each optionally substituted by R.sub.001.

6. The compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 5, wherein the hetero atom or the hetero atom-containing group is selected from O, N, S, C(O)O, or ##STR00251##

7. The compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 6, wherein R.sub.t and R.sub.d1-d9 are separately and independently selected from H, F, Cl, Br, I, NH.sub.2, CH.sub.3, CN, ##STR00252##

8. The compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 7, wherein R.sub.1-3 are separately and independently selected from: ##STR00253## ##STR00254## ##STR00255##

9. The compound, or the pharmaceutically acceptable salt or the tautomers thereof according to claim 1 selected from: ##STR00256## ##STR00257## ##STR00258## ##STR00259## ##STR00260## ##STR00261## ##STR00262## ##STR00263## ##STR00264## ##STR00265## ##STR00266## ##STR00267## ##STR00268## ##STR00269##

10. A method of treating cerebral apoplexy or epilepsy in a subject, comprising administering to the subject a therapeutically effective amount of the compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 1.

11. A method of treating cerebral apoplexy or epilepsy in a subject, comprising administering to the subject a therapeutically effective amount of the compound, or the pharmaceutically acceptable salt or tautomer thereof according to claim 2.

12. A method of treating cerebral apoplexy or epilepsy in a subject, comprising administering to the subject a therapeutically effective amount of the compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 3.

13. A method of treating cerebral apoplexy or epilepsy in a subject, comprising administering to the subject a therapeutically effective amount of the compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 4.

14. A method of treating cerebral apoplexy or epilepsy in a subject, comprising administering to the subject a therapeutically effective amount of the compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 5.

15. A method of treating cerebral apoplexy or epilepsy in a subject, comprising administering to the subject a therapeutically effective amount of the compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 6.

16. A method of treating cerebral apoplexy or epilepsy in a subject, comprising administering to the subject a therapeutically effective amount of the compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 7.

17. A method of treating cerebral apoplexy or epilepsy in a subject, comprising administering to the subject a therapeutically effective amount of the compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 8.

18. A method of treating cerebral apoplexy or epilepsy in a subject, comprising administering to the subject a therapeutically effective amount of the compound, or the pharmaceutically acceptable salt or the tautomer thereof according to claim 9.

Description

DETAILED DESCRIPTION OF ILLUSTRATED EMBODIMENTS

(1) The present invention will be described in detail in combination with the following preferred embodiments, and it will be appreciated that such embodiments are merely exemplary, the invention is not to be limited to the disclosed embodiments.

(2) ##STR00068##

Example 1

1-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolyl[3,2,1-de]pyridyl[3,2,1-ij][1,5]naphthyridine-12-yl)-2,2,2-trifluoroethanol

(3) ##STR00069##

Example 1A

((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolyl[3,2,1-de]pyridyl[3,2,1-ij][1,5]naphthyridine-12-yl) methanol

(4) ##STR00070##

(5) Lithium aluminum hydride (3.2 g, 85.7 mmol) was added in batches to the tetrahydrofuran solution (400 ml) of vinpocetine (10 g, 28.6 gmmol) under 0-5 C., the reaction mixture was stirred for 30 minutes under room temperature and nitrogen atmosphere. After completion, the reaction was quenched with 5 ml water, and 4 ml 2M sodium hydroxide solution and 4 ml water was added to the reaction mixture. The precipitated product was filtered out, water and ethyl acetate was added to extract the concentrated filtrate. The extract was dried and concentrated to obtain the target compound.

(6) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 0.98 (t, J=7.53 Hz, 3H), 1.08-1.17 (m, 1H), 1.38-1.48 (m, 2H), 1.65-1.82 (m, 2H), 1.86-1.96 (m, 1H), 2.51 (ddd, J=16.00, 4.96, 1.88 Hz, 1H), 2.62-2.76 (m, 2H), 2.98-3.09 (m, 1H), 3.20-3.29 (m, 1H), 3.32-3.39 (m, 1H), 4.16 (br. s., 1H), 4.61 (d, J=13.30 Hz, 1H), 4.83 (d, J=13.30 Hz, 1H), 5.11 (s, 1H), 7.10-7.15 (m, 1H), 7.20 (td, J=7.72, 1.38 Hz, 1H), 7.47 (d, J=7.78 Hz, 1H), 7.67 (d, J=8.53 Hz, 1H).

Example 1B

((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolyl[3,2,1-de]pyridyl[3,2,1-ij][1,5]naphthyridine-12-methanal

(7) ##STR00071##

(8) Active manganese dioxide (5.07 g, 58.4 mmol) was added to the dichloromethane solution (20 ml) of ((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolyl[3,2,1-de]pyridyl[3,2,1-ij][1,5]naphthyridine-12-yl) methanol (1.8 g, 5.84 mmol), the reaction mixture was heated and stirred overnight, then filtered, and the filtrate was concentrated. The residue was subjected to column chromatography, eluting with a mixed solution of petroleum ether/ethyl acetate (10/1 by volume) to obtain the target compound (colorless oil, 1.2 g, yield 67.1%).

Example 1C

1-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolyl[3,2,1-de]pyridyl[3,2,1-ij][1,5]naphthyridine-12-yl-2,2,2,-trifluoroethanol

(9) ##STR00072##

(10) Cesium fluoride (148.73 mg, 0.979 mmol) and (trifluoromethyl) trimethylsilane (139.2 mg, 0.979 mmol) was added to the anhydrous tetrahydrofuran solution (5 ml) of ((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolyl[3,2,1-de]pyridyl[3,2,1-ij][1,5]naphthyridine-12) methanal (200 mg, 0.652 mmol) at 0 C., the reaction mixture was stirred for 1 h at 0 C., then tetrabutylammonium fluoride was added, the mixture was stirred for 1 h under room temperature and then concentrated. The residue was subjected to Preparative High Performance Liquid Chromatography to obtain the target compound (100m g, yield 40.8%).

(11) .sup.1H NMR (CD.sub.3OD, 400 MHz) 7.59 (d, J=8.0 Hz, 1H), 7.43 (d, J=8.0 Hz, 1H), 7.137.17 (m, 1H), 7.057.09 (m, 1H), 5.545.61 (m, 2H), 4.18 (s, 1H), 3.243.28 (m, 2H), 2.962.98 (m, 1H), 2.532.67 (m, 3H), 1.751.98 (m, 1H), 1.701.74 (m, 2H), 1.441.51 (m, 2H), 0.991.08 (m, 4H).

(12) LCMS (ESI) m/z: 377 (M+1)

(13) ##STR00073##

Example 2

(41S,13aS,Z)-13a-ethyl-N-methoxyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carbimidoyl cyanide

(14) ##STR00074##

Example 2A

(15) ##STR00075##

(16) To a solution of ((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl) methyl methanesulfonate (3.8 g, 12.3 mmol) in tetrahydrofuran (80 mL) was added triethylamine (1.9 g, 18.5 mmol) and methanesulfonyl chloride (1.1 mL, 14.8 mmol) at 0-5 C. under an atmosphere of nitrogen, the reaction mixture was heated to room temperature and stirred for 1 hour. After completion, the ammonium chloride solution was added to the reaction mixture. The mixture was extracted with ethyl acetate, the extracts were dried and concentrated to obtain the target compound (yellow solid, 5 g, crude product, for the next step).

Example 2B

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl) acetonitrile

(17) ##STR00076##

(18) The crude product (5 g, 12.9 mmol) obtained from the previous step was dissolved in dimethylsulfoxide (40 ml), then sodium cyanide (3.2 g, 64.8 mmol) was added and the reaction mixture was stirred overnight at room temperature. After completion, the mixture was poured into 150 ml water, and the precipitated solid was filtered out and dried to obtain the target compound (yellow solid, 3.6 g, yield: 88%).

(19) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 0.94-1.02 (m, 4H), 1.38-1.50 (m, 2H), 1.69-1.80 (m, 2H), 2.03 (dq, J=14.62, 7.51 Hz, 1H), 2.37-2.45 (m, 1H), 2.48-2.62 (m, 3H), 2.88-2.98 (m, 1H), 3.11 (d, J=15.06 Hz, 1H), 3.20-3.36 (m, 2H), 3.98 (s, 1H), 5.62 (d, J=1.76 Hz, 1H), 7.25-7.33 (m, 2H), 7.47-7.52 (m, 1H), 7.65 (d, J=7.53 Hz, 1H).

Example 2C

(41S,13aS,Z)-13a-ethyl-N-methoxyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carbimidoyl cyanide

(20) ##STR00077##

(21) To a solution of 2-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl) acetonitrile (300 mg, 0.95 mmol) in tetrahydrofuran (20 mL) was successively added isoamyl nitrite (332 mg, 0.95 mmol) and potassium tert-butoxide (424 mg, 3.8 mmol), and the reaction mixture was stirred at room temperature under an atmosphere of nitrogen for 1 hour. Potassium iodide (538 mg, 3.8 mmol) was added to the reaction mixture, and the mixture was stirred for another 3 hours. After completion, water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extracts were dried and concentrated. The residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (100 mg, yield: 29%).

(22) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 1.07-1.30 (m, 4H), 1.62-1.73 (m, 2H), 2.17-2.35 (m, 3H), 2.90-3.20 (m, 3H), 3.31 (br. s., 1H), 3.58-3.84 (m, 2H), 4.22 (s, 3H), 4.72 (br. s., 1H), 5.75 (s, 1H), 7.20-7.26 (m, 2H), 7.28-7.33 (m, 1H), 7.47-7.56 (m, 1H).

(23) ##STR00078##

Example 3

(41S,13aS)-13a-ethyl-12-(1H-imidazol-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(24) ##STR00079##

(25) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carbaldehyde (300 mg, 0.97 mmol) in anhydrous ethanol (5 mL) was added glyoxal (568 mg, 0.97 mmol) and aqueous ammonia (343 mg, 9.79 mmol), respectively, and the reaction mixture was heated under reflux for 3 days. The reaction mixture was concentrated and the residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (50 mg, yield: 14.8%)

(26) .sup.1H NMR (CD3OD, 400 MHz) ppm 7.75 (s, 2H), 7.64 (d, J=8.0 Hz, 1H), 7.14-7.24 (m, 2H), 6.11 (d, J=8.0 Hz, 1H), 5.98 (s, 1H), 5.16 (s, 1H), 3.86-3.96 (m, 2H), 3.35-3.38 (m, 2H), 3.16-3.27 (m, 2H), 1.96-2.04 (m, 3H), 1.79-1.87 (m, 2H), 1.38 (m, 1H), 1.12 (t, J=9.8 Hz, 3H).

(27) LCMS (ESI) m/z: 345 (M+1)

(28) ##STR00080##

Example 4

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)oxazole

(29) ##STR00081##

(30) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carbaldehyde (500 mg, 1.63 mmol) in methanol (6 mL) was successively added sodium methoxide (450 mg, 8.15 mmol) and (p-tolylsulfonyl)methyl isocyanide (390 mg, 2 mmol) at room temperature, and the reaction mixture was refluxed overnight. After cooling, the mixture was concentrated, and the residue was treated with sodium bicarbonate solution, and then was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated and the crude product was purified by silica gel chromatography to obtain the target compound (200 mg, yield: 35.6%).

(31) .sup.1H NMR (400 MHz, DMSO) ppm 8.58 (s, 1H), 7.59-7.35 (m, 2H), 7.09-6.85 (m, 2H), 6.12 (d, J=8.1 Hz, 1H), 5.52 (s, 1H), 4.10 (q, J=5.1 Hz, 1H), 3.20-3.09 (m, 3H), 2.94 (br. s., 1H), 1.94-1.73 (m, 2H), 1.59 (br. s., 1H), 1.50 (d, J=13.0 Hz, 1H), 1.38 (br. s., 1H), 0.97-0.85 (m, 3H).

(32) LCMS (ESI) m/z: 346 (M+1)

(33) ##STR00082##

Example 5

(E)-3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)acrylic acid

(34) ##STR00083##

(35) A solution of triethyl phosphonoacetate (293 mg, 1.3 mmol) in 2 mL tetrahydrofuran was cooled to 0 C. with an ice-water bath, then sodium hydride (60%, 80 mg, 2 mmol) was added thereto, then a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carbaldehyde (200 mg, 0.65 mmol) in 2 mL tetrahydrofuran was added thereto after about half an hour, and the reaction mixture was slowly heated to room temperature and stirred overnight. After completion (monitored by TLC), the solvent was distilled off, and the residue was dissolved in 2 mL dimethylsulfoxide. The target compound (17 mg, yield: 7.56%) was separated by Preparative High Performance Liquid Chromatography.

(36) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.71-7.60 (m, 1H), 7.52 (t, J=7.9 Hz, 2H), 7.28-7.13 (m, 2H), 6.38 (d, J=15.6 Hz, 1H), 5.51 (s, 1H), 3.73 (d, J=7.0 Hz, 3H), 3.09 (br. s., 6H), 2.17-1.89 (m, 3H), 1.69 (d, J=12.3 Hz, 2H), 1.31-1.16 (m, 2H), 1.10 (t, J=7.3 Hz, 3H).

(37) LCMS (ESI) m/z: 349 (M+1)

Example 6

(E)-ethyl-3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)acrylate

(38) ##STR00084##

(39) To a solution of (E)-3-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)acrylic acid (200 mg, 0.573 mmol) in 5 mL tetrahydrofuran was added potassium carbonate (158 mg, 1.14 mmol) and iodoethane (88 mg, 0.57 mmol), respectively, and the reaction mixture was stirred at room temperature overnight. After completion (monitored by TLC), the solvent was distilled off, and the residue was dissolved in 2 mL dimethylsulfoxide. The target compound was separated by Preparative High Performance Liquid Chromatography.

(40) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.67 (d, J=15.6 Hz, 1H), 7.44-7.24 (m, 2H), 7.15-6.96 (m, 2H), 6.28 (d, J=15.8 Hz, 1H), 5.52 (s, 1H), 4.27 (d, J=7.0 Hz, 2H), 3.85 (br. s., 1H), 3.24-3.11 (m, 1H), 3.08-2.79 (m, 2H), 2.55-2.32 (m, 3H), 1.90-1.67 (m, 2H), 1.67-1.51 (m, 1H), 1.46-1.22 (m, 5H), 0.98 (t, J=7.4 Hz, 3H), 0.90-0.77 (m, 1H).

(41) LCMS (ESI) m/z: 377 (M+1)

(42) ##STR00085##

Example 7

(E)-3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)acrylamide

(43) ##STR00086##

(44) To a mixture of (E)-3-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)acrylic acid (200 mg, 0.57 mmol), ammonium chloride (36 mg, 0.688 mmol) and 5 mL tetrahydrofuran was added triethylamine (69 mg, 0.68 mmol) and 2-(7-azobenzotriazole)-N,N,N,N-tetramethyluronium hexafluophosphate (217 mg, 0.57 mmol), respectively, the reaction mixture was stirred at room temperature for 1 hour, and then the mixture was heated to 60 C. and stirred overnight. After completion (monitored by TLC), the solvent was distilled off, and the residue was dissolved in 2 mL dimethylsulfoxide. The target compound was separated by Preparative High Performance Liquid Chromatography.

(45) .sup.1H NMR (400 MHz, MeOD) ppm 7.66 (d, J=15.3 Hz, 1H), 7.43 (dd, J=7.9, 12.7 Hz, 2H), 7.25-6.99 (m, 2H), 6.49 (d, J=15.6 Hz, 1H), 5.53 (s, 1H), 4.17 (br. s., 1H), 3.27-3.16 (m, 1H), 3.03 (br. s., 1H), 2.72-2.49 (m, 3H), 2.04-1.64 (m, 3H), 1.57-1.36 (m, 2H), 1.04 (t, J=7.3 Hz, 4H).

(46) LCMS (ESI) m/z: 348 (M+1)

(47) ##STR00087##

Example 8

(41S,13aS)-13a-ethyl-12-(4-methylpyrimidin-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(48) ##STR00088##

Example 8A

(41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylic acid

(49) ##STR00089##

(50) To a mixture of sodium hydroxide (137 mg, 3.43 mmol) and anhydrous dioxane (14 mL) was added vinpocetine (1 g, 2.86 mmol) at 80 C., and the mixture was reacted at such temperature for 2 hours. After vinpocetine was consumed (monitored by TLC), the mixture was concentrated to dry, water was added to dissolve the residue, the pH of the solution obtained was adjusted to 3 with 2M hydrochloric acid. The mixture was extracted with a mixed solution of dichloromethane/isopropanol (10/1 by volume), the extract was dried and concentrated to obtain the target compound (for the next step, 900 mg, yield: 98%).

(51) LCMS (ESI) m/z: 323 (M+1)

Example 8B

(41S,13aS)-13a-ethyl-12-(4-methylpyrimidin-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(52) ##STR00090##

(53) To a microwave tube was added (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylic acid (300 mg, 0.93 mmol), 2-chloro-4-methylpyrimidine (180 mg, 1.396 mmol), cesium carbonate (363 mg, 1.117 mmol) and 1,10-phenanthroline (8.4 mg, 0.047 mmol), the mixture was uniformly mixed with N-methylpyrrolidone (3 mL) and then purged three times with nitrogen. Copper(I) iodide (8.9 mg, 0.047 mmol) and palladium (II) acetylacetonate (14 mg, 0.047 mmol) were added, then the tube was sealed. The reaction mixture was heated to 170 C. with microwave and reacted for 30 minutes. The reaction mixture was poured into 20 mL water and filtered, and the filter cake was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (100 mg, yield: 29%).

(54) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 8.77 (d, J=5.3 Hz, 1H), 7.60 (d, J=7.8 Hz, 1H), 7.53 (d, J=5.3 Hz, 1H), 7.15 (t, J=7.5 Hz, 1H), 7.07-7.01 (m, 1H), 6.21 (d, J=8.3 Hz, 1H), 5.90 (s, 1H), 5.15 (s, 1H), 3.99-3.90 (m, 1H), 3.90-3.83 (m, 1H), 3.36 (d, J=3.5 Hz, 1H), 3.31-3.26 (m, 1H), 3.23-3.15 (m, 1H), 2.61 (s, 3H), 2.09-1.91 (m, 3H), 1.90-1.77 (m, 2H), 1.36 (dt, J=3.1, 13.7 Hz, 1H), 1.13 (t, J=7.3 Hz, 3H).

(55) LCMS (ESI) m/z: 371 (M+1)

Example 9

(41S,13aS)-13a-ethyl-12-(6-methylpyridazin-3-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(56) ##STR00091##

(57) The preparation method of the example was the same as that of Example 8B.

(58) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 8.57-8.51 (m, 1H), 8.50-8.45 (m, 1H), 7.63 (d, J=7.5 Hz, 1H), 7.21-7.15 (m, 1H), 7.13-7.08 (m, 1H), 6.50 (d, J=8.3 Hz, 1H), 6.02 (s, 1H), 5.19 (s, 1H), 3.97-3.82 (m, 2H), 3.38-3.33 (m, 1H), 3.28-3.14 (m, 2H), 3.01 (s, 3H), 2.13-1.95 (m, 3H), 1.91-1.77 (m, 2H), 1.36 (dt, J=3.3, 13.8 Hz, 1H), 1.13 (t, J=7.3 Hz, 3H).

(59) LCMS (ESI) m/z: 371 (M+1)

Example 10

(41S,13aS)-13a-ethyl-12-(6-methylpyrazin-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(60) ##STR00092##

(61) The preparation method of the example was the same as that of Example 8B.

(62) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 8.67 (d, J=11.8 Hz, 2H), 7.61 (d, J=7.8 Hz, 1H), 7.15 (t, J=7.5 Hz, 1H), 7.06-6.97 (m, 1H), 6.13 (d, J=8.3 Hz, 1H), 5.67 (s, 1H), 5.18 (s, 1H), 4.00-3.91 (m, 1H), 3.90-3.84 (m, 1H), 3.38-3.34 (m, 1H), 3.31-3.27 (m, 1H), 3.24-3.16 (m, 1H), 2.60 (s, 3H), 2.08-1.91 (m, 3H), 1.90-1.78 (m, 2H), 1.46-1.36 (m, 1H), 1.14 (t, J=7.4 Hz, 3H).

(63) LCMS (ESI) m/z: 371 (M+1)

Example 11

(41S,13aS)-13a-ethyl-12-(pyridin-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrid o[3,2,1-ij][1,5]naphthyridine

(64) ##STR00093##

(65) The preparation method of the example was the same as that of Example 8B.

(66) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 8.99 (d, J=5.3 Hz, 1H), 8.79 (t, J=7.7 Hz, 1H), 8.31-8.23 (m, 2H), 7.68 (d, J=7.8 Hz, 1H), 7.23 (t, J=7.5 Hz, 1H), 7.12 (t, J=7.5 Hz, 1H), 6.22 (d, J=8.3 Hz, 1H), 6.07 (s, 1H), 5.23 (br. s., 1H), 4.02-3.93 (m, 1H), 3.92-3.86 (m, 1H), 3.42-3.34 (m, 2H), 3.30-3.19 (m, 2H), 2.14-1.99 (m, 3H), 1.92 (d, J=14.3 Hz, 1H), 1.84 (d, J=14.3 Hz, 1H), 1.40 (dt, J=3.4, 13.9 Hz, 1H), 1.17 (t, J=7.4 Hz, 3H).

(67) LCMS (ESI) m/z: 356 (M+1)

Example 12

(41S,13aS)-13a-ethyl-12-(6-methylpyridin-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(68) ##STR00094##

(69) The preparation method of the example was the same as that of Example 8B.

(70) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 8.57 (t, J=8.0 Hz, 1H), 8.10-7.95 (m, 2H), 7.65 (d, J=7.8 Hz, 1H), 7.20 (t, J=7.3 Hz, 1H), 7.13-7.06 (m, 1H), 6.21 (d, J=8.3 Hz, 1H), 6.00 (s, 1H), 5.21 (s, 1H), 4.00-3.91 (m, 1H), 3.90-3.82 (m, 1H), 3.41-3.32 (m, 2H), 3.30-3.24 (m, 1H), 3.24-3.17 (m, 1H), 2.86 (s, 3H), 2.16-1.95 (m, 3H), 1.94-1.77 (m, 2H), 1.40 (dt, J=3.3, 13.9 Hz, 1H), 1.15 (t, J=7.4 Hz, 3H).

(71) LCMS (ESI) m/z: 370 (M+1)

Example 13

(41S,13aS)-13a-ethyl-12-(3-methylpyridin-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(72) ##STR00095##

(73) The preparation method of the example was the same as that of Example 8B.

(74) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 8.95 (d, J=5.5 Hz, 1H), 8.62 (d, J=8.0 Hz, 1H), 8.27-8.18 (m, 1H), 7.64 (d, J=7.8 Hz, 1H), 7.22-7.14 (m, 1H), 7.08-6.99 (m, 1H), 6.00 (d, J=8.5 Hz, 0.67H), 5.90-5.82 (m, 1H), 5.73 (d, J=8.3 Hz, 0.33H), 5.38-5.24 (m, 1H), 4.02-3.84 (m, 2H), 3.43-3.32 (m, 2H), 3.30-3.26 (m, 1H), 3.24-3.16 (m, 1H), 2.69 (s, 1H), 2.21 (s, 2H), 2.17-2.08 (m, 1H), 2.07-1.81 (m, 4H), 1.60-1.45 (m, 1H), 1.14 (t, J=7.4 Hz, 3H).

(75) LCMS (ESI) m/z: 370 (M+1)

Example 14

(41S,13aS)-12-(5,6-dimethylpyrazin-2-yl)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(76) ##STR00096##

(77) The preparation method of the example was the same as that of Example 8B.

(78) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 8.69 (s, 1H), 7.61 (d, J=7.8 Hz, 1H), 7.19-7.12 (m, 1H), 7.04 (t, J=7.8 Hz, 1H), 6.30 (d, J=8.3 Hz, 1H), 5.75 (s, 1H), 5.17 (br. s., 1H), 3.99-3.83 (m, 2H), 3.40-3.16 (m, 4H), 2.78 (s, 3H), 2.67 (s, 3H), 2.12-1.95 (m, 3H), 1.90-1.79 (m, 2H), 1.39 (t, J=12.5 Hz, 1H), 1.14 (t, J=7.3 Hz, 3H).

(79) LCMS (ESI) m/z: 385 (M+1)

(80) ##STR00097##

Example 15

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,3,4-oxadiazole

(81) ##STR00098##

Example 15A

(41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-hydrazide

(82) ##STR00099##

(83) Thionyl chloride (20 mL) was added dropwise to a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylic acid (1.8 g, 5.58 mmol) and DMF (1 mL) in chloroform (15 mL) at 0 C., then the reaction mixture was heated under reflux and maintained for 3 hours. After cooling to room temperature, the reaction mixture was poured into 25% hydrazine hydrate (1.4 g, 27.9 mmol) and stirred for another 2 hours. The mixture was diluted with water and extracted with dichloromethane. The extract was dried over anhydrous sodium sulfate and concentrated to obtain the target compound (yellow solid, 1.7 g, yield: 89%).

Example 15B

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,3,4-oxadiazole

(84) ##STR00100##

(85) A mixture of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-hydrazide (400 mg, 1.2 mmol) and trimethyl orthoformate (5 mL) was heated to 160 C. with microwave and reacted for half an hour. The reaction mixture was concentrated to dry, and the crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (50 mg, yield: 12%).

(86) .sup.1H NMR (400 MHz, CDCl.sub.3) ppm 1.02 (t, J=7.28 Hz, 3H), 1.17 (td, J=13.55, 3.51 Hz, 1H), 1.26 (s, 1H), 1.45 (d, J=13.05 Hz, 1H), 1.60 (d, J=14.05 Hz, 1H), 1.69-1.79 (m, 1H), 1.90-2.01 (m, 2H), 2.54 (d, J=16.31, 3.26 Hz, 1H), 2.63-2.69 (m, 2H), 2.99-3.11 (m, 1H), 3.26-3.41 (m, 2H), 4.25 (s, 1H), 5.99 (s, 1H), 6.52 (d, J=8.53 Hz, 1H), 7.03-7.15 (m, 2H), 7.49 (d, J=7.53 Hz, 1H), 8.57 (s, 1H).

(87) LCMS (ESI) m/z: 346 (M+1)

Example 16

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,3,4-oxadiazol-2(3H)-one

(88) ##STR00101##

(89) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-hydrazide (170 mg, 0.5 mmol) in dioxane (7 ml) was added carbonyl diimidazole (98 mg, 0.6 mmol), and the mixture was heated under reflux for 45 minutes. After the reaction mixture was concentrated, the residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (42 mg, yield: 23%).

(90) .sup.1H NMR (400 MHz, CDCl.sub.3) ppm 0.90 (t, J=7.21 Hz, 3H), 1.40 (d, J=13.69 Hz, 1H), 1.50 (d, J=13.69 Hz, 1H), 1.77-1.96 (m, 4H), 2.11 (s, 1H), 2.56 (t, J=11.00 Hz, 1H), 2.68 (s, 1H), 2.76 (d, J=10.27 Hz, 1H), 3.23 (d, J=6.36 Hz, 2H), 4.37 (br. s., 1H), 5.23 (s, 1H), 5.81 (s, 1H), 7.13 (d, J=3.67 Hz, 1H), 7.17-7.22 (m, 1H), 7.31-7.36 (m, 1H).

(91) LCMS (ESI) m/z: 362 (M+1)

Example 17

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-methyl-1,3,4-oxadiazole

(92) ##STR00102##

(93) To a 50 mL round bottom flask was added (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-hydrazide (500 mg, 1.5 mmol), triethyl orthoacetate (487 mg, 3 mmol) and acetic acid (5 mL), and the reaction mixture was refluxed for 30 min. After completion (monitored by LC-MS), the solvent was distilled off, and the residue was dissolved in 2 mL dimethylsulfoxide. The target compound (200 mg, yield: 31.1%) was separated by Preparative High Performance Liquid Chromatography.

(94) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 1.12 (t, J=7.28 Hz, 3H), 1.24-1.37 (m, 1H), 1.70-1.85 (m, 2H), 1.89-2.12 (m, 3H), 2.56-2.74 (m, 5H), 3.08-3.29 (m, 3H), 3.84 (d, J=5.27 Hz, 2H), 5.14 (br. s., 1H), 6.08 (s, 1H), 6.78 (d, J=8.78 Hz, 1H), 7.1-7.28 (m, 2H), 7.55-7.68 (in, 1H).

(95) LCMS (ESI) m/z: 363 (M+1)

(96) ##STR00103## ##STR00104##

Example 18

3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazol-5 (4H)-one

(97) ##STR00105##

Example 18A

(41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxamide

(98) ##STR00106##

(99) Thionyl chloride (5 mL) was added dropwise to a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylic acid (4 g, 12.4 mmol) and DMF (0.1 mL) in chloroform (40 mL), then the reaction mixture was heated under reflux and maintained for 3 hours. After cooling to room temperature, the reaction mixture was poured into 25% ammonium hydroxide (40 mL) and stirred for 2 hours. The mixture was diluted with water and extracted with dichloromethane. The extract was dried over anhydrous sodium sulfate and concentrated to obtain the target compound (yellow solid, 3.8 g, yield: 95%).

(100) .sup.1H NMR (400 MHz, CDCl.sub.3) ppm 7.44 (d, J=6.8 Hz, 1H), 7.36 (d, J=8.0 Hz, 1H), 7.09-7.15 (m, 2H), 5.91-6.10 (m, 2H), 5.84 (s, 1H), 4.14 (s, 1H), 3.32-3.41 (m, 1H), 3.19-3.31 (m, 1H), 2.89-3.09 (m, 1H), 2.58-2.68 (m, 2H), 2.44-2.55 (m, 1H), 1.84-1.96 (m, 3H), 1.65-1.77 (m, 1H), 1.47-1.50 (m, 1H), 1.39-1.42 (m, 1H), 1.01 (t, J=8.0 Hz, 3H).

(101) LCMS (ESI) m/z: 322 (M+1)

Example 18B

(41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carbonitrile

(102) ##STR00107##

(103) Phosphorus oxychloride was added dropwise to a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxamide (3.8 g, 11.8 mmol) in chloroform (50 mL) at 0 C., and the mixture was heated under reflux for 4 hours. After cooling to room temperature, the mixture was poured into ice water, and the pH of the mixture was adjusted to neutral with 40% sodium hydroxide solution. The organic layer was separated, and the remaining aqueous layer was extracted with dichloromethane. The combined organic layers were washed with sodium bicarbonate solution, dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was recrystallized with a mixed solution of isopropanol/water (1/1 by volume) to obtain the target compound (yellow solid, 2.0 g, yield: 56%).

(104) .sup.1H NMR (400 MHz, CDCl.sub.3) ppm 7.94 (d, J=8.0 Hz, 1H), 7.40 (d, J=8.0 Hz, 1H), 7.17-7.21 (m, 1H), 7.10-7.13 (m, 1H), 5.86 (s, 1H), 4.16 (s, 1H), 3.27-3.32 (m, 1H), 3.14-3.23 (m, 1H), 2.91-2.98 (m, 1H), 2.61 (d, J=4.0 Hz, 2H), 2.42-2.47 (m, 1H), 1.87-1.99 (m, 1H), 1.70-1.81 (m, 2H), 1.39-1.48 (m, 2H), 1.01-1.09 (m, 1H), 0.95 (t, J=8.0 Hz, 3H).

(105) LCMS (ESI) m/z: 304 (M+1)

Example 18C

(41S,13aS,Z)-13a-ethyl-N-hydroxyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxamidine

(106) ##STR00108##

(107) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carbonitrile (300 mg, 1 mmol) in methanol (8 mL) was added hydroxylamine hydrochloride (350 mg, 5 mmol) and diisopropylethylamine (323 mg, 2.5 mmol), respectively, the reaction mixture was stirred at room temperature for 2 hours, then hydroxylamine hydrochloride (175 mg, 2.5 mmol) was added, and the reaction mixture was stirred for another 5 hours. Hydroxylamine hydrochloride (175 mg, 2.5 mmol) was added and the reaction mixture was stirred at room temperature for 17 hours. After completion, a small amount of water was added to the mixture, then the mixture was filtered. The solid obtained was washed with ethyl acetate and then dissolved in methanol. The solvent was distilled off to obtain the pure target compound (white solid, 300 mg, yield: 89%).

(108) .sup.1H NMR (400 MHz, MeOD) ppm 1.10 (t, J=7.39 Hz, 3H), 1.21-1.33 (m, 2H), 1.34-1.39 (m, 1H), 1.73 (d, J=11.69 Hz, 3H), 1.85-1.92 (m, 2H), 1.98 (dt, J=14.55, 7.28 Hz, 2H), 3.06-3.13 (m, 1H), 3.21-3.26 (m, 2H), 3.34 (s, 1H), 3.79-3.85 (m, 2H), 5.03 (br. s., 1H), 5.49 (s, 1H), 7.13-7.19 (m, 1H), 7.22 (t, J=7.28 Hz, 1H), 7.38 (d, J=8.38 Hz, 1H), 7.54 (d, J=7.72 Hz, 1H).

Example 18D

3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazol-5 (4H)-one

(109) ##STR00109##

(110) To a solution of (4.sup.1S,13aS, Z)-13a-ethyl-N-hydroxyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxamidine (200 mg, 0.6 mmol) in dioxane (10 mL) was added carbonyl diimidazole (482 mg, 3.0 mmol), and the reaction mixture was heated under reflux for 45 minutes. After the solvent was distilled off, the residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (127 mg, yield: 58%).

(111) .sup.1H NMR (400 MHz, CDCl3) ppm 1.00 (s, 3H), 1.26 (d, J=13.55 Hz, 1H), 1.72 (d, J=15.06 Hz, 2H), 1.92 (s, 4H), 3.06 (s, 3H), 3.26 (s, 1H), 3.47 (s, 1H), 3.60 (s, 1H), 4.86 (s, 1H), 5.85 (s, 1H), 7.08 (d, J=7.53 Hz, 1H), 7.16-7.25 (m, 2H), 7.40-7.55 (m, 1H).

(112) LCMS (ESI) m/z: 362 (M+1)

Example 19

3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-thiadiazol-5(4H)-one

(113) ##STR00110##

(114) A solution of (4.sup.1S,13aS, Z)-13a-ethyl-N-hydroxyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxamidine (200 mg, 0.6 mmol) and thiocarbonyldiimidazole in tetrahydrofuran (15 mL) was heated to 60 C. and stirred for 1.5 hours. The reaction mixture was concentrated, and the residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (69 mg, yield: 31%).

(115) .sup.1H NMR (400 MHz, CDCl.sub.3) ppm 1.02 (br. s., 3H), 1.14-1.31 (m, 2H), 1.58 (d, J=14.11 Hz, 1H), 1.72 (d, J=13.45 Hz, 1H), 2.03 (br. s., 1H), 2.90 (d, J=11.03 Hz, 2H), 3.14 (br. s., 2H), 3.47 (d, J=2.43 Hz, 1H), 3.56 (br. s., 1H), 4.85 (br. s., 1H), 5.77 (br. s., 1H), 6.81 (br. s., 1H), 7.15 (br. s., 2H), 7.41 (br. s., 1H).

(116) LCMS (ESI) m/z: 378 (M+1)

Example 20

3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-methyl-1,2,4-oxadiazole

(117) ##STR00111##

(118) To a 50 mL round bottom flask were added (4.sup.1S,13aS, Z)-13a-ethyl-N-hydroxyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxamidine (150 mg, 0.45 mmol), acetic anhydride (136.6 mg, 0.134 mmol) and acetic acid (10 mL), respectively, and the reaction mixture was stirred at 110 C. for 1 hour. After the reaction mixture was concentrated, the residue was dissolved in 1 mL N,N-dimethylformamide. The target compound was obtained by Preparative High Performance Liquid Chromatography (17 mg, yield: 10.7%).

(119) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.61-7.55 (m, 1H), 7.20-7.10 (m, 2H), 6.87-6.78 (m, 1H), 5.95 (s, 1H), 5.14 (s, 1H), 3.94-3.76 (m, 2H), 3.29-3.23 (m, 2H), 3.19-3.11 (m, 1H), 2.71 (s, 3H), 2.06-1.99 (m, 1H), 1.99-1.91 (m, 2H), 1.83-1.74 (m, 2H), 1.37-1.29 (m, 2H), 1.11 (t, J=7.4 Hz, 3H).

(120) LCMS (ESI) m/z: 361 (M+1)

Example 21

3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-trifluoromethyl-1,2,4-oxadiazole

(121) ##STR00112##

(122) To a solution of (4.sup.1S,13aS, Z)-13a-ethyl-N-hydroxyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxamidine (700 mg, 2.083 mmol) in tetrahydrofuran (20 mL) was added pyridine (822.92 mg, 10.417 mmol) and trifluoroacetic anhydride (2177.08 mg, 10.417 mmol), and the reaction mixture was stirred at 10 C. for 3 hours. After completion, the solvent was removed under reduced pressure, water was added to the residue, then the mixture obtained was extracted with ethyl acetate. After the extract was concentrated, the crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (400 mg, yield: 46.4%).

(123) .sup.1H NMR (400 MHz, Methanol-d4) ppm 7.63-7.59 (m, 1H), 7.21-7.19 (m, 2H), 7.01-6.99 (m, 1H), 6.20 (s, 1H), 5.10 (s, 1H), 3.84-3.82 (m, 2H), 3.32-3.16 (m, 4H), 2.08-2.00 (m, 3H), 1.98-1.79 (m, 2H), 1.30-1.15 (m, 1H), 1.13-1.11 (m, 3H).

(124) LCMS (ESI) m/z: 415 (M+1)

Example 22

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-3-trifluoromethyl-1,2,4-oxadiazole

(125) ##STR00113##

(126) To a solution of 3-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-trifluoromethyl-1,2,4-oxadiazole (300 mg, 0.725 mmol) in N,N-dimethylformamide was added hydroxylamine hydrochloride (150 mg, 2.174 mmol) and potassium tert-butoxide (243.93 mg, 2.174 mmol), respectively, and the reaction mixture was stirred at 40 C. for 5 hours. The reaction mixture was filtered, and potassium tert-butoxide (150.62 mg, 1.342 mmol) was added to the filtrate. The mixture obtained was heated to 100 C. and stirred for 1 hour. After cooling to room temperature, the mixture was diluted with water and extracted three times with ethyl acetate. The combined extracts were washed with brine and concentrated. The residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (30 mg, yield: 10%).

(127) .sup.1H NMR (400 MHz, Methanol-d4) ppm 7.65-7.63 (m, 1H), 7.27-7.21 (m, 2H), 6.92-6.90 (m, 1H), 6.51 (s, 1H), 5.16 (s, 1H), 3.94-3.85 (m, 2H), 3.33-3.16 (m, 4H), 2.12-2.03 (m, 3H), 1.99-1.84 (m, 2H), 1.33-1.17 (m, 1H), 1.15-1.14 (m, 3H).

(128) LCMS (ESI) m/z: 415 (M+1)

(129) ##STR00114##

Example 23

3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-(tetrahydro-2H-pyran-4-yl)-1,2,4-oxadiazole

(130) ##STR00115##

(131) A mixture of diisopropylethylamine (288 mg, 2.23 mmol), tetrahydropyran-4-carboxylic acid (116 mg, 0.89 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (340 mg, 1.78 mmol), 1-hydroxybenzotriazole (120 mg, 0.89 mmol) and N,N-dimethylformamide (4 mL) was stirred at 15 C. for 1 hour, then (4.sup.1S,13aS, Z)-13a-ethyl-N-hydroxyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxamidine (250 mg, 0.74 mmol) was added, and the mixture was stirred for another 16 hours. The reaction mixture was extracted with a mixture of dichloromethane/methanol (10/1 by volume), and the extracts were concentrated. The residue was purified by Preparative Thin Layer Chromatography (a mixture of dichloromethane/methanol (10/1 by volume) as a developing solvent) to obtain the intermediate amide (white solid, 205 mg, yield: 62%).

(132) The intermediate amide (205 mg, 0.45 mmol) was dissolved in toluene (15 mL), then potassium tert-butoxide (167 mg, 1.49 mmol) was added. The mixture was heated under reflux and stirred overnight. After cooling to 15 C., the mixture was concentrated. The residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (70 mg, yield: 36%).

(133) .sup.1H NMR (CDCl.sub.3, 400 MHz) ppm 12.00 (br. s., 1H), 7.66-8.09 (m, 2H), 7.49 (d, J=7.0 Hz, 1H), 7.17 (q, J=6.9 Hz, 2H), 6.78 (d, J=7.8 Hz, 1H), 5.85-5.98 (m, 1H), 4.95 (br. s., 1H), 4.06 (d, J=11.7 Hz, 2H), 3.74-3.87 (m, 2H), 3.58 (t, J=11.3 Hz, 2H), 3.45 (d, J=11.3 Hz, 1H), 3.26-3.36 (m, 1H), 3.01-3.22 (m, 3H), 1.94-2.15 (m, 7H), 1.63-1.81 (m, 2H), 1.25-1.39 (m, 1H), 1.04 (t, J=7.2 Hz, 3H).

(134) LCMS (ESI) m/z: 431 (M+1)

Example 24

3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-(pyridin-4-yl)-1,2,4-oxadiazole

(135) ##STR00116##

(136) The preparation method of the example was the same as that of Example 23.

(137) .sup.1H NMR (CDCl.sub.3, 400 MHz) ppm 11.54 (br. s., 1H), 9.00 (d, J=5.1 Hz, 2H), 8.35 (d, J=5.5 Hz, 2H), 7.43-7.57 (m, 1H), 7.13-7.18 (m, 2H), 6.83 (d, J=8.2 Hz, 1H), 6.04 (s, 1H), 4.99 (br. s., 1H), 3.71-3.89 (m, 2H), 3.46 (d, J=11.0 Hz, 1H), 3.03-3.21 (m, 3H), 1.90-2.13 (m, 3H), 1.64-1.81 (m, 2H), 1.27-1.40 (m, 1H), 1.02 (t, J=7.0 Hz, 3H).

(138) LCMS (ESI) m/z: 424 (M+1)

Example 25

2-(3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazol-5-yl)propan-2-ol

(139) ##STR00117##

(140) The preparation method of the example was the same as that of Example 23.

(141) .sup.1H NMR (MeOD, 400 MHz) ppm 7.46 (d, J=8.0 Hz, 1H), 6.97-7.15 (m, 2H), 6.65 (d, J=8.5 Hz, 1H), 5.87 (s, 1H), 4.33 (br. s., 1H), 3.03-3.15 (m, 1H), 2.53-2.77 (m, 3H), 1.87-2.05 (m, 2H), 1.69-1.83 (m, 7H), 1.49-1.66 (m, 2H), 1.10-1.20 (m, 2H), 1.05 (t, J=7.5 Hz, 3H).

(142) LCMS (ESI) m/z: 405 (M+1)

Example 26

Tert-butyl-4-(3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazol-5-yl)piperidine-1-carboxylate

(143) ##STR00118##

(144) The preparation method of the example was the same as that of Example 23.

(145) .sup.1H NMR (MeOD, 400 MHz) ppm 7.46 (d, J=7.5 Hz, 1H), 6.95-7.13 (m, 2H), 6.64 (d, J=8.0 Hz, 1H), 5.85 (s, 1H), 4.32 (br. s., 1H), 4.07-4.14 (m, 2H), 3.35-3.45 (m, 2H), 3.07 (d, J=7.0 Hz, 3H), 2.57-2.75 (m, 3H), 2.15 (d, J=14.1 Hz, 2H), 1.72-2.01 (m, 5H), 1.63 (d, J=13.6 Hz, 1H), 1.01-1.19 (m, 4H).

(146) LCMS (ESI) m/z: 530 (M+1)

Example 27

3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-(4-fluorophenyl)-1,2,4-oxadiazole

(147) ##STR00119##

(148) The preparation method of the example was the same as that of Example 23.

(149) .sup.1H NMR (MeOD, 400 MHz) ppm 8.24 (dd, J=5.3, 8.8 Hz, 2H), 7.28-7.50 (m, 3H), 6.93-7.11 (m, 2H), 6.76 (d, J=8.2 Hz, 1H), 5.94 (s, 1H), 4.40 (br. s., 1H), 3.39 (d, J=5.5 Hz, 2H), 3.04-3.14 (m, 1H), 2.61-2.79 (m, 3H), 1.89-2.01 (m, 2H), 1.77 (d, J=12.9 Hz, 1H), 1.65 (d, J=13.7 Hz, 1H), 1.51 (d, J=13.3 Hz, 1H), 1.16 (d, J=3.1 Hz, 1H), 1.04 (t, J=7.4 Hz, 3H).

(150) LCMS (ESI) m/z: 441 (M+1)

Example 28

3-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-(thiophen-2-yl)-1,2,4-oxadiazole

(151) ##STR00120##

(152) The preparation method of the example was the same as that of Example 23.

(153) .sup.1H NMR (MeOD, 400 MHz,) ppm 8.06 (d, J=3.5 Hz, 1H), 7.94 (d, J=5.0 Hz, 1H), 7.47 (d, J=7.5 Hz, 1H), 7.33 (t, J=4.3 Hz, 1H), 6.98-7.11 (m, 2H), 6.80 (d, J=8.0 Hz, 1H), 5.95 (s, 1H), 4.34 (br. s., 1H), 3.03-3.18 (m, 1H), 2.56-2.77 (m, 3H), 1.87-2.08 (m, 2H), 1.78 (d, J=14.1 Hz, 1H), 1.65 (d, J=14.1 Hz, 1H), 1.50 (d, J=13.6 Hz, 1H), 1.11-1.21 (m, 1H), 1.06 (t, J=7.3 Hz, 3H).

(154) LCMS (ESI) m/z: 429 (M+1)

(155) ##STR00121##

Example 29

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-3-methyl-1,2,4-oxadiazole

(156) ##STR00122##

(157) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylic acid (14 g, 43.4 mmol), 1-hydroxybenzotriazole (300 mg, 2.17 mmol) and triethylamine (31 mL, 217 mmol) in N,N-dimethylformamide (200 mL) was added O-(benzotriazol-1-yl)-N,N,N,N-tetramethyluronium tetrafluoroborate (14.6 g, 45.6 mmol) and N-hydroxyacetamidine hydrochloride (5.28 g, 47.8 mmol), respectively, and the reaction mixture was stirred at room temperature overnight. Brine was added to the reaction mixture, then the mixture obtained was filtered, and the filtrate was diluted with water and extracted with dichloromethane. The extract was dried over anhydrous sodium sulfate, and the low boiling components were distilled off. The remaining crude product in N,N-dimethylformamide was directly heated to 160 C. with microwaves and reacted for 50 min. The crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (4.0 g, yield: 25%).

(158) .sup.1H NMR (CDCl.sub.3, 400 MHz) ppm 7.46 (d, J=6.8 Hz, 1H), 7.13-7.06 (m, 2H), 6.73 (d, J=8.0 Hz, 1H), 6.08 (s, 1H), 4.23 (s, 1H), 3.38-3.34 (m, 2H), 3.29-3.28 (m, 2H), 2.65-2.63 (m, 2H), 2.55-2.51 (m, 1H), 2.51 (s, 3H), 1.97-1.92 (m, 2H), 1.59-1.55 (m, 2H), 1.45-1.41 (m, 1H), 1.11-1.10 (m, 1H), 1.00 (t, J=7.2 Hz, 3H).

(159) LCMS (ESI) m/z: 361 (M+1)

Example 30

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-3-phenyl-1,2,4-oxadiazole

(160) ##STR00123##

(161) The preparation method of the example was the same as that of Example 29.

(162) .sup.1H NMR (CDCl.sub.3, 400 MHz) ppm 8.19-8.13 (m, 2H), 7.55-7.47 (m, 4H), 7.17-7.04 (m, 2H), 6.88 (d, J=7.94 Hz, 1H), 6.19 (s, 1H), 4.26 (br. s., 1H), 3.43-3.25 (m, 2H), 3.13-3.00 (m, 1H), 2.71-2.60 (m, 2H), 2.55 (dd, J=16.21, 2.98 Hz, 1H), 2.06-1.87 (m, 3H), 1.85-1.68 (m, 1H), 1.62 (d, J=13.45 Hz, 1H), 1.52-1.38 (m, 1H), 1.17 (td, J=13.67, 3.53 Hz, 1H), 1.04 (t, J=7.50 Hz, 3H).

(163) LCMS (ESI) m/z: 423 (M+1)

Example 31

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-3-(pyridin-4-yl)-1,2,4-oxadiazole

(164) ##STR00124##

(165) The preparation method of the example was the same as that of Example 29.

(166) .sup.1H NMR (400 MHz, CDCl.sub.3) ppm 8.83 (d, J=4.02 Hz, 2H), 8.02 (d, J=6.02 Hz, 2H), 7.54 (d, J=7.53 Hz, 1H), 7.16-7.24 (m, 1H), 6.87 (d, J=7.53 Hz, 1H), 6.26 (s, 1H), 5.30 (s, 1H), 4.69 (br. s., 1H), 3.62 (br. s., 1H), 3.22-3.06 (m, 2H), 2.89 (d, J=11.04 Hz, 2H), 2.03 (td, J=14.68, 6.78 Hz, 2H), 1.75 (d, J=14.05 Hz, 1H), 1.62 (d, J=13.55 Hz, 1H), 1.23-1.32 (m, 2H), 1.09 (t, J=7.28 Hz, 3H).

(167) LCMS (ESI) m/z: 424 (M+1)

Example 32

5-((4S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-3-(4-fluorophenyl)-1,2,4-oxadiazole

(168) ##STR00125##

(169) The preparation method of the example was the same as that of Example 29.

(170) .sup.1H NMR (400 MHz, CDCl.sub.3) ppm 8.16 (d, J=8.71, 5.40 Hz, 2H), 7.50 (d, J=7.50 Hz, 1H), 7.15-7.23 (m, 2H), 7.07-7.15 (m, 2H), 6.87 (d, J=7.94 Hz, 1H), 6.19 (s, 1H), 4.26 (br. s., 1H), 3.36-3.43 (m, 1H), 3.26-3.35 (m, 1H), 3.00-3.12 (m, 1H), 2.67 (d, J=6.39 Hz, 2H), 2.52-2.59 (m, 1H), 1.91-2.03 (m, 2H), 1.71-1.81 (m, 1H), 1.62 (d, J=13.67 Hz, 2H), 1.46 (d, J=13.23 Hz, 1H), 1.10-1.26 (m, 2H), 1.04 (t, J=7.39 Hz, 3H).

(171) LCMS (ESI) m/z: 440 (M+1)

Example 33

3-ethyl-5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazole

(172) ##STR00126##

(173) The preparation method of the example was the same as that of Example 29.

(174) .sup.1H NMR (400 MHz, Methanol-d4) ppm 7.61-7.59 (d, J=8.0 Hz, 1H), 7.23-7.16 (m, 2H), 6.75-6.73 (d, J=8.0 Hz, 1H), 6.22 (s, 1H), 5.05 (s, 1H), 3.80 (m, 2H), 3.30-3.13 (m, 4H), 2.89-2.85 (m, 2H), 2.09-1.98 (m, 3H), 1.77 (m, 2H), 1.41-1.37 (m, 1H), 1.36-1.25 (m, 1H), 1.14-1.10 (m, 3H).

Example 34

5-((4S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-3-isopropyl-1,2,4-oxadiazole

(175) ##STR00127##

(176) The preparation method of the example was the same as that of Example 29.

(177) .sup.1H NMR (400 MHz, Methanol-d4) ppm 7.63-7.61 (d, J=8.0 Hz, 1H), 7.24-7.17 (m, 2H), 6.74-6.72 (d, J=8.0 Hz, 1H), 6.24 (s, 1H), 5.14 (s, 1H), 3.93-3.85 (m, 2H), 3.32-3.20 (m, 5H), 2.07-1.99 (m, 3H), 1.83-1.79 (m, 2H), 1.43-1.40 (m, 6H), 1.32-1.30 (m, 1H), 1.16-1.12 (m, 3H).

Example 35

3-Cyclopropyl-5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrid o[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazole

(178) ##STR00128##

(179) The preparation method of the example was the same as that of Example 29.

(180) .sup.1H NMR (400 MHz, MeOD-d.sub.4) ppm 7.61 (d, J=6.5 Hz, 1H), 7.26-7.16 (m, 2H), 6.77-6.65 (m, 1H), 6.21 (s, 1H), 5.12 (br. s., 1H), 3.85 (d, J=5.0 Hz, 2H), 3.29-3.12 (m, 3H), 2.30-2.21 (m, 1H), 2.12-1.94 (m, 3H), 1.86-1.73 (m, 2H), 1.58-0.78 (m, 9H).

(181) LCMS (ESI) m/z: 387 (M+1)

(182) ##STR00129##

Example 36

3-Difluoromethyl-5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazole

(183) ##STR00130##

Example 36A

2,2-Diethoxy-N-hydroxyacetamidine

(184) ##STR00131##

(185) A mixture of hydroxylamine hydrochloride (2.674 g, 38.76 mmol) and sodium methoxide (2.093 g, 38.76 mmol) in methanol (20 mL) was stirred at 0 C. for half an hour, then heated to 25 C. and stirred for half an hour. Diethoxyacetonitrile (1 g, 7.752 mmol) was added, then the mixture was heated to 40 C. and stirred overnight. After the solvent was removed under reduced pressure, the residue was diluted with water and extracted with ethyl acetate (320 mL). The extracts were combined, washed with brine, dried over anhydrous sodium sulfate and concentrated to obtain the crude product of the target compound (colorless oil, 900 mg, yield: 71.6%).

Example 36B

(41S,13aS)-N-(2,2-diethoxy-1-(hydroxyimino)ethyl)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide

(186) ##STR00132##

(187) To a solution of 2,2-diethoxy-N-hydroxyacetamidine (600 mg, 3.529 mmol) in tetrahydrofuran (20 mL) was added (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-acyl chloride (1 g, 2.941 mmol, prepared by the method of Example 21A, and the excess thionyl chloride was distilled off). After completion, the low boiling-point component was distilled off obtain the crude product of the target compound (yellow solid, 1.6 g, yield: about 100%).

(188) LCMS(ESI) m/z: 467 (M+1)

Example 36C

3-diethoxymethyl-5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazole

(189) ##STR00133##

(190) A mixture of (4S,13aS)-N-(2,2-diethoxy-1-(hydroxyimino)ethyl)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide (1.2 g, 2.79 mmol) and potassium tert-butoxide (469 mg, 4.185 mmol) in N, N-dimethylformamide was heated to 110 C. for 2 hours. As the mixture cooled, 20 ml water was added, and the mixture was extracted with ethyl acetate (350 mL). The combined extracts were washed with brine and concentrated under vacuum to obtain the crude product of the target compound (yellow solid, 900 mg, yield: 71.9%) LCMS(ESI) m/z: 449 (M+1)

Example 36D

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazole-3-carbaldehyde

(191) ##STR00134##

(192) To a mixture of hydrochloride (1.613 g, 44.2 mmol) and water (0.8 g, 44.2 mmol) was added 3-diethoxymethyl-5-((4S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazole (200 mg, 0.446 mmol), and the reaction mixture was heated under reflux for 1 hour. After completion (monitored by LC-MS), the mixture was slowly poured into water and extracted with ethyl acetate (320 mL). The combined extracts were washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum to obtain the crude product of the target compound (yellow solid, 100 mg, yield: 59.9%).

(193) LCMS(ESI) m/z: 393 (M+1)

Example 36E

3-difluoromethyl-5-((4S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazole

(194) ##STR00135##

(195) To a solution of 5-((4S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazol-3-carbaldehyde (100 mg, 0.267 mmol) in anhydrous dichloromethane (10 mL) was added diethylaminosulphur trifluoride (644.72 mg, 1.070 mmol) at 0 C. under an atmosphere of nitrogen, then the reaction mixture was heated to 15 C. and stirred for 10 hours. The mixture was poured into saturated sodium bicarbonate solution and extracted with dichloromethane (315 mL). The combined extracts were washed with brine and concentrated. The crude product was separated by Preparative High Performance Liquid Chromatography to obtain the target compound (15 mg, yield: 14.2%).

(196) .sup.1HNMR (400 MHz, Methanol-d4) ppm 7.65-7.63 (m, 1H), 7.25-7.05 (m, 1H), 7.25-7.22 (m, 2H), 6.84-6.82 (m, 1H), 6.44 (s, 1H), 5.20 (s, 1H), 3.97-3.85 (m, 2H), 2.07-1.98 (m, 3H), 1.97-1.85 (m, 2H), 1.36-1.35 (m, 2H), 1.17-1.14 (m, 3H).

(197) LCMS(ESI) m/z: 397 (M+1)

(198) ##STR00136##

Example 37

2-(5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazol-3-yl)-propan-2-ol

(199) ##STR00137##

Example 37A

Ethyl-2-(5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-formylamino)-2-(hydroxyimino) acetic acid

(200) ##STR00138##

(201) A mixture of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxylic acid (2.0 g, 6.20 mmol) and thionyl chloride (10.0 mL) was heated under reflux for 2 hours and concentrated under reduced pressure to obtain the crude product. To the crude product dissolved in dichloromethane (30 mL) was added a solution of ethyl-2-amino-2-(hydroxyimino) acetic acid (1.0 g, 7.58 mmol) in tetrahydrofuran (30 mL) at 0 C., and the reaction mixture was stirred overnight. After completion, the mixture was concentrated to obtain the target compound (yellow solid, 2.71 g, yield: 100%).

(202) .sup.1HNMR (DMSO-d6, 400 MHz) ppm 7.59 (d, J=7.5 Hz, 1H), 7.24-7.14 (m, 3H), 6.51 (s, 1H), 5.05 (br.s., 1H), 4.33 (q, J=7.2 Hz, 2H), 3.25-2.94 (m, 4H), 2.23-2.12 (m, 1H), 1.97-1.82 (m, 2H), 1.76 (td, J=3.3, 6.5 Hz, 3H), 1.63 (d, J=12.3 Hz, 2H), 1.32 (t, J=7.2 Hz, 3H), 1.03 (t, J=7.3 Hz, 3H).

(203) LCMS (ESI) m/z: 437 (M+1)

Example 37B

Ethyl-5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazole-3-carboxylate

(204) ##STR00139##

(205) To a solution of ethyl-2-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-formylamino)-2-(hydroxyimino)acetic acid (2.71 g, 6.2 mmol) in toluene (250 mL) was added cesium carbonate (4.03 g, 12.4 mmol), and the reaction mixture was stirred at 110 C. for 1 hour. After completion, toluene was concentrated, then water (100 mL) was added to the residue and the mixture was extracted with dichloromethane (3100 mL). The combined extracts were washed with 200 mL brine, dried over anhydrous sodium sulfate and concentrated. The crude product was separated by Preparative High Performance Liquid Chromatography to obtain the target compound (yellow solid, 400 mg, yield: 15%).

(206) .sup.1HNMR (400 MHz, MeOD) ppm 7.51 (d, J=7.0 Hz, 1H), 7.18-7.05 (m, 2H), 6.72 (d, J=8.0 Hz, 1H), 6.32 (s, 1H), 4.53 (q, J=7.0 Hz, 2H), 4.32 (s., 1H), 3.43-3.35 (m, 2H), 3.10 (td, J=7.8, 15.9 Hz, 1H), 2.70-2.58 (m, 3H), 2.10-1.91 (m, 2H), 1.80-1.62 (m, 2H), 1.51 (d, J=13.6 Hz, 1H), 1.46 (t, J=7.3 Hz, 3H), 1.12-1.03 (m, 4H).

(207) LCMS(ESI) m/z: 419 (M+1)

Example 37C

2-(5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazol-3-yl)-propan-2-ol

(208) ##STR00140##

(209) Methylmagnesium bromide (3M, 0.5 mL, 1.5 mmol) was added dropwise to a solution of ethyl-5-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-1,2,4-oxadiazole-3-carboxylate (200 mg, 0.48 mmol) in tetrahydrofuran (5 mL) at 0 C., and the reaction mixture was stirred at 0 C. for 1 hour. After completion, 10 mL water was added to the mixture and the mixture was extracted with dichloromethane (320 mL). The combined extracts were washed with brine, dried over anhydrous sodium sulfate and concentrated. The crude product was separated by Preparative High Performance Liquid Chromatography to obtain the target compound (30 mg, yield: 15.4%).

(210) .sup.1HNMR (400 MHz, MeOD) ppm 7.50 (d, J=7.5 Hz, 1H), 7.20-7.00 (m, 2H), 6.67 (d, J=8.5 Hz, 1H), 6.1 (s, 1H), 4.34 (s., 1H), 3.36 (s., 1H), 3.08 (d, J=8.0 Hz, 1H), 2.77-2.52 (m, 3H), 2.13-1.87 (m, 2H), 1.85-1.61 (m, 9H), 1.51 (d, J=12.0 Hz, 1H), 1.18-1.10 (m, 1H) 1.07 (t, J=7.5 Hz, 3H).

(211) LCMS(ESI) m/z: 405 (M+1)

(212) ##STR00141##

Example 38

(S)-2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyl-4,5-dihydrooxazole

(213) ##STR00142##

Example 38A

(41S,13aS)-13a-ethyl-N((S)-1-hydroxypropan-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide

(214) ##STR00143##

(215) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[,2,1-ij][1,5]naphthyridin-12-carboxylic acid (500 mg, 1.552 mmol) in dichloromethane (7.8 mL) was added O-(7-azabenzotriazole-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (707.7 mg, 1.862 mmol) and diisopropylethylamine (240.25 mg, 1.862 mmol), the mixture was stirred for 1 hour, then L-aminopropanol (233.01 mg, 3.104 mmol) was added and the reaction mixture was stirred for 4 hours. After dilution with water, the reaction mixture was extracted with dichloromethane. The extracts were washed with water and brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified by silica gel column chromatography with dichloromethane/methanol (20/1 by volume) as an eluent to obtain the target compound (570 mg, yield: 96%).

(216) .sup.1HNMR (400 MHz, CHLOROFORM-d) ppm 0.94-1.07 (m, 4H), 1.29 (d, J=7.03 Hz, 3H), 1.36-1.57 (m, 3H), 1.65-1.80 (m, 1H), 1.81-2.00 (m, 2H), 2.52 (d, J=14.05 Hz, 1H), 2.58-2.71 (m, 2H), 2.96-3.10 (m, 1H), 3.19-3.30 (m, 1H), 3.31-3.41 (m, 1H), 3.61-3.70 (m, 1H), 3.80 (d, J=10.54 Hz, 1H), 4.18 (br.s., 1H), 4.30 (br.s., 1H), 5.72 (s, 1H), 6.26 (br.s., 1H), 7.08-7.20 (m, 2H), 7.32 (d, J=8.03 Hz, 1H), 7.46 (d, J=7.53 Hz, 1H).

Example 38B

(S)-2-((41S, 13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyl-4,5-dihydrooxazole

(217) ##STR00144##

(218) A solution of (4.sup.1S,13aS)-13a-ethyl-N((S)-1-hydroxypropan-2-yl)-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-formamide (200 mg, 0.527 mmol) in boron trifluoride diethyl etherate was heated to 120 C. and stirred for 20 hours under an atmosphere of nitrogen. After completion, the reaction mixture was diluted with water, and pH was adjusted to 8 with sodium hydroxide solution. The mixture was extracted with dichloromethane, and the extracts were washed with water and brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (white solid, 60 mg, yield: 31%).

(219) .sup.1HNMR (400 MHz, METHANOL-d4) ppm 7.42 (d, J=8.03 Hz, 1H), 7.25 (d, J=8.03 Hz, 1H), 7.03-7.16 (m, 2H), 5.87 (s, 1H), 4.54-4.67 (m, 1H), 4.43 (dt, J=9.16, 6.71 Hz, 1H), 4.06-4.21 (m, 2H), 3.12-3.31 (m, 2H), 2.88-3.05 (m, 1H), 2.41-2.63 (m, 3H), 1.77-1.97 (m, 2H), 1.58-1.75 (m, 1H), 1.52 (d, J=13.55 Hz, 1H), 1.38 (d, J=6.53 Hz, 4H), 0.86-1.08 (m, 4H).

(220) ##STR00145##

Example 39

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-3-methyl-1,2,4-thiadiazole

(221) ##STR00146##

Example 39A

(41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-thioamide

(222) ##STR00147##

(223) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carbonitrile (2 g, 6.6 mmol) in N,N-dimethylformamide (20 mL) was added ethylsulfamide (1.48 g, 19.8 mmol) and 4 mol/L hydrochloric acid in 1,4-dioxane (8 ml, 33 mmol), respectively, and the reaction mixture was stirred at 120 C. overnight. After cooling, the mixture was adjusted to neutral with aqueous sodium bicarbonate and extracted with ethyl acetate. The extracts were dried and concentrated. The residue was purified by silica gel column chromatography with dichloromethane/tetrahydrofuran (20/1 by volume) as an eluent to obtain the target compound (yellow solid, 580 mg, yield: 26%).

(224) .sup.1HNMR (400 MHz, CHLOROFORM-d) ppm 0.93-1.05 (m, 4H), 1.35-1.42 (m, 1H), 1.55 (d, J=13.80 Hz, 1H), 1.63-1.76 (m, 1H), 1.88-1.95 (m, 2H), 2.47-2.64 (m, 3H), 2.99-3.08 (m, 1H), 3.20-3.30 (m, 1H), 3.32-3.40 (m, 1H), 4.13 (s, 1H), 6.12 (br.s., 1H), 7.08 (br.s., 1H), 7.12-7.20 (m, 2H), 7.35-7.40 (m, 1H), 7.47-7.51 (m, 1H), 7.90 (br.s., 1H).

Example 39B

(41S,13 aS)-N-(1-(dimethylamino)ethylidene)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indol o[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-thioamide

(225) ##STR00148##

(226) A mixture of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-thioamide (560 mg, 1.7 mmol) and N,N-dimethylacetamide dimethyl acetal (3 mL) was stirred at room temperature for 3.5 hours. After evaporation of the solvent, the residue was purified by silica gel column chromatography with dichloromethane/tetrahydrofuran (10/1 by volume) as an eluent to obtain the target compound (orange solid, 800 mg, crude product).

(227) LCMS(ESI) m/z: 407 (M+1)

Example 39C

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-3-methyl-1,2,4-thiadiazole

(228) ##STR00149##

(229) To a solution of (4.sup.1S,13aS)-N-(1-(dimethylamino) ethylidene)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-thioamide (400 mg, 0.98 mmol) in ethanol/methanol (12 ml/6 mL) was added hydroxylamine-O-sulfonic acid (156 mg, 1.4 mmol) and pyridine (311 mg, 3.9 mmol), and the mixture was stirred at 60 C. overnight. After completion, the mixture was diluted with water and extracted with ethyl acetate. The extracts were dried and concentrated. The residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (100 mg, yield: 27%).

(230) .sup.1HNMR (400 MHz, CHLOROFORM-d) ppm 1.12 (t, J=7.15 Hz, 3H), 1.29-1.39 (m, 1H), 1.68-1.86 (m, 2H), 2.21-2.35 (m, 3H), 2.79 (s, 3H), 2.98-3.22 (m, 3H), 3.36 (d, J=6.78 Hz, 1H), 3.63-3.87 (m, 2H), 4.80 (br.s., 1H), 5.77 (s, 1H), 6.51 (d, J=8.28 Hz, 1H), 7.09-7.17 (m, 1H), 7.18-7.25 (m, 1H), 7.53 (d, J=7.78 Hz, 1H).

Example 40

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4,5-dimethylthiazole

(231) ##STR00150##

(232) (4.sup.1S,13aS)-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-thioamide (200 mg, 0.59 mmol) and 3-chloro-2-butanone (9.47 g, 88.89 mmol) were packed into a sealed tube and reacted at 130 C. for 20 hours. After cooling to 20 C., 10 mL ethyl acetate and 20 mL water were added and the aqueous layer was extracted with ethyl acetate (220 mL). The combined extracts were washed with 10 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (40 mg, yield: 15.84%).

(233) .sup.1HNMR (400 MHz, METHANOL-d4) ppm 7.60 (d, J=7.5 Hz, 1H), 7.20-7.15 (m, 1H), 7.13-7.08 (m, 1H), 6.37 (d, J=8.3 Hz, 1H), 5.80 (s, 1H), 5.16 (br.s., 1H), 3.96-3.80 (m, 2H), 3.33-3.12 (m, 4H), 2.55 (s, 3H), 2.44 (s, 3H), 2.09-1.91 (m, 3H), 1.84-1.73 (m, 2H), 1.38-1.28 (m, 1H), 1.12 (t, J=7.2 Hz, 3H).

(234) LCMS(ESI) m/z: 390 (M+1)

(235) ##STR00151##

Example 41

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-methoxy-4-methyloxazole

(236) ##STR00152##

Example 41A

(S)-methyl-2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-formylamino) propionate ethyl

(237) ##STR00153##

(238) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[,2,1-ij][1,5]naphthyridin-12-carboxylic acid (500 mg, 1.552 mmol) in dichloromethane (7.7 mL) was added O-(7-azabenzotriazole-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (707.7 mg, 1.862 mmol) and diisopropylethylamine (600.6 mg, 4.656 mmol), the mixture was stirred for 1 hour, then (S)-alanine methyl ester hydrochloride (431.6 mg, 3.104 mmol) was added and the reaction mixture was stirred for 4 hours. After dilution with water, the reaction mixture was extracted with dichloromethane. The extracts were washed with water and brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified by silica gel column chromatography with dichloromethane/methanol (20/1 by volume) as an eluent to obtain the target compound (white solid, 600 mg, yield: 95%).

(239) LCMS(ESI) m/z: 408 (M+1)

Example 41B

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-methoxy-4-methyloxazole

(240) ##STR00154##

(241) Triethylamine (397.31 mg, 3.93 mmol) was added dropwise to a solution of triphenylphosphine (514.93 mg, 1.96 mmol) and iodine (498.28 mg, 1.96 mmol) in anhydrous dichloromethane (10 mL), the mixture gradually became dark red after stirred for about 10 minutes, a solution of ethyl (S)-methyl-2-((4S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-formylamino)propionate (200 mg, 0.49 mmol) in dichloromethane (2.5 ml) was added and the resulting mixture was stirred for 24 hours until the reaction was completed (monitored by thin layer chromatography). The reaction mixture was diluted with dichloromethane, washed with saturated sodium bicarbonate solution, brine, dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under vacuum. The residue was purified by silica gel column chromatography with petroleum ether/tetrahydrofuran (5/1 by volume) as an eluent to obtain the target compound (40 mg, yield: 20.9%).

(242) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 1.13 (t, J=7.03 Hz, 3H) 1.22-1.35 (m, 1H) 1.79 (br.s., 2H) 1.88-2.09 (m, 3H) 2.11-2.16 (s, 3H) 3.10-3.32 (m, 4H) 3.76-4.01 (m, 5H) 5.13 (br.s., 1H) 5.82 (s, 1H) 6.59 (dd, J=5.77, 2.76 Hz, 1H) 7.20 (dd, J=5.52, 2.51 Hz, 2H) 7.60 (d, J=5.02 Hz, 1H).

(243) ##STR00155##

Example 42

(41S,13aS)-13a-ethyl-12-(imidazo[1,2-a]pyridin-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(244) ##STR00156##

Example 42A

(41S,13aS)-13a-ethyl-N-methoxy-N-methyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide

(245) ##STR00157##

(246) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[,2,1-ij][1,5]naphthyridin-12-carboxylic acid (18 g, 56 mmol) in N,N-dimethylformamide was added N,O-dimethylhydroxylamine hydrochloride (11.3 g, 112 mmol), 0-(7-azabenzotriazole-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (22 g, 56 mmol) and triethylamine (10.6 g, 112 mmol) at room temperature, and the mixture was stirred overnight. After dilution with water, the reaction mixture was extracted with ethyl acetate. The extracts were dried over anhydrous sodium sulfate, filtered and concentrated to obtain the target compound (solid, 18 g, yield: 90%).

(247) LCMS(ESI) m/z: 366 (M+1)

Example 42B

1-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-ethanone

(248) ##STR00158##

(249) Methylmagnesium bromide (50 mL, 150 mmol) was added dropwise to a solution of (4.sup.1S,13aS)-13a-ethyl-N-methoxy-N-methyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide (17 g, 49 mmol) in tetrahydrofuran (170 mL) at 0 C., and the mixture was subsequently stirred at this temperature for 4 hours. The mixture was poured into ammonium chloride solution, extracted with dichloromethane, dried over anhydrous sodium sulfate, filtered and concentrated to obtain the target compound (solid, 11 g, yield: 70.5%).

(250) LCMS(ESI) m/z: 321 (M+1)

Example 42C

2-Bromo-1-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-ethanone

(251) ##STR00159##

(252) To a solution of 1-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-ethanone (7 g, 21.8 mmol) in dichloromethane was added liquid bromine (3.47 g, 21.8 mmol) portionwise and the mixture was stirred at room temperature for 4 hours. The mixture was poured into water and extracted with dichloromethane. The extracts were dried over anhydrous sodium sulfate, filtered and concentrated to give the crude target compound (5 g, yield: 57.6%), which was used directly in the next step.

Example 42D

(41S,13aS)-13a-ethyl-12-(imidazo[1,2-a]pyridin-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(253) ##STR00160##

(254) A mixture of 2-bromo-1-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-ethanone (400 mg, 1 mmol) and 2-aminopyridine (92 mg, 1 mmol) in ethanol (3 mL) was heated to 70 C. and reacted for 8 hours. The resulting solid was filtered out, ethyl acetate was added, and the target compound (100 mg, yield: 25.3%) was isolated by Preparative High Performance Liquid Chromatography.

(255) .sup.1HNMR (CD.sub.3OD, 400 MHz) ppm 8.11 (d, J=6.6 Hz, 1H), 7.69-7.59 (m, 2H), 7.46 (d, J=7.9 Hz, 1H), 7.23 (d, J=7.9 Hz, 1H), 7.04 (t, J=7.5 Hz, 1H), 6.95-6.80 (m, 3H), 6.64 (d, J=8.4 Hz, 1H), 5.60 (s, 1H), 4.31 (br.s., 1H), 3.48-3.27 (m, 2H), 3.15-3.01 (m, 1H), 2.76-2.53 (m, 3H), 2.02-1.86 (m, 2H), 1.60 (d, J=13.7 Hz, 1H), 1.43 (d, J=13.2 Hz, 1H), 1.29-1.15 (m, 1H), 1.01 (t, J=7.5 Hz, 3H).

(256) LCMS(ESI) m/z: 395 (M+1)

Example 43

4-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-thiazole-2-amine

(257) ##STR00161##

(258) A mixture of 2-bromo-1-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-ethanone (400 mg, 1 mmol) and thiourea (92 mg, 1 mmol) in ethanol (3 mL) was heated to 80 C. and reacted for 2 hours. After cooling, the mixture was poured into water and extracted with dichloromethane. The extracts were concentrated, and then the crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (10 mg, yield: 50%).

(259) .sup.1HNMR (CD.sub.3OD, 400 MHz) ppm 7.45 (d, J=7.5 Hz, 1H), 7.10-6.96 (m, 2H), 6.70-6.55 (m, 2H), 5.39 (s, 1H), 5.04 (s, 2H), 4.23 (br.s., 1H), 3.42-3.21 (m, 2H), 3.11-2.98 (m, 1H), 2.70-2.45 (m, 3H), 1.96-1.81 (m, 2H), 1.58-1.34 (m, 2H), 1.18-0.90 (m, 3H).

(260) LCMS(ESI) m/z: 377 (M+1)

Example 44

(41S,13aS)-13a-ethyl-12(7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(261) ##STR00162##

(262) A mixture of 2-bromo-1-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-ethanone (400 mg, 1 mmol) and 2-amino-4-trifluoromethylpyridine (162 mg, 1 mmol) in ethanol (3 mL) was heated under reflux and reacted for 12 hours. Then the mixture was concentrated and the crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (100 mg, yield: 22%).

(263) .sup.1HNMR (CD3OD, 400 MHz) ppm 8.24 (d, J=7.0 Hz, 1H), 7.98 (s, 1H), 7.76 (s, 1H), 7.53-7.43 (m, 1H), 7.10-6.99 (m, 2H), 6.93 (t, J=7.8 Hz, 1H), 6.58 (d, J=8.5 Hz, 1H), 5.64 (s, 1H), 4.31 (br.s., 1H), 3.50-3.28 (m, 2H), 3.17-3.00 (m, 1H), 2.79-2.52 (m, 3H), 2.06-1.72 (m, 4H), 1.49-1.35 (m, 1H), 1.30-1.13 (m, 1H), 1.02 (t, J=7.3 Hz, 3H).

(264) LCMS(ESI) m/z: 463 (M+1)

(265) ##STR00163##

Example 45

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)isoxazole

(266) ##STR00164##

Example 45A

(E)-3-(dimethylamino)-1-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl) prop-2-en-1-one

(267) ##STR00165##

(268) A mixture of 1-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-ethanone (800 mg, 2.5 mmol) and N, N-dimethylformamide dimethyl acetal (8 ml) was heated under reflux and reacted until the starting material disappeared. The target compound (700 mg, yield: 74.7%) for the next step was obtained by decreasing the temperature and concentrating under reduced pressure.

(269) LCMS(ESI) m/z: 376 (M+1)

Example 45B

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)isoxazole

(270) ##STR00166##

(271) To a solution of (E)-3-(dimethylamino)-1-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl) prop-2-en-1-one (350 mg, 0.93 mmol) in N,N-dimethylformamide (3 mL) was added hydroxylamine hydrochloride (100 mg, 1.4 mmol), and the reaction mixture was heated to 120 C. by microwaves and reacted for 2 hours. The mixture was concentrated under vacuum and the residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (60 mg, yield: 18.7%).

(272) .sup.1H NMR (CD.sub.3OD, 400 MHz) ppm 8.53 (s, 1H), 7.48 (d, J=8.0 Hz, 1H), 7.15-6.96 (m, 3H), 6.67 (d, J=8.5 Hz, 1H), 6.45 (s, 1H), 5.58 (s, 1H), 3.07 (br. s., 1H), 2.70 (br. s., 1H), 2.05-1.84 (m, 2H), 1.48 (br. s., 1H), 1.30-1.12 (m, 2H), 1.02 (t, J=7.3 Hz, 3H).

(273) LCMS (ESI) m/z: 346 (M+1)

Example 46

(41S,13aS)-13a-ethyl-12-(1-methyl-1H-pyrazol-3-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine, and

(41S,13aS)-13a-ethyl-12-(1-methyl-1H-pyrazol-5-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine

(274) ##STR00167##

(275) To a solution of (E)-3-(dimethylamino)-1-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl) prop-2-en-1-one (200 mg, 0.53 mmol) in acetic acid (2 mL) was added methylhydrazine (46 mg, 1 mmol). The mixture was refluxed for 4 hours, then poured into water, extracted with dichloromethane, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was subjected to Supercritical Fluid Chromatography to separate and obtain the two target compounds: (4.sup.1S,13aS)-13a-ethyl-12-(1-methyl-1H-pyrazol-3-yl)-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine (20 mg, yield: 10.5%) (.sup.1H NMR (CD.sub.3OD, 400 MHz) ppm 7.51-7.41 (m, 2H), 7.10-6.91 (m, 2H), 6.62 (d, J=8.5 Hz, 1H), 6.30 (d, J=2.0 Hz, 1H), 5.38 (s, 1H), 4.00 (s, 3H), 3.53-3.28 (m, 2H), 3.08 (t, J=15.8 Hz, 1H), 2.84-2.55 (m, 3H), 1.95 (br. s., 2H), 1.61 (d, J=13.1 Hz, 5H), 1.45 (d, J=13.1 Hz, 2H), 1.34-1.11 (m, 2H), 1.02 (t, J=7.3 Hz, 3H), LCMS (ESI) m/z: 359 (M+1)), and, (4.sup.1S,13aS)-13a-ethyl-12-(1-methyl-1H-pyrazol-5-yl)-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine (30 mg, yield: 15.8%) (.sup.1H NMR (CD.sub.3OD, 400 MHz) ppm 7.61 (s, 1H), 7.45 (d, J=7.5 Hz, 1H), 7.11-6.87 (m, 2H), 6.41 (br. s., 1H), 5.89 (d, J=8.5 Hz, 1H), 5.20 (br. s., 1H), 4.37 (br. s., 1H), 3.72-3.27 (m, 5H), 3.14-3.00 (m, 1H), 2.84-2.48 (m, 3H), 2.09-1.93 (m, 1H), 1.86 (dd, J=6.8, 13.8 Hz, 3H), 1.59 (d, J=12.5 Hz, 5H), 1.35-1.15 (m, 3H), 1.02 (t, J=7.3 Hz, 3H), LCMS (ESI) m/z: 359 (M+1)).

Example 47

5-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-3-methylisoxazole

(276) ##STR00168##

(277) A solution of 1-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-ethanone (80 mg, 0.25 mmol) in 2 mL N,N-dimethylacetamide dimethyl acetal was heated under reflux for 2 hours. The low boiling components were removed under vacuum and the residue was dissolved in 5 mL acetonitrile. Then hydroxylamine hydrochloride (20 mg, 0.3 mmol) and phosphorus oxychloride (100 mg) were added, and the reaction mixture was heated under reflux for 1 hour. After cooling to room temperature, the solution was poured into sodium bicarbonate solution, extracted with dichloromethane, washed with brine, dried over anhydrous sodium sulfate, and the solvent was removed under vacuum. The residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound.

(278) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.40 (d, J=7.5 Hz, 1H), 7.08-6.91 (m, 2H), 6.52 (s, 1H), 6.39 (d, J=8.3 Hz, 1H), 5.57 (s, 1H), 4.21 (br. s., 1H), 3.38-3.36 (m, 1H), 3.31-3.15 (m, 2H), 3.07-2.91 (m, 1H), 2.65-2.44 (m, 3H), 2.39 (s, 3H), 2.03 (s, 4H), 1.58-1.34 (m, 2H), 1.00 (t, J=7.4 Hz, 4H).

(279) LCMS (ESI) m/z: 360 (M+1)

(280) ##STR00169##

Example 47

1-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl) butan-1-one-O-methyl oxime

(281) ##STR00170##

Example 48A

1-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)butan-1-one

(282) ##STR00171##

(283) n-propylmagnesium bromide (2M in tetrahydrofuran, 0.825 mL, 1.65 mmol) was slowly added dropwise to a solution of (4.sup.1S,13aS)-13a-ethyl-N-methoxyl-N-methyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide (200 mg, 0.55 mmol) in tetrahydrofuran (2 mL) at 0 C. under an atmosphere of nitrogen, then the reaction mixture was stirred for another 4 hours under this condition. Saturated ammonium chloride solution (20 mL) was added to the mixture, and the mixture was extracted with 40 mL ethyl acetate. The extracts were washed with brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound.

(284) .sup.1H NMR (400 MHz, MeOD) ppm 7.52-7.61 (m, 1H), 7.16-7.28 (m, 2H), 7.00-7.06 (m, 1H), 6.30 (s, 1H), 3.58-3.77 (m, 2H), 3.23-3.30 (m, 1H), 3.11-3.23 (m, 2H), 2.98-3.08 (m, 1H), 2.84-2.96 (m, 2H), 2.01-2.15 (m, 1H), 1.94 (dt, J=14.68, 7.47 Hz, 2H), 1.70-1.88 (m, 4H), 1.03-1.24 (m, 7H).

(285) LCMS (ESI) m/z: 349 (M+1)

Example 48B

1-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)butan-1-one-O-methyl oxime

(286) ##STR00172##

(287) A mixture of 1-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)butan-1-one (200 mg, 0.55 mmol), methoxylamine hydrochloride (455 mg, 5.5 mmol), sodium acetate (445 mg, 5.5 mmol) and ethanol (10 mL) was refluxed overnight. The mixture was diluted with water (20 mL) and extracted with 40 mL dichloromethane. The extracts were washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by Preparative High Performance Liquid Chromatography and Supercritical Fluid Chromatography to obtain the target compound.

(288) Supercritical Fluid Chromatography:

(289) column: Chiralpak AD-H 2504.6 mm I.D., 5 um; mobile phase: isopropanol (0.05% DEA), CO.sub.2 5%-40%; flow rate: 2.35 mL/min; wavelength: 220 nm

(290) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 7.55 (d, J=7.53 Hz, 1H), 7.11-7.24 (m, 3H), 5.28 (s, 1H), 4.01 (s, 3H), 3.64-3.79 (m, 2H), 2.95-3.25 (m, 5H), 2.23 (s, 1H), 1.97-2.12 (m, 2H), 1.77-1.97 (m, 2H), 1.67 (d, J=11.04 Hz, 2H), 1.51 (dt, J=15.18, 7.72 Hz, 2H), 1.42 (s, 3H), 1.17-1.33 (m, 2H), 1.10 (t, J=7.53 Hz, 3H), 0.91 (t, J=7.28 Hz, 3H).

(291) LCMS (ESI) m/z: 378 (M+1)

Example 49

4-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl) heptan-4-ol

(292) ##STR00173##

(293) n-propylmagnesium bromide (2M in tetrahydrofuran, 2.14 mL, 4.29 mmol) was slowly added dropwise to a solution of vinpocetine (300 mg, 0.86 mmol) in tetrahydrofuran (2 mL) at 0 C. under an atmosphere of nitrogen, then the mixture was stirred for another 4 hours under such condition. Saturated ammonium chloride solution (20 mL) was added into the mixture, and the mixture was extracted with 40 mL ethyl acetate. The extracts were washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound.

(294) .sup.1H NMR (400 MHz, MeOD) ppm 8.51-8.63 (m, 1H), 7.34-7.44 (m, 1H), 7.00-7.14 (m, 2H), 5.30 (s, 1H), 4.09 (br. s., 1H), 3.20-3.31 (m, 2H), 2.99-3.13 (m, 1H), 2.52-2.71 (m, 3H), 1.95 (br. s., 4H), 1.43 (br. s., 8H), 0.96-1.14 (m, 8H), 0.72 (t, J=7.28 Hz, 3H).

(295) LCMS (ESI) m/z: 393 (M+1)

(296) ##STR00174##

Example 50

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole

(297) ##STR00175##

Example 50A

(41S,13aS)-13a-ethyl-N((S)-1-(methoxyl(methyl)amino)-1-oxopropan-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide

(298) ##STR00176##

(299) Oxalyl chloride (590.98 mg, 4.656 mmol) was added dropwise to a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxylic acid (500 mg, 1.552 mmol) and a catalytic amount of N,N-dimethylformamide (0.075 mL) in anhydrous dichloromethane (7.5 mL) at 0 C. and the reaction mixture was stirred at this temperature for another 1 hour. The solvent was removed under reduced pressure, and the resulting crude product was immediately dissolved in dichloromethane (7.5 mL). Then diisopropylethylamine (600.61 mg, 4.656 mmol) and (S)-2-amino-N-methoxy-N-methylpropanamide (307.5 mg, 2.328 mmol) were added, the reaction mixture was stirred at room temperature for 2 hours. Water was added and the mixture was extracted with dichloromethane. The extracts were washed with water, brine, dried over anhydrous sodium sulfate and the solvent was concentrated under vacuum. The residue was purified by silica gel column chromatography with dichloromethane/methanol (20/1 by volume) as an eluent to obtain the target compound (white solid, 460 mg, yield: 68%).

(300) LCMS (ESI) m/z: 437 (M+1)

Example 50B

(41S,13aS)-13a-ethyl-N((S)-1-oxopropan-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide

(301) ##STR00177##

(302) To a solution of (4.sup.1S,13aS)-13a-ethyl-N((S)-1-(methoxyl(methyl)amino)-1-oxopropan-2-yl)-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide in tetrahydrofuran was added lithium aluminium hydride (32.66 mg, 0.86 mmol) at 78 C. under an atmosphere of nitrogen, then the dry ice-acetone bath was replaced by an ice bath, the reaction temperature was increased to 0 C. After the reaction mixture was stirred for 20 minutes, the reaction temperature was decreased to 78 C. again, then the reaction was rapidly quenched by adding potassium bisulfate solution. After the temperature of the mixture was increased to room temperature, the solid was filtered out, and the filtrate was extracted with ethyl acetate. The combined extracts were washed with brine, dried over anhydrous sodium sulfate, filtered and the solvent was removed to obtain the crude target compound (for the next step, 190 mg, yield: 88%).

(303) LCMS (ESI) m/z: 378 (M+1)

Example 50C

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole

(304) ##STR00178##

(305) To a solution of (4.sup.1S,13aS)-13a-ethyl-N((S)-1-oxopropan-2-yl)-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide (190 mg, 0.504 mmol) in anhydrous acetonitrile (5 mL) was added a catalytic amount of N,N-dimethylformamide (0.025 mL) and phosphorus oxychloride (386.59 mg, 2.518 mmol), then the reaction mixture was heated to 90 C. and stirred under an atmosphere of nitrogen for 3 hours. After completion, the reaction solution was poured into a sodium carbonate solution and pH was adjusted to 8, then the mixture was extracted with dichloromethane. The combined extracts were washed with water, brine, dried over anhydrous sodium sulfate, and the solvent was removed under vacuum. The crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (30 mg, yield: 32%).

(306) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 1.13 (t, J=6.27 Hz, 3H), 1.24-1.47 (m, 2H), 1.70-1.86 (m, 2H), 1.91-2.14 (m, 3H), 2.30 (s, 3H), 2.72 (s, 2H), 3.11-3.22 (m, 1H), 3.78-3.96 (m, 2H), 5.14 (br. s., 1H), 5.90 (s, 1H), 6.45 (d, J=8.03 Hz, 1H), 7.08-7.24 (m, 2H), 7.60 (d, J=7.03 Hz, 1H), 7.87 (s, 1H).

(307) LCMS (ESI) m/z: 360 (M+1)

(308) ##STR00179##

Example 51

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-methyloxazole

(309) ##STR00180##

Example 51A

(41S,13aS)-13a-ethyl-N-(2-oxopropyl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrid o[3,2,1-ij][1,5]naphthyridin-12-carboxamide

(310) ##STR00181##

(311) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxylic acid (200 mg, 0.621 mmol) in dichloromethane (3.1 mL) was added O-(7-azabenzotriazole-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (283.08 mg, 0.745 mmol) and diisopropylethylamine (240.25 mg, 1.862 mmol) and the mixture was stirred for 1 hour. Then aminopropanone hydrochloride (135.37 mg, 1.242 mmol) was added and the mixture was stirred for another 4 hours. Water was added to the mixture, and the mixture was extracted with dichloromethane. The combined extracts were washed with water, brine and dried over anhydrous sodium sulfate. The organic layer was concentrated under vacuum and the residue was purified by silica gel column chromatography with dichloromethane/methanol (20/1 by volume) as an eluent to obtain the target compound (white solid, 210 mg, yield: 89%).

(312) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 0.98-1.15 (m, 4H), 1.50-1.55 (m, 1H), 1.59 (d, J=13.55 Hz, 1H), 1.81-2.11 (m, 3H), 2.30 (s, 3H), 2.62-2.93 (m, 3H), 3.00-3.15 (m, 1H), 3.31-3.43 (m, 1H), 3.44-3.56 (m, 1H), 4.27-4.40 (m, 2H), 4.43-4.54 (m, 1H), 5.69-5.75 (m, 1H), 6.78 (br. s., 1H), 7.16 (quin, J=6.71 Hz, 2H), 7.21-7.26 (m, 1H), 7.47 (d, J=7.03 Hz, 1H).

Example 51B

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-methyloxazole

(313) ##STR00182##

(314) To a solution of (4.sup.1S,13aS)-13a-ethyl-N-(2-oxopropyl)-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide (210 mg, 0.557 mmol) in anhydrous acetonitrile (2.8 mL) was added a catalytic amount of N,N-dimethylformamide (0.028 mL) and phosphorus oxychloride (854.56 mg, 5.567 mmol), then the reaction mixture was heated to 90 C. and stirred under an atmosphere of nitrogen for 3 hours. After completion, the reaction solution was poured into a sodium carbonate solution and the pH was adjusted to 8, then the mixture was extracted with dichloromethane. The combined extracts were washed with water, brine, dried over anhydrous sodium sulfate, and the solvent was removed under vacuum. The crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (50 mg, yield: 25%).

(315) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 1.12 (t, J=6.78 Hz, 3H), 1.23-1.36 (m, 1H), 1.79 (t, J=12.55 Hz, 2H), 1.90-2.12 (m, 3H), 2.45 (s, 3H), 3.12 (d, J=16.06 Hz, 1H), 3.25 (d, J=12.05 Hz, 2H), 3.37 (s, 1H), 3.75-4.00 (m, 2H), 5.14 (br. s., 1H), 5.88 (s, 1H), 6.53 (d, J=8.03 Hz, 1H), 7.05-7.26 (m, 3H), 7.60 (d, J=7.03 Hz, 1H).

Example 52

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4,5-dimethyloxazole

(316) ##STR00183##

(317) The process of the example was the same as that of Example 51.

(318) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 1.09 (t, J=7.40 Hz, 3H), 1.24 (td, J=13.93, 3.26 Hz, 1H), 1.63 (d, J=14.56 Hz, 1H), 1.73 (d, J=14.05 Hz, 1H), 2.08-2.26 (m, 6H), 2.32 (s, 3H), 2.90-3.07 (m, 2H), 3.08-3.20 (m, 1H), 3.26 (d, J=11.04 Hz, 1H), 3.64 (td, J=12.67, 5.77 Hz, 1H), 3.73-3.84 (m, 1H), 4.73 (br. s., 1H), 5.79 (s, 1H), 6.56-6.64 (m, 1H), 7.11-7.22 (m, 2H), 7.46-7.55 (m, 1H).

Example 53

5-ethyl-2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole

(319) ##STR00184##

(320) The process of the example was the same as that of Example 51.

(321) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 1.11 (t, J=7.28 Hz, 3H), 1.17-1.34 (m, 4H), 1.60-1.81 (m, 2H), 2.14-2.38 (m, 6H), 2.58-2.78 (m, 2H), 2.91-3.22 (m, 3H), 3.31 (d, J=10.04 Hz, 1H), 3.65 (br. s., 1H), 3.80 (d, J=11.04 Hz, 1H), 4.76 (br. s., 1H), 5.83 (s, 1H), 6.52 (d, J=8.03 Hz, 1H), 7.17 (quin, J=7.03 Hz, 2H), 7.50 (d, J=7.03 Hz, 1H), 13.07 (br. s., 1H).

Example 54

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-isopropyl-4-methyloxazole

(322) ##STR00185##

(323) The process of the example was the same as that of Example 51.

(324) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 1.12 (t, J=7.03 Hz, 3H), 1.18-1.35 (m, 7H), 1.66 (d, J=14.05 Hz, 1H), 1.79 (d, J=14.05 Hz, 1H), 2.13-2.38 (m, 6H), 2.94-3.23 (m, 4H), 3.32 (d, J=9.54 Hz, 1H), 3.66 (br. s., 1H), 3.80 (d, J=10.54 Hz, 1H), 4.78 (br. s., 1H), 5.91 (s, 1H), 6.43 (d, J=8.03 Hz, 1H), 7.10-7.24 (m, 2H), 7.51 (d, J=7.53 Hz, 1H).

Example 55

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4,5,6,7-tetrahydrobenzo[d]oxazole

(325) ##STR00186##

(326) The process of the example was the same as that of Example 51.

(327) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 7.52 (dd, J=6.27, 2.76 Hz, 1H), 7.15-7.25 (m, 2H), 6.65-6.76 (m, 1H), 5.91 (s, 1H), 4.77 (br. s., 1H), 3.81 (d, J=11.29 Hz, 1H), 3.33 (d, J=9.79 Hz, 1H), 3.15 (br. s., 1H), 3.02 (d, J=10.54 Hz, 1H), 2.58-2.77 (m, 4H), 2.17-2.39 (m, 4H), 1.87-2.05 (m, 4H), 1.80 (d, J=14.05 Hz, 1H), 1.68 (d, J=14.31 Hz, 1H), 1.21-1.38 (m, 1H), 1.13 (t, J=7.28 Hz, 3H).

Example 56

4-ethyl-2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-5-methyloxazole

(328) ##STR00187##

(329) The process of the example was the same as that of Example 51.

(330) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 1.06-1.17 (m, 3H), 1.28 (t, J=7.53 Hz, 4H), 1.70-1.84 (m, 2H), 1.91-2.15 (m, 4H), 2.38 (s, 3H), 2.54-2.65 (m, 2H), 3.09-3.30 (m, 3H), 3.76-3.96 (m, 2H), 5.12 (br. s., 1H), 5.85 (s, 1H), 6.54 (d, J=7.53 Hz, 1H), 7.16 (quin, J=7.03 Hz, 2H), 7.59 (d, J=7.53 Hz, 1H).

Example 57

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-isopropyl-5-methyloxazole

(331) ##STR00188##

(332) The process of the example was the same as that of Example 51.

(333) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 1.13 (t, J=7.28 Hz, 3H), 1.29 (dd, J=9.91, 6.90 Hz, 7H), 1.70-1.83 (m, 2H), 1.92-2.14 (m, 3H), 2.38 (s, 3H), 2.96-3.07 (m, 1H), 3.10-3.35 (m, 5H), 3.74-3.96 (m, 2H), 5.12 (br. s., 1H), 5.84 (s, 1H), 6.53 (d, J=7.78 Hz, 1H), 7.09-7.21 (m, 2H), 7.58 (d, J=7.53 Hz, 1H).

(334) ##STR00189##

Example 58

5-cyclopropyl-2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrid o[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole

(335) ##STR00190##

Example 58A

(S)-2-amino-N-methoxy-N-methylpropanamide hydrochloride

(336) ##STR00191##

(337) (S)-tert-butyl-(1-(methoxyl(methyl)amino)-1-oxopropyl-2-yl)carbamate (20.0 g, 106.82 mmol) was dissolved in 4M ethyl acetate hydrochloride (100 mL) and the mixture was stirred at 20 C. for 2 hours. The target compound (12.0 g, yield: 90.9%) was obtained by removing the low boiling components.

(338) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 1.54-1.71 (m, 3H), 3.23 (s, 1H), 3.82 (s, 1H), 3.93-4.28 (m, 2H), 4.53 (br. s., 1H), 8.39 (br. s., 3H).

Example 58B

(41S,13aS)-13a-ethyl-N((S)-1-(methoxyl(methyl)amino)-1-oxopropyl-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide

(339) ##STR00192##

(340) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxylic acid (5.0 mg, 15.51 mmol) in dichloromethane (80 mL) was added O-(7-azabenzotriazole-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (7.08 g, 18.61 mmol) and N,N-diisopropylethylamine (3.01 g, 23.26 mmol) and the mixture was stirred at 20 C. for 1 hour. Then N,N-diisopropylethylamine (4.01 g, 31.02 mmol) and (S)-2-amino-N-methoxy-N-methylpropionamide hydrochloride (2.11 g, 17.06 mmol) were added and the mixture was stirred for another 14 hours. Water was added to the mixture, and the mixture was extracted with dichloromethane (310 mL). The combined extracts were washed with water (10 mL), brine (10 mL) and dried over anhydrous sodium sulfate. The solvent was removed under vacuum and the residue was purified by silica gel column chromatography with dichloromethane/methanol (20/1 by volume) as an eluent to obtain the target compound (light yellow gum, 5.5 g, yield: 90.58%).

(341) LCMS (ESI) m/z: 437 (M+1)

Example 58C

(41S,13aS)-N((S)-1-cyclopropyl-1-oxopropyl-2-yl)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide

(342) ##STR00193##

(343) Cyclopropylmagnesium bromide (0.5 M, 307.8 mL, 153.9 mmol) was directly added dropwise to the solid (4.sup.1S,13aS)-13a-ethyl-N((S)-1-(methoxyl(methyl)amino)-1-oxopropyl-2-yl)-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide (2.24 g, 5.13 mmol) at 0 C. over a period of more than 60 minutes. After completion, the reaction mixture was heated to 20 C. and stirred for another 18 hours. Then the reaction temperature was decreased to 0 C., and saturated ammonium chloride solution was added, the mixture was extracted with ethyl acetate (330 mL). The combined extracts were washed with water (30 mL), brine (30 mL), dried over anhydrous sodium sulfate, and the solvent was removed under vacuum. The residue was purified by silica gel column chromatography with dichloromethane/methanol (20/1 by volume) as an eluant to obtain the target compound (light yellow gum, 1.7 g, yield: 79.37%).

(344) LCMS (ESI) m/z: 418 (M+1)

Example 58D

5-cyclopropyl-2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrid o[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole

(345) ##STR00194##

(346) To a solution of (4.sup.1S,13aS)-N((S)-1-cyclopropyl-1-oxopropyl-2-yl)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide (200 mg, 0.479 mmol) in anhydrous acetonitrile (2.8 mL) was added a catalytic amount of N,N-dimethylformamide (17.5 mg) and phosphorus oxychloride (367.22 mg, 2.39 mmol), then the reaction mixture was heated to 90 C. and stirred under an atmosphere of nitrogen for 15 hours. After completion, the reaction solution was poured into a sodium carbonate solution and the pH was adjusted to 8, then the mixture was extracted with dichloromethane (310 mL). The combined extracts were washed with water (10 mL), brine (10 mL), dried over anhydrous sodium sulfate, and the solvent was removed under vacuum. The residue was purified by silica gel column chromatography with petroleum ether/tetrahydrofuran (5/1 by volume) as an eluent to obtain the target compound (light yellow solid, 100 mg, yield: 52.25%).

(347) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 0.71-0.88 (m, 2H), 0.91-1.03 (m, 2H), 1.12 (t, J=7.28 Hz, 3H), 1.27 (td, J=13.99, 2.89 Hz, 1H), 1.67 (d, J=14.05 Hz, 1H), 1.78 (d, J=14.31 Hz, 1H), 1.86-1.96 (m, 1H), 2.15-2.34 (m, 6H), 2.93-3.25 (m, 3H), 3.32 (d, J=10.29 Hz, 1H), 3.65 (br. s., 1H), 3.81 (d, J=11.29 Hz, 1H), 4.76 (br. s., 1H), 5.82 (s, 1H), 6.45-6.54 (m, 1H), 7.14-7.24 (m, 2H), 7.47-7.56 (m, 1H).

(348) ##STR00195##

Example 59

2-(2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazol-5-yl)propan-2-ol

(349) ##STR00196##

Example 59A

(41S,13aS)-3-amino-1-methoxyl-1-oxobut-2-en-2-yl-13a-ethyl-2,3,41,5,6,13a-hexahydro-1 H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carbonate

(350) ##STR00197##

(351) To a mixture of methyl 3-aminocrotonate (1.5 g, 13.03 mmol) and iodosobenzene (3.44 g, 15.63 mmol) in dichloroethane (75 mL) was added (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxyl acid (5.04 g, 15.63 mmol) at 20 C. and the reaction mixture was stirred at such temperature for 20 hours. The reaction was quenched with saturated sodium bicarbonate solution (150 mL), and the mixture was extracted with dichloromethane (3100 mL). The combined extracts were dried over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by silica gel column chromatography with tetrahydrofuran/petroleum ether (1/10-1/2 by volume) as an eluent to obtain the target compound (white solid, 1.5 g, yield: 26.4%).

(352) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 7.49-7.44 (m, 1H), 7.40-7.34 (m, 1H), 7.18-7.09 (m, 2H), 6.39 (br. s., 1H), 4.21 (br. s., 1H), 3.85-3.68 (m, 3H), 3.40-3.33 (m, 1H), 3.32-3.21 (m, 1H), 3.10-2.98 (m, 1H), 2.68-2.61 (m, 2H), 2.52 (dd, J=2.9, 16.2 Hz, 1H), 2.02 (br. s., 3H), 1.87-1.72 (m, 2H), 1.52 (br. s., 1H), 1.47-1.40 (m, 1H), 1.12-0.98 (m, 5H).

Example 59B

Methyl-2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole-5-carbonate

(353) ##STR00198##

(354) (4.sup.1S,13aS)-3-amino-1-methoxyl-1-oxobut-2-en-2-yl-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carbonate (1.5 g, 3.44 mmol) was added to acetic acid (20 mL), the mixture was heated to 120 C. and stirred for 20 hours. The solvent was distilled off, dichloromethane (50 mL) and water (30 mL) were added to the residue, and the separated aqueous layer was extracted with dichloromethane (250 mL). The combined organic phases were washed with 30 mL of brine, dried over sodium sulfate, filtered and the filtrate was concentrated. The crude product was purified by silica gel column chromatography with tetrahydrofuran/petroleum ether (0-2/5 by volume) as an eluent to obtain the target compound (580 mg, yield: 40.38%).

(355) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.61 (dd, J=2.0, 6.5 Hz, 1H), 7.25-7.13 (m, 2H), 6.79-6.67 (m, 1H), 6.12 (s, 1H), 5.13 (s, 1H), 3.97-3.79 (m, 5H), 3.37-3.34 (m, 0.5H), 3.32-3.13 (m, 3.5H), 2.56 (s, 3H), 2.08-1.91 (m, 3H), 1.87-1.74 (m, 2H), 1.35-1.24 (m, 1H), 1.13 (t, J=7.3 Hz, 3H).

(356) LCMS (ESI) m/z: 418 (M+1)

Example 60

2-(2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazol-5-yl)propan-2-ol

(357) ##STR00199##

(358) To a solution of methyl-2-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazol-5-carbonate (100 mg, 0.24 mmol) in anhydrous tetrahydrofuran (2 mL) was added methylmagnesium bromide (3M, 0.4 mL, 1.2 mmol) at 70 C. under an atmosphere of nitrogen, and the reaction mixture was stirred at 70 to 20 C. for 16 hours. The reaction was quenched with 2 mL saturated ammonium chloride solution at 78 to 0 C., and the mixture was extracted with ethyl acetate (310 mL). The combined extracts were washed with brine (10 mL), dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated. The residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (52.0 mg, yield: 52.0%).

(359) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.59 (d, J=7.3 Hz, 1H), 7.24-7.08 (m, 2H), 6.42 (d, J=7.8 Hz, 1H), 5.86 (s, 1H), 5.14 (br. s., 1H), 3.96-3.77 (m, 2H), 3.38-3.07 (m, 4H), 2.40 (s, 3H), 2.09-1.91 (m, 3H), 1.86-1.72 (m, 2H), 1.53 (d, J=14.1 Hz, 6H), 1.35-1.25 (m, 1H), 1.12 (t, J=7.0 Hz, 3H).

(360) LCMS (ESI) m/z: 418 (M+1)

Example 61

(2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazol-5-yl)methanol

(361) ##STR00200##

(362) To a solution of methyl-2-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole-5-carbonate (100 mg, 0.24 mmol) in anhydrous dichloromethane (8 mL) was added dibutyl aluminium hydride (1 M, 0.527 mL, 0.527 mmol) at 70 C., and the reaction mixture was stirred at 70 to 15 C. for 2 hours. The reaction was quenched by slow addition of saturated ammonium chloride (5 mL) at 78 to 0 C. and the mixture was extracted with ethyl acetate (330 mL). The combined extracts were washed with brine (20 mL), dried over sodium sulfate, filtered and the filtrate was concentrated. The crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (50.0 mg, yield: 53.6%).

(363) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.60 (d, J=7.5 Hz, 1H), 7.24-7.12 (m, 2H), 6.60 (d, J=7.8 Hz, 1H), 5.93 (s, 1H), 5.14 (br. s., 1H), 4.64 (s, 2H), 3.99-3.74 (m, 2H), 3.36-3.09 (m, 4H), 2.31 (s, 3H), 2.10-1.91 (m, 3H), 1.86-1.73 (m, 2H), 1.35-1.24 (m, 1H), 1.13 (t, J=7.0 Hz, 3H).

(364) LCMS (ESI) m/z: 390 (M+1)

(365) ##STR00201## ##STR00202##

Example 62

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole-5-carbonitrile

(366) ##STR00203##

Example 62A

2-((4 is, 3aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole-5-carboxylic acid

(367) ##STR00204##

(368) A solution of sodium hydroxide (330.0 mg, 8.25 mmol) in water (10 mL) was added dropwise to a solution of methyl-2-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazol-5-carbonate (1.80 g, 4.31 mmol) in methanol (10 mL) under stirring, and the mixture was stirred for about 16 hours. After completion, the low boiling components were distilled off and the residue was washed with ethyl acetate (330 ml). The aqueous phase was acidified with 6M hydrochloric acid. After being filtered, the precipitated solid (filter cake) was washed with water (320 mL), dissolved in methanol (20 mL), dried over anhydrous sodium sulfate, filtered and concentrated to obtain the target compound (1.20 g, yield: 69.01%).

(369) LCMS (ESI) m/z: 404 (M+1)

Example 62B

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole-5-carboxamide

(370) ##STR00205##

(371) To a solution of 2-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazol-5-carboxylic acid (100 mg, 0.248 mmol), 1-hydroxybenzotriazole (50 mg, 0.372 mmol) and 1-(3-dimethyllaminopropyl)-3-ethyl-carbodiimide hydrochloride (71 mg, 0.372 mmol) in N,N-dimethylformamide (5 mL) was added triethylamine (75 mg, 0.744 mmol) and ammonium chloride (40 mg, 0.744 mmol), respectively, and the reaction mixture was stirred for about 16 hours. After completion, the mixture was poured into water (with a volume of 5 times) and extracted with ethyl acetate (530 mL). The combined extracts were dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (white solid, 50 mg, yield: 50.12%).

(372) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.72-7.55 (m, 1H), 7.31-7.13 (m, 2H), 6.83-6.59 (m, 1H), 6.18 (s, 1H), 5.14 (br. s., 1H), 3.99-3.76 (m, 2H), 3.30-3.09 (m, 3H), 2.56 (s, 3H), 2.19-1.93 (m, 3H), 1.88-1.65 (m, 2H), 1.43-1.25 (m, 1H), 1.16 (t, J=7.3 Hz, 3H).

(373) LCMS (ESI) m/z: 403 (M+1)

Example 63

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole-5-carbonitrile

(374) ##STR00206##

(375) To a solution of 2-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole-5-carboxamide (150 mg) in chloroform (10 mL) was added phosphorus oxychloride (571 mg, 3.73 mmol) under stirring, the reaction mixture was heated to 50 C. and stirred for 6 hours. After cooling, the mixture was carefully poured into water (10 mL), the pH was adjusted to 7-8 with saturated sodium bicarbonate solution, and the mixture was extracted with dichloromethane (320 mL). The combined extracts were concentrated and the residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (80 mg, yield: 55.83%).

(376) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.63 (dd, J=2.5, 6.3 Hz, 1H), 7.32-7.18 (m, 2H), 6.90-6.70 (m, 1H), 6.19 (s, 1H), 5.15 (br. s., 1H), 4.07-3.78 (m, 2H), 3.32-3.13 (m, 4H), 2.47 (s, 3H), 2.13-1.92 (m, 3H), 1.88-1.71 (m, 2H), 1.40-1.24 (m, 1H), 1.14 (t, J=7.3 Hz, 3H).

(377) LCMS (ESI) m/z: 385 (M+1)

Example 64

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-N,4-dimethyloxazole-5-carboxamide

(378) ##STR00207##

(379) To a solution of 2-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole-5-carboxylic acid (100 mg, 0.248 mmol), 1-hydroxylbenzotriazole (50 mg, 0.37 mmol) and 1-(3-dimethyllaminopropyl)-3-ethyl-carbodiimide hydrochloride (72 mg, 0.376 mmol) in N,N-dimethylformamide (5 mL) was added triethylamine (75 mg, 0.744 mmol) and a solution of methylamine in tetrahydrofuran (1 M, 0.74 mL, 0.74 mmol), respectively, and the reaction mixture was stirred for about 16 hours. After completion, the mixture was poured into water with a volume of 5 times and extracted with ethyl acetate (530 mL). The combined extracts were dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (20 mg, yield: 19.37%).

(380) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.78-7.54 (m, 1H), 7.30-7.16 (m, 2H), 6.87-6.65 (m, 1H), 6.16 (s, 1H), 5.15 (br. s., 1H), 4.08-3.77 (m, 2H), 3.31-3.23 (m, 2H), 3.21 (d, J=5.0 Hz, 1H), 2.87 (s, 3H), 2.57 (s, 3H), 2.01 (dd, J=7.5, 10.0 Hz, 3H), 1.82 (br. s., 2H), 1.32 (br. s., 1H), 1.16 (t, J=7.5 Hz, 3H).

(381) LCMS (ESI) m/z: 417 (M+1)

Example 65

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-N,N,4-trimethyloxazole-5-carboxamide

(382) ##STR00208##

(383) To a solution of 2-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazole-5-carboxylic acid (100 mg, 0.248 mmol), 1-hydroxylbenzotriazole (50 mg, 0.37 mmol) and 1-(3-dimethyllaminopropyl)-3-ethyl-carbodiimide hydrochloride (72 mg, 0.376 mmol) in N,N-dimethylformamide (5 mL) was added triethylamine (75 mg, 0.744 mmol) and dimethylamine hydrochloride (60 ml, 0.744 mmol), respectively, and the reaction mixture was stirred for about 16 hours. After completion, the mixture was poured into water with a volume of 5 times and extracted with ethyl acetate (530 mL). The combined extracts were dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (50 mg, yield: 46.86%).

(384) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.75-7.55 (m, 1H), 7.32-7.10 (m, 2H), 6.76-6.51 (m, 1H), 6.07 (s, 1H), 5.18 (br. s., 1H), 4.03-3.76 (m, 2H), 3.30-3.16 (m, 2H), 3.16-2.96 (m, 6H), 2.48 (s, 3H), 2.15-1.90 (m, 3H), 1.82 (br. s., 2H), 1.32 (br. s., 1H), 1.15 (t, J=7.3 Hz, 3H).

(385) LCMS (ESI) m/z: 431 (M+1)

(386) ##STR00209##

Example 66

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-6,7-dihydro-4H-pyrano[3,4-d]oxazole

(387) ##STR00210##

Example 66A

4,4-dimethoxytetrahydro-2H-pyran-3-ol

(388) ##STR00211##

(389) To a solution of potassium hydroxide (15.82 g, 240 mmol) in 210 mL of methanol was added tetrahydropyran-4-one (10 g, 99.88 mmol) at 0-5 C. After about 5-10 minutes, a solution of iodine (27.89 g, 109.87 mmol) dissolved in 185 ml methanol was added dropwise over a period of more than 1.5 hours, then the mixture was gradually heated to room temperature. The mixture was concentrated, 50 mL toluene was added and the mixture was filtered. The filtrate was distilled off and the residue was purified by silica gel column chromatography with petroleum ether/ethyl acetate (1/1 by volume) as an eluent to obtain the target compound (yellow liquid, 10.0 g, yield: 61.73%)

(390) .sup.1H NMR (400 MHz, CDCl3-d) ppm 4.13 (q, J=7.03 Hz, 1H), 3.77-3.90 (m, 2H), 3.65-3.74 (m, 2H), 3.50 (td, J=11.67, 2.51 Hz, 1H), 3.27 (d, J=7.28 Hz, 6H), 2.31 (br. s., 1H), 2.05 (s, 1H), 1.95 (ddd, J=14.31, 11.80, 4.77 Hz, 1H), 1.71-1.83 (m, 2H), 1.27 (t, J=7.03 Hz, 1H).

Example 66B

4,4-dimethoxy-dihydro-2H-pyran-3(4H)-one

(391) ##STR00212##

(392) To a solution of 4,4-dimethoxytetrahydro-2H-pyran-3-ol (2.0 g, 12.33 mmol) in dichloromethane (30 mL) was added 4 molecular sieve (5.0 g, 12.33 mmol), N-methyl morpholine-N-oxide (3.64 g, 31.08 mmol) and tetrapropyl perruthenate (200 mg, 0.569 mmol), and the reaction mixture was stirred for about 30 minutes. After filtration, the filtrate was concentrated, and the residue was purified by silica gel column chromatography with petroleum ether/ethyl acetate (10/1 by volume) as an eluent to obtain the target compound (yellow liquid, 1.2 g, yield: 60.76%).

(393) .sup.1H NMR (400 MHz, CDCl3-d) ppm 4.05 (s, 2H), 3.90-3.98 (m, 2H), 3.66-3.72 (m, 1H), 3.19-3.27 (m, 6H), 2.27 (s, 1H), 2.16-2.23 (m, 2H).

Example 66C

4,4-dimethoxy-tetrahydro-2H-pyran-3-amine

(394) ##STR00213##

(395) To a solution of 4,4-dimethoxy-dihydro-2H-pyran-3(4H)-one (1.2 g, 7.49 mmol) in methanol (30 mL) was added palladium on carbon (50 mg) and formamide (4.72 g, 74.9 mmol) at 20 C. under an atmosphere of nitrogen, respectively, and the mixture was stirred at 20 C. overnight. The reaction mixture was filtered and the filtrate was concentrated to obtain the crude target compound (for the next step, 800 mg).

Example 66D

(41S,13aS)-N-(4,4-dimethoxy-tetrahydro-2H-pyran-3-yl)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide

(396) ##STR00214##

(397) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxylic acid (300 mg, 0.93 mmol) in dichloromethane (20 mL) was added two drops of N,N-dimethylformamide at 0 C., then oxalyl chloride (236.22 mg, 1.86 mmol) was slowly added dropwise thereto, and the reaction mixture was stirred at 0 C. under an atmosphere of nitrogen for 1 hour. After the mixture was concentrated under vacuum, the residue was dissolved in dichloromethane (20 mL), and then diisopropylethylamine (240.52 mg, 1.86 mmol) and 4,4-dimethoxy-tetrahydro-2H-pyran-3-amine (100 mg, 0.62 mmol) were added thereto at 0 C. The mixture was stirred at room temperature for 1 hour, then water (50 mL) and dichloromethane (50 mL) were added thereto. The dichloromethane layer was washed with water (250 mL), brine (50 mL), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated to get a crude product, which was further purified by silica gel column chromatography with dichloromethane/tetrahydrofuran (2/1 by volume) as an eluent to obtain the target compound (colorless oil, 220 mg, yield: 76.17%).

(398) LCMS (ESI) m/z: 420 (M+1)

Example 66E

2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-6,7-dihydro-4H-pyrano[3,4-d]oxazole

(399) ##STR00215##

(400) To a solution of (4.sup.1S,13aS)-N-(4,4-dimethoxy-tetrahydro-2H-pyran-3-yl)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide (120 mg, 0.258 mmol) in acetonitrile (10 mL) was added two drops of N,N-dimethylformamide under an atmosphere of nitrogen, then phosphorus oxychloride (350 mg, 2.28 mmol) was slowly added thereto, and the reaction mixture was heated to 80-90 C. and stirred for 4 hours. The reaction mixture was concentrated and the residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound (40 mg, yield: 35%).

(401) .sup.1H NMR (400 MHz, MeOD-d.sub.4) ppm 7.57-7.64 (m, 1H), 7.13-7.24 (m, 2H), 6.57-6.64 (m, 1H), 5.93 (s, 1H), 5.16 (s, 1H), 4.69 (s, 2H), 3.99-4.17 (m, 2H), 3.79-3.99 (m, 2H), 3.13-3.30 (m, 3H), 2.90 (t, J=5.27 Hz, 2H), 1.89-2.11 (m, 3H), 1.74-1.89 (m, 2H), 1.32 (td, J=14.12, 3.89 Hz, 1H), 1.14 (t, J=7.40 Hz, 3H).

(402) LCMS (ESI) m/z: 402 (M+1)

(403) ##STR00216##

Example 67

4-(2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4-methyloxazol-5-yl)morpholine

(404) ##STR00217##

Example 67A

Tert-butyl-(1-morpholinyl-1-oxopropan-2-yl)-carbamate

(405) ##STR00218##

(406) To a solution of 2-(tert-butoxycarbonylamino)-propionic acid (2.0 g, 10.57 mmol) and morpholine (1.11 g, 12.68 mmol) in dichloromethane (30 mL) was added only one time O-(7-azabenzotriazole-1-yl)-N,N,N,N-tetramethyluronium hexafluoro-phosphate (4.82 g, 12.68 mmol) under an atmosphere of nitrogen, then diisopropylethylamine (3.01 g, 23.25 mmol) was added and the reaction mixture was stirred at room temperature for 15 hour. 20 mL water was added to the mixture, and the aqueous phase was extracted with ethyl acetate (350 mL). The combined organic phase was washed with saturated brine (20 mL), dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under vacuum. The residue was purified by silica gel column chromatography with tetrahydrofuran/petroleum ether (0-1/2 by volume) as an eluent to obtain the target compound (colorless oil, 2.5 g, yield: 91.56%).

(407) .sup.1H NMR (400 MHz, DMSO-d.sub.6) ppm 6.97 (d, J=7.8 Hz, 1H), 4.40 (quin, J=7.2 Hz, 1H), 3.54 (d, J=4.3 Hz, 4H), 3.45 (td, J=4.6, 13.4 Hz, 4H), 1.36 (s, 9H), 1.12 (d, J=6.8 Hz, 3H).

Example 67B

2-amino-1-morpholinyl-propyl-1-one

(408) ##STR00219##

(409) To a solution of tert-butyl-(1-morpholinyl-1-oxopropan-2-yl)-carbamate (900 mg, 3.48 mmol) in dichloromethane (15 mL) was added trifluoroacetic acid (5 mL) under an atmosphere of nitrogen and the mixture was reacted at 15 C. for 2 hours. The mixture was concentrated at 40 C. under reduced pressure. The residue was diluted with 20 mL sodium bicarbonate solution and the aqueous phase was extracted with dichloromethane (330 mL). The combined organic phases were washed with saturated brine (20 mL), dried over anhydrous sodium sulfate, filtered and concentrated under vacuum to obtain the target compound (light yellow liquid, 400 mg, yield: 72.66%).

(410) .sup.1H NMR (400 MHz, DMSO-d.sub.6) ppm 3.75 (q, J=6.6 Hz, 1H), 3.60-3.52 (m, 1H), 3.50-3.40 (m, 4H), 1.07 (d, J=6.8 Hz, 3H).

Example 67C

(41S,13aS)-13a-ethyl-N-(1-morpholinyl-1-oxopropyl-2-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide

(411) ##STR00220##

(412) To a solution of (4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-caboxylic acid (800 mg, 2.48 mmol) and 2-amino-1-morpholinyl-propyl-1-one (400.18 mg, 2.53 mmol) in dichloromethane (20 mL) was added O-(7-azabenzotriazole-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (1.13 g, 2.98 mmol) and triethylamine (552.09 mg, 5.46 mmol) under an atmosphere of nitrogen, respectively, and the reaction mixture was stirred at 20 C. for 15 hour. 20 mL water was added to the mixture, and the aqueous phase was extracted with ethyl acetate (350 mL). The combined organic phase was washed with saturated brine (20 mL), dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under vacuum. The residue was purified by silica gel column chromatography with tetrahydrofuran/petroleum ether (1/5-4/5 by volume) as an eluent to obtain the target compound (yellow solid, 350 mg, yield: 30.51%).

(413) .sup.1H NMR (400 MHz, CHLOROFORM-d) ppm 7.49-7.43 (m, 1H), 7.24-7.18 (m, 1H), 7.15-7.08 (m, 2H), 7.05 (d, J=7.3 Hz, 1H), 5.69 (s, 1H), 5.11 (quin, J=6.9 Hz, 1H), 4.15 (s, 1H), 3.82-3.52 (m, 8H), 3.39-3.31 (m, 1H), 3.30-3.20 (m, 1H), 3.08-2.96 (m, 1H), 2.66-2.60 (m, 2H), 2.51 (dd, J=2.9, 16.2 Hz, 1H), 1.97-1.81 (m, 3H), 1.78-1.63 (m, 1H), 1.55-1.45 (m, 4H), 1.39 (br. s., 1H), 1.07-0.95 (m, 4H).

Example 67D

4-(2-((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1, 5]naphthyridin-12-yl)-4-methyloxazol-5-yl)morpholine

(414) ##STR00221##

(415) A solution of liquid bromine (128.52 mg, 0.804 mmol) in dichloromethane (2 mL) was added dropwise to a solution of triphenylphosphine (210.93 mg, 0.804 mmol) in dichloromethane (10 mL), the mixture was stirred for 30 minutes, triethylamine (203.44 mg, 2.01 mmol) and a solution of (4.sup.1S,13aS)-13a-ethyl-N-(1-morpholinyl-1-oxopropyl-2-yl)-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-carboxamide (310 mg, 0.67 mmol) in dichloromethane (8 mL) were added, respectively, and the reaction mixture was refluxed under an atmosphere of nitrogen for 30 minutes and maintained at 20 C. for more than 12 hours. The mixture was diluted with petroleum ether (50 mL) and the precipitated triethylamine hydrobromide was filtered off. The filtrate was evaporated to dryness under reduced pressure and the residue was purified by basic High Performance Liquid Chromatography to obtain the target compound (100 mg, yield: 33.57%).

(416) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) ppm 7.45 (d, J=7.0 Hz, 1H), 7.11-6.98 (m, 2H), 6.34 (d, J=7.8 Hz, 1H), 5.72 (s, 1H), 4.28 (s, 1H), 3.78-3.70 (m, 4H), 3.37-3.24 (m, 1H), 3.11-2.98 (m, 5H), 2.68-2.53 (m, 3H), 2.21 (s, 3H), 2.04-1.82 (m, 2H), 1.79-1.66 (m, 1H), 1.60 (d, J=13.8 Hz, 1H), 1.50-1.40 (m, 1H), 1.12-0.99 (m, 4H).

(417) LCMS (ESI) m/z: 445 (M+1)

(418) ##STR00222## ##STR00223##

Example 68

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-methyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonamide

(419) ##STR00224##

Example 68A

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-methyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonic acid

(420) ##STR00225##

(421) Chlorosulfonic acid (2.0 g, 17.21 mmol) was added dropwise to a solution of 2-((4.sup.1S,13aS)-13a-ethyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)-4,5-dimethyloxazole (1.5 g, 4.02 mmol) in chloroform (40 mL) at 0-5 C. over a period of 10-15 minutes, and the reaction mixture was stirred at 20 C. for 0.5 hour, and 30 mL chloroform was added thereto. The mixture was poured into ice water, the pH was adjusted to 8 with triethylamine. The mixture was extracted with 50 mL dichloromethane, and the organic phase was washed with water (50 mL), dried over anhydrous sodium sulfate and concentrated. The residue was purified by Preparative High Performance Liquid Chromatography to obtain (4.sup.1S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-methyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-8-sulfonic acid (yellow solid, 600 mg, yield: 32.91%) and (4.sup.1S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-methyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-7-sulfonic acid (210 mg, yield: 11.52%).

(422) .sup.1H NMR (400 MHz, DMSO-d.sub.6) ppm 0.97 (t, J=7.28 Hz, 3H), 1.06-1.14 (m, 1H), 1.57-1.83 (m, 4H), 1.87-1.98 (m, 1H), 2.13 (s, 3H), 2.30 (s, 3H), 2.95-3.11 (m, 3H), 3.21 (d, J=11.29 Hz, 1H), 3.68-3.88 (m, 2H), 5.17 (br. s., 1H), 5.81 (s, 1H), 7.02 (s, 1H), 7.41-7.46 (m, 1H), 7.48-7.51 (m, 1H), 10.49 (br. s., 1H).

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-methyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-8-sulfonic acid

(423) ##STR00226##

(424) .sup.1H NMR (400 MHz, DMSO-d.sub.6) ppm 0.97 (t, J=7.03 Hz, 3H), 1.06-1.21 (m, 1H), 1.54-1.83 (m, 4H), 1.88-1.98 (m, 1H), 2.13 (s, 3H), 2.30 (s, 3H), 3.11 (br. s., 3H), 3.22 (d, J=11.54 Hz, 1H), 3.72-3.86 (m, 2H), 5.17 (br. s., 1H), 5.80 (s, 1H), 6.47 (d, J=8.78 Hz, 1H), 7.39 (d, J=8.78 Hz, 1H), 7.82 (s, 1H), 10.47 (br. s., 1H).

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-methyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-7-sulfonic acid

(425) ##STR00227##

(426) .sup.1H NMR (400 MHz, DMSO-d.sub.6) ppm 0.98 (t, J=7.28 Hz, 3H), 1.11-1.21 (m, 1H), 1.58-1.85 (m, 4H), 1.92 (dq, J=14.37, 7.26 Hz, 1H), 2.13 (s, 3H), 2.28 (s, 3H), 2.93-3.04 (m, 1H), 3.25 (d, J=11.54 Hz, 1H), 3.37-3.50 (m, 1H), 3.69 (br. s., 3H), 5.17 (br. s., 1H), 5.79 (s, 1H), 6.34 (d, J=8.53 Hz, 1H), 7.02 (t, J=7.91 Hz, 1H), 7.48 (d, J=7.28 Hz, 1H), 10.31 (d, J=7.53 Hz, 1H).

Example 68B

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-methyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonylchloride

(427) ##STR00228##

(428) To a solution of (4.sup.1S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-methyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonic acid (300 mg, 0.66 mmol) in chloroform (10 mL) was added thionyl chloride (236 mg, 1.98 mmol) and N,N-dimethylformamide (95 mg, 1.3 mmol), and the reaction mixture was heated to 55 C. and stirred for 2 hours. After the low boiling components were concentrated to dry, the resulting yellow oil was directly used for the next step.

Example 68C

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-methyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonamide

(429) ##STR00229##

(430) To a solution of (4.sup.1S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-methyl-2,3,4.sup.1,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonylchloride (100 mg, 0.212 mmol) in chloroform was respectively added triethylamine (60 mg, 0.632 mmol) and a solution of methylamine in tetrahydrofuran (1 M, 0.426 mL, 0.426 mmol), and the reaction mixture was stirred at 20 C. for 1 hour. Dichloromethane (30 mL) and water (20 mL) was added to the mixture, and the separated organic lay was dried over anhydrous sodium sulfate and concentrated. The residue was purified by Preparative High Performance Liquid Chromatography to obtain the target compound.

(431) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 1.15 (t, J=7.40 Hz, 3H), 1.28-1.38 (m, 1H), 1.77-1.88 (m, 2H), 1.94-2.13 (m, 3H), 2.23 (s, 3H), 2.39 (s, 3H), 2.48 (s, 3H), 3.19-3.30 (m, 2H), 3.38 (br. s., 2H), 3.83-3.99 (m, 2H), 5.22 (br. s., 1H), 6.04 (s, 1H), 7.29 (s, 1H), 7.64 (d, J=8.28 Hz, 1H), 7.80 (d, J=8.28 Hz, 1H).

Example 69

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N,N-dimethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonamide

(432) ##STR00230##

(433) The process of the example was the same as that of Example 68C.

(434) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 1.15 (t, J=7.40 Hz, 3H), 1.34 (td, J=14.18, 4.02 Hz, 1H), 1.77-1.88 (m, 2H), 1.94-2.13 (m, 3H), 2.20 (s, 3H), 2.39 (s, 3H), 2.65 (s, 6H), 3.19-3.31 (m, 2H), 3.33-3.41 (m, 2H), 3.85-4.00 (m, 2H), 5.24 (s, 1H), 6.04 (s, 1H), 7.20 (s, 1H), 7.58 (dd, J=8.28, 1.25 Hz, 1H), 7.83 (d, J=8.28 Hz, 1H).

Example 70

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-(3-methoxylpropyl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonamide

(435) ##STR00231##

(436) The process of the example was the same as that of Example 68C.

(437) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 1.15 (t, J=7.28 Hz, 3H), 1.28-1.37 (m, 1H), 1.65 (quin, J=6.46 Hz, 2H), 1.76-1.87 (m, 2H), 1.96-2.15 (m, 3H), 2.24 (s, 3H), 2.40 (s, 3H), 2.77-2.94 (m, 2H), 3.18-3.32 (m, 6H), 3.34-3.40 (m, 3H), 3.84-3.99 (m, 2H), 5.22 (s, 1H), 6.04 (s, 1H), 7.29 (s, 1H), 7.65 (dd, J=8.28, 1.25 Hz, 1H), 7.79 (d, J=8.53 Hz, 1H).

Example 71

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N,N-dimethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-8-sulfonamide

(438) ##STR00232##

(439) The process of the example was the same as that of Examples 68B, 68C.

(440) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 1.14 (t, J=7.28 Hz, 3H), 1.26-1.38 (m, 1H), 1.76-1.87 (m, 2H), 1.95-2.15 (m, 3H), 2.23 (s, 3H), 2.39 (s, 3H), 2.68 (s, 6H), 3.22-3.30 (m, 2H), 3.33-3.43 (m, 2H), 3.84-4.00 (m, 2H), 5.22 (s, 1H), 6.04 (s, 1H), 6.87 (d, J=8.78 Hz, 1H), 7.57 (dd, J=8.91, 1.38 Hz, 1H), 8.06 (d, J=1.00 Hz, 1H).

Example 72

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-(3-methoxylpropyl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonamide

(441) ##STR00233##

(442) The process of the example was the same as that of Examples 68B, 68C.

(443) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 1.14 (t, J=7.28 Hz, 3H), 1.27-1.37 (m, 1H), 1.70 (quin, J=6.40 Hz, 2H), 1.75-1.87 (m, 2H), 1.94-2.13 (m, 3H), 2.22 (s, 3H), 2.38 (s, 3H), 2.90 (t, J=6.90 Hz, 2H), 3.20-3.32 (m, 6H), 3.39 (t, J=6.02 Hz, 3H), 3.84-4.01 (m, 2H), 5.20 (br. s., 1H), 6.02 (s, 1H), 6.82 (d, J=9.03 Hz, 1H), 7.64 (dd, J=8.78, 1.25 Hz, 1H), 8.14 (s, 1H).

Example 73

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-methyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-7-sulfonamide

(444) ##STR00234##

(445) The process of the example was the same as that of Examples 68B, 68C.

(446) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 1.14 (t, J=7.28 Hz, 3H), 1.31 (td, J=14.05, 3.51 Hz, 1H), 1.75-1.87 (m, 2H), 1.93-2.12 (m, 3H), 2.22 (s, 3H), 2.37 (s, 3H), 2.68-2.74 (m, 3H), 3.20-3.30 (m, 1H), 3.34-3.40 (m, 1H), 3.52-3.69 (m, 2H), 3.80-3.91 (m, 2H), 5.22 (s, 1H), 6.04 (s, 1H), 6.81 (d, J=8.28 Hz, 1H), 7.29 (t, J=8.03 Hz, 1H), 7.68 (d, J=7.53 Hz, 1H).

Example 74

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N,N-dimethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-7-sulfonamide

(447) ##STR00235##

(448) The process of the example was the same as that of Examples 68B, 68C.

(449) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 1.14 (t, J=7.28 Hz, 3H), 1.31 (td, J=13.99, 3.64 Hz, 1H), 1.76-1.86 (m, 2H), 1.95-2.11 (m, 3H), 2.23 (s, 3H), 2.37 (s, 3H), 2.92 (s, 6H), 3.19-3.29 (m, 1H), 3.34-3.40 (m, 1H), 3.49-3.61 (m, 2H), 3.81-3.92 (m, 2H), 5.22 (s, 1H), 6.07 (s, 1H), 6.87 (d, J=8.53 Hz, 1H), 7.31 (t, J=8.16 Hz, 1H), 7.64 (d, J=7.53 Hz, 1H).

Example 75

(41S,13aS)-12-(4,5-dimethyloxazol-2-yl)-13a-ethyl-N-(3-methoxylpropyl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-7-sulfonamide

(450) ##STR00236##

(451) The process of the example was the same as that of Examples 68B, 68C.

(452) .sup.1H NMR (400 MHz, METHANOL-d4) ppm 1.14 (t, J=7.28 Hz, 3H), 1.31 (td, J=13.93, 3.76 Hz, 1H), 1.73-1.87 (m, 4H), 1.93-2.09 (m, 3H), 2.22 (s, 3H), 2.36 (s, 3H), 3.11-3.17 (m, 2H), 3.22-3.31 (m, 4H), 3.36 (br. s., 1H), 3.41 (t, J=6.02 Hz, 2H), 3.54-3.70 (m, 2H), 3.79-3.93 (m, 2H), 5.23 (br. s., 1H), 6.04 (s, 1H), 6.80 (d, J=8.28 Hz, 1H), 7.29 (t, J=8.03 Hz, 1H), 7.70 (d, J=7.53 Hz, 1H).

Example 76

(41S,13aS)-13a-ethyl-N-methyl-12-(3-methyl-1,2,4-oxadiazol-5-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonamide

(453) ##STR00237##

(454) The process of the example was the same as that of Examples 68A, 68B, 68C.

(455) .sup.1H NMR (400 MHz, CD.sub.3OD) O ppm 8.10 (s, 1H), 7.62 (dd, J=1.1, 8.9 Hz, 1H), 7.04 (d, J=9.0 Hz, 1H), 6.41 (s, 1H), 5.23 (br. s., 1H), 4.06-3.78 (m, 2H), 3.32-3.16 (m, 3H), 2.60-2.42 (m, 7H), 2.22-1.93 (m, 3H), 1.87-1.70 (m, 2H), 1.42-1.25 (m, 1H), 1.15 (t, J=7.3 Hz, 3H).

(456) LCMS (ESI) m/z: 444 (M+1)

Example 77

(41S,13aS)-13a-ethyl-N,N-dimethyl-12-(3-methyl-1,2,4-oxadiazol-5-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonamide

(457) ##STR00238##

(458) The process of the example was the same as that of Examples 68A, 68B, 68C.

(459) .sup.1H NMR (400 MHz, CD.sub.3OD) ppm 8.07 (d, J=1.3 Hz, 1H), 7.60 (dd, J=1.5, 9.0 Hz, 1H), 7.11 (d, J=9.0 Hz, 1H), 6.44 (s, 1H), 5.25 (br. s., 1H), 4.07-3.82 (m, 2H), 3.29-3.16 (m, 2H), 2.78-2.65 (m, 7H), 2.54 (s, 3H), 2.21-1.96 (m, 3H), 1.91-1.75 (m, 2H), 1.43-1.30 (m, 3H), 1.16 (t, J=7.3 Hz, 3H).

(460) LCMS (ESI) m/z: 468 (M+1)

Example 78

(41S,13aS)-13a-ethyl-N-(3-methoxylpropyl)-12-(3-methyl-1,2,4-oxadiazol-5-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-9-sulfonamide

(461) ##STR00239##

(462) The process of the example was the same as that of Examples 68A, 68B, 68C.

(463) .sup.1H NMR (400 MHz, CD.sub.3OD) ppm 8.12 (d, J=1.0 Hz, 1H), 7.65 (dd, J=1.5, 8.8 Hz, 1H), 7.05 (d, J=9.0 Hz, 1H), 6.42 (s, 1H), 5.23 (br. s., 1H), 4.04-3.82 (m, 2H), 3.41-3.35 (m, 3H), 3.29-3.19 (m, 5H), 2.90 (t, J=6.9 Hz, 2H), 2.53 (s, 3H), 2.23-1.98 (m, 3H), 1.90-1.77 (m, 2H), 1.69 (quin, J=6.5 Hz, 2H), 1.40-1.26 (m, 2H), 1.15 (t, J=7.3 Hz, 3H).

(464) LCMS (ESI) m/z: 502 (M+1)

Example 79

(41S,13aS)-13a-ethyl-N-methyl-12-(3-methyl-1,2,4-oxadiazol-5-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-8-sulfonamide

(465) ##STR00240##

(466) The process of the example was the same as that of Examples 68A, 68B, 68C.

(467) .sup.1H NMR (400 MHz, CD.sub.3OD) ppm 7.80 (d, J=8.3 Hz, 1H), 7.67 (d, J=8.3 Hz, 1H), 7.51 (s, 1H), 6.45 (s, 1H), 5.25 (s, 1H), 4.08-3.81 (m, 2H), 3.31-3.17 (m, 3H), 2.63-2.44 (m, 7H), 2.20-1.96 (m, 3H), 1.92-1.73 (m, 2H), 1.47-1.28 (m, 2H), 1.16 (t, J=7.3 Hz, 3H).

(468) LCMS (ESI) m/z: 444 (M+1)

Example 80

(41S,13aS)-13a-ethyl-N,N-dimethyl-12-(3-methyl-1,2,4-oxadiazol-5-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-8-sulfonamide

(469) ##STR00241##

(470) The process of the example was the same as that of Examples 68A, 68B, 68C.

(471) .sup.1H NMR (400 MHz, CD.sub.3OD) ppm 7.86 (d, J=8.3 Hz, 1H), 7.63 (d, J=8.3 Hz, 1H), 7.44 (s, 1H), 6.48 (s, 1H), 5.26 (br. s., 1H), 4.01-3.86 (m, 2H), 3.32-3.21 (m, 4H), 2.67 (s, 6H), 2.51 (s, 3H), 2.17-1.92 (m, 3H), 1.91-1.78 (m, 2H), 1.44-1.32 (m, 1H), 1.16 (t, J=7.3 Hz, 3H).

Example 81

(41S,13aS)-13a-ethyl-N-(3-methoxylpropyl)-12-(3-methyl-1,2,4-oxadiazol-5-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-8-sulfonamide

(472) ##STR00242##

(473) The process of the example was the same as that of Examples 68A, 68B, 68C.

(474) .sup.1H NMR (400 MHz, CD.sub.3OD) ppm 7.80 (d, J=8.5 Hz, 1H), 7.69 (dd, J=1.0, 8.5 Hz, 1H), 7.52 (s, 1H), 6.44 (s, 1H), 5.25 (s, 1H), 4.02-3.84 (m, 2H), 3.37 (t, J=6.0 Hz, 3H), 3.32-3.19 (m, 6H), 2.99-2.79 (m, 2H), 2.53 (s, 3H), 2.16-1.94 (m, 3H), 1.90-1.77 (m, 2H), 1.67 (quin, J=6.5 Hz, 2H), 1.42-1.29 (m, 1H), 1.16 (t, J=7.3 Hz, 3H).

(475) LCMS (ESI) m/z: 502 (M+1)

Example 82

(41S,13aS)-13a-ethyl-N-methyl-12-(3-methyl-1,2,4-oxadiazol-5-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-7-sulfonamide

(476) ##STR00243##

(477) The process of the example was the same as that of Examples 68A, 68B, 68C.

(478) .sup.1H NMR (400 MHz, CD.sub.3OD) ppm 7.71 (d, J=7.5 Hz, 1H), 7.32 (t, J=8.2 Hz, 1H), 7.06 (d, J=8.5 Hz, 1H), 6.43 (s, 1H), 5.24 (s, 1H), 3.93-3.79 (m, 2H), 3.71-3.49 (m, 2H), 3.33-3.24 (m, 2H), 2.72 (s, 3H), 2.52 (s, 3H), 2.14-1.94 (m, 3H), 1.90-1.76 (m, 2H), 1.34 (dt, J=3.8, 14.1 Hz, 1H), 1.15 (t, J=7.3 Hz, 3H).

(479) LCMS (ESI) m/z: 444 (M+1)

Example 83

(41S,13aS)-13a-ethyl-N,N-dimethyl-12-(3-methyl-1,2,4-oxadiazol-5-yl)-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-7-sulfonamide

(480) ##STR00244##

(481) The process of the example was the same as that of Examples 68A, 68B, 68C.

(482) .sup.1H NMR (400 MHz, CD.sub.3OD) ppm 7.66 (d, J=7.8 Hz, 1H), 7.34 (t, J=8.2 Hz, 1H), 7.10 (d, J=8.5 Hz, 1H), 6.45 (s, 1H), 5.24 (s, 1H), 3.93-3.80 (m, 2H), 3.64-3.47 (m, 2H), 3.43-3.35 (m, 1H), 3.30-3.19 (m, 2H), 2.93 (s, 6H), 2.72 (s, 1H), 2.52 (s, 3H), 2.16-1.94 (m, 3H), 1.90-1.77 (m, 2H), 1.40-1.28 (m, 3H), 1.15 (t, J=7.3 Hz, 3H).

(483) LCMS (ESI) m/z: 468 (M+1)

Example 84

(41S,13aS)-13a-ethyl-N-(3-methoxylpropyl)-12-(3-methyl-1,2,4-oxadiazol-5-yl)-2,3,4,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-7-sulfonamide

(484) ##STR00245##

(485) The process of the example was the same as that of Examples 68A, 68B, 68C.

(486) .sup.1H NMR (400 MHz, CD.sub.3OD) ppm 7.72 (d, J=7.8 Hz, 1H), 7.32 (t, J=8.2 Hz, 1H), 7.06 (d, J=8.5 Hz, 1H), 6.44 (s, 1H), 5.26 (s, 1H), 3.97-3.81 (m, 2H), 3.72-3.51 (m, 3H), 3.45-3.36 (m, 4H), 3.30-3.24 (m, 4H), 3.16 (t, J=6.8 Hz, 2H), 3.06 (t, J=6.9 Hz, 1H), 2.52 (s, 3H), 2.13-1.74 (m, 8H), 1.41-1.27 (m, 1H), 1.15 (t, J=7.4 Hz, 3H).

(487) LCMS (ESI) m/z: 502 (M+1)

(488) Test 1: In Vitro Detection of Phosphodiesterase (PDE)

(489) Experimental Principle:

(490) the enzyme activity of PDE1A was determined by detecting the production of AMP/GMP by fluorescence polarization immunoassay, wherein AlexaFluor 633 labeled AMP/GMP was used to replace AMP/GMP to bind with the antibody.

(491) Experiment Reagent:

(492) Reaction buffer: 10 mM Tris-HCl, pH 7.5, 5 mM magnesium chloride, 0.01% Brij 35, 1 mM DTT and 1% DMSO;

(493) Enzyme substrate: 1M cAMP or cGMP (Ca.sup.2+-calmodulin acts as a cofactor of PDE1A)

(494) Detection reagent: Transcreener AMP2/GMP2 antibody; AMP2/GMP2 AlexaFluor 633 tracer.

(495) Experimental Procedure and Method:

(496) 1. Human-derived enzyme (commercially available from SignalChem) to be tested and substrate were diluted with freshly prepared reaction buffer;

(497) 2. The enzyme solution (with a concentration of 3 pM) was added to the holes of the microplates;

(498) 3. A series of solutions of the compounds in 100% DMSO (with the desired concentrations) were added to the holes containing the enzyme solution by Echo550, and then the microplates were incubated for 10 minutes at room temperature;

(499) 4. The substrate solution was added to the holes containing the enzyme and compounds to start the reaction;

(500) 5. The microplates were incubated for 1 hour under room temperature and vibration;

(501) 6. The detection mixture (tracer and antibody in stop buffer) was added to stop the enzyme reaction, and the microplates were incubated for 90 minutes under vibration;

(502) 7. The equipment EnVision (PerkinElmer), Cy5 FP Ex FP 620, Em S-pol 688/P-pol 688, FP mirror D658fp/D688 was used to detect the reaction mixture, and Ex/Em 620/688 was used to detect the fluorescence polarization.

(503) Data Analysis:

(504) In the Excel table, the enzyme activity corresponding to the FP signal was found on the AMP/GMP standard curve by reference to the DMSO negative control, and then was converted to product concentration (nM). GraphPad Prism was used to analyze and calculate the IC.sub.50 values.

(505) The experimental result was shown in Table 1.

(506) TABLE-US-00001 TABLE 1 IC.sub.50s for PDE1 Test samples (target compounds) PDE1 Example 1 D Example 2 B Example 3 D Example 4 C Example 5 D Example 6 B Example 7 C Example 8 C Example 9 B Example 10 B Example 11 C Example 12 B Example 13 C Example 14 B Example 15 D Example 16 B Example 17 B Example 18 D Example 19 D Example 20 B Example 21 D Example 22 C Example 23 B Example 24 C Example 25 B Example 26 D Example 27 D Example 28 D Example 29 B Example 30 D Example 31 B Example 32 D Example 33 B Example 34 B Example 35 B Example 36 C Example 37 B Example 38 C Example 39 B Example 40 B Example 41 A Example 42 B Example 43 C Example 44 C Example 45 C Example 46 C Example 47 B Example 48 B Example 49 D Example 50 B Example 51 B Example 52 A Example 53 A Example 54 B Example 55 A Example 56 A Example 57 A Example 58 A Example 59 A Example 60 B Example 61 A Example 62 B Example 63 A Example 64 A Example 65 A Example 66 A Example 67 A Example 68 A Example 69 B Example 70 A Example 71 B Example 72 C Example 73 B Example 74 B Example 75 C Example 76 B Example 77 C Example 78 C Example 79 B Example 80 C Example 81 C Example 82 C Example 83 C Example 84 D Note: A 1 uM; 1 uM < B 20 uM; 20 uM < C 100 uM; D >100 uM
Test 2: Comparison of Pharmacokinetics in Beagle Dogs

(507) In this study, male Beagle dogs were given the compounds of the examples and vinpocetine (as a control compound) by intravenous injection or oral administration, respectively, then the drug concentration in plasma at different time points was determined by the LC/MS/MS method, so as to investigate the pharmacokinetic characteristics of the two test drugs in Beagle dogs.

(508) Eight healthy adult Beagle dogs with a weight of 7.0 to 10.83 kg (purchased from Beijing Marshall Biotechnology Co., Ltd.) were selected. The formulation for intravenous injection group was DMSO: PEG400: water=5:20:75. A solvent was added to the test compound which had been accurately weighed, after vortex oscillation and ultrasound, a clear solution with a final concentration of 1.0 mg/mL was obtained. The solution was filtered with a filter membrane of 0.22 m and stored at room temperature for use. The formulation for oral administration group was PEG 400: Tween 80: H.sub.2O=40:10:50. A solvent was added to the test compound which had been accurately weighed, after vortex oscillation and ultrasound, a clear solution with a final concentration of 1.5 mg/mL was obtained. The formulations for both the intravenous injection and the oral administration were formulated on the day of administration. The intravenous dose was 1.0 mg/kg, and the oral dose was 3.0 mg/kg. The whole blood for each test compound was respectively taken at 0.083 (for intravenous injection only), 0.25, 0.5, 1, 2, 4, 6, 8 and 24 hours after administration. The whole blood was centrifuged (3000 g, 15 min, 4 C.) to obtain the plasma. The drug concentration in each plasma sample was determined by LC/MS/MS method. The data about drug concentration in plasma was processed by WinNonlin Version 6.3 (Pharsight, Mountain View, Calif.) software, using a non-compartmental model, and the pharmacokinetic parameters were calculated by using the linear-logarithmic trapezoidal method.

(509) TABLE-US-00002 TABLE 2 Pharmacokinetic parameters of the target compound of Example 29 and vinpocetine in Beagle dogs Pharmacokinetic parameters in beagel dogs Intravenous Injection (1 mg/kg) Oral Administration (3 mg/kg) area under the Time area under the Plasma Half-life concentration-time Peak to concentration-time clearance period curve (0-inf, concentration Peak curve (0-inf, (mL/min/kg) (h) nM .Math. h) (nM) (h) nM .Math. h) Bioavailability Vinpocetine 80.5 6.03 588 142 0.5 216 12.3 Example 29 11.97 9.42 4040 1299 1.0 4545 37.5

(510) As shown in Table 2, the compound of Example 29 had a plasma clearance about 85% lower than that of vinpocetine, had a half-life 56% longer than that of vinpocetine, and had an oral bioavailability 3.1 times that of vinpocetine. In non-rodent Beagle dogs, the pharmacokinetics parameters of Example 29 were significantly superior to vinpocetine.

(511) Test 3: Inhibition Effect on Pentylenetetrazole-Kindling Model of Epilepsy in Cynomolgus Monkey

(512) In this test, six male cynomolgus monkeys were selected, and each monkey was intragastrically administrated by nasal feeding. Besides pentylenetetrazole which was administrated by subcutaneous injection, the compound of Example 29 and carbamazepine were consecutively administered for 8 days, respectively. The monkeys were respectively given a solvent prior to the first administration, and were injected subcutaneously with pentylenetetrazole immediately after the last administration. The administration interval between two tests was about 10 days. Pentylenetetrazine was administered once to induce epilepsy prior to the first administration of the compound of Example 29. The dosage was calculated according to the latest weight of the animal, and the date of first administration was designated as Day 1.

(513) Surgical procedure: the animals were fed adaptively for at least one week in feeding facilities, and then they were anesthetized during preoperative preparation according to the company standards. The main operation procedures were as follows: cutting the head skin, fully exposing the skull, stripping the periosteum, and cleaning the skull surface with a dry absorbent cotton; drilling 2 holes on the skull of the cynomolgus monkey with cranial drill, implanting a brain electrode, and fixing it with dental cement; then burying two myoelectric electrodes into the neck muscles of the cynomolgus monkey, and burying eye-electric electrodes into the bilateral eye muscles, fixing the implant body in the abdominal muscle layer. Postoperative care was performed according to the company standards.

(514) The raw data was collected by Ponemah of DSI system, and analyzed and revised by Neuronscore.

(515) The data was shown by meanstandard error (MeanSEM), statistical analysis was performed by t-test and ANOVA. P<0.05 indicated a significant difference, P<0.01 indicated a very significant difference, P<0.001 indicated an extremely significant difference.

(516) The characteristics of electroencephalic response and electroencephalic energy for pentylenetetrazole-kindling epilepsy were observed and analyzed, and then a comparison was made between Example 29 and carbamazepine in terms of the latency for the onset of epilepsy seizure, and the times and lasting time of clonic convulsions and tonic convulsions in cynomolgus monkey pentylenetetrazole-kindling model, so as to compare the pharmacodynamic inhibitory effect of Example 29 and carbamazepine on cynomolgus monkey pentylenetetrazole-kindling model.

(517) After the cynomolgus monkeys were injected subcutaneously with 40 mg/kg pentylenetetole on the back and were induced epilepsy-like behaviors, the electroencephalic response, electromyogrphic response and locomotor activity were detected by DSI wireless remote sensing signal recording system. The cynomolgus monkeys injected with pentylenetetrazole showed characteristic epilepsy-like electroencephalic response and electromyogrphic response. The behaviors were divided into paroxysmal activity, clonic convulsion and tonic convulsions according to the status of epilepsy.

(518) The changes of electroencephalic energy within 4-24 Hz were statistically analyzed when cynomolgus monkeys suffered epileptic seizure within 24 hours after injection of pentylenetetrazole. The results showed that the electroencephalic energy within 4-24 Hz was significantly enhanced when pentylenetetrazole-kindling epilepsy occurred.

(519) After injection of pentylenetetrazole, the latency for the onset of epilepsy seizure was calculated, so as to compare the effect of Example 29 and carbamazepine on the the latency for the onset of epilepsy seizure in pentylenetetrazole-kindling model. The results showed that Example 29 and carbamazepine significantly prolonged the latency for the onset of epilepsy seizure. After continuous administration of 8 days, the latency for the onset of epilepsy seizure in pentylenetetrazole-kindling model was 24.863.97 minutes for the Vehicle group, 45.209.11 minutes for the carbamazepine group, 64.1013.21 minutes for Example 29 group, respectively. There was a significant difference (P<0.05) for both the Example 29 group and the carbamazepine group compared with the solvent control group. The carbamazepine group prolonged 20.34 min than the Vehicle group, a relative increase of 81%; Example 29 prolonged 39.24 min than the Vehicle group, a relative increase of 160%; Example 29 prolonged 18.9 min than the camazepine group, a relative increase of 42%.

(520) Thus, both Example 29 and carbamazepine given the same dosage (10 mg/kg) showed a significant effect on prolonging the latency for the onset of epilepsy seizure, and the effect of Example 29 on prolonging the latency for the onset of epilepsy seizure was significantly superior to (about 42%) that of carmazepine.

(521) Furthermore, both Example 29 and carbamazepine significantly reduced the times of clonic convulsion and tonic convulsion within 24 hours after administration of pentylenetetrazol. The times of clonic convulsion and tonic convulsion were 107.5015.60 for the Vehicle group, 39.2014.92 for the carbamazepine group and 25.77.07 for the Example 29 group, respectively. There was a very significant difference (P<0.01) for both Example 29 group and carbamazepine group compared with Vehicle control group. The carbamazepine group reduced by about 68 times on average compared with the Vehicle Group, a relative reduction of 63%; the Example 29 group reduced by about 82 times on average compared with the Vehicle Group, a relative reduction of 76%; the Example 29 reduced by about 14 times compared with the carbamazepine group, a relative reduction of 36%.

(522) Thus, both Example 29 and carbamazepine given the same dosage (10 mg/kg) significantly reduced the times of clonic convulsion and tonic convulsion, and the effect of Example 29 on reducing the times of seizures was significantly superior to (about 36%) that of carmazepine.

(523) Finally, the effect of Example 29 and carbamazepine on the lasting time of clonic convulsions and tonic convulsions were detected. The results showed that both Example 29 and carbamazepine significantly shortened the lasting time of clonic convulsions and tonic convulsions in pentylenetetrazole-kindled cynomolgus monkeys. The lasting time of clonic convulsions and tonic convulsions was 11.683.15 min for the Vehicle group, 4.712.35 min for the carbamazepine group and 2.610.99 min for the Example 29 group, respectively. There was significant difference (P<0.05) for both Example 29 group and carbamazepine group compared with Vehicle control group. The carbamazepine group shortened 6.97 min on average compared with the Vehicle Group, a relative reduction of 60%; the Example 29 shortened 9.07 min on average compared with the Vehicle group, a relative reduction of 78%; the Example 29 shortened about 2.1 min compared with the carbamazepine group, a relative reduction of 45%.

(524) Thus, both Example 29 and carbamazepine given the same dosage (10 mg/kg) significantly shortened the lasting time of clonic convulsions and tonic convulsions, and the effect of Example 29 on shortening the lasting time of clonic convulsions and tonic convulsions was significantly superior to (about 45%) that of carmazepine.

(525) In conclusion, the results showed that all of the six male cynomolgus monkeys injected subcutaneously with pentylenetetrazole showed epileptiform pattern, convulsion and myotonic discharge; and the compound of Example 29 and carbamazepine not only significantly prolonged the latency for the onset of epilepsy seizure in pentylenetetrazole-kindling cynomolgus monkeys, but also significantly reduced the times and lasting time of clonic convulsion and tonic convulsion within 24 hours after administration of pentylenetetrazol. The data indicated that Example 29 was superior to carbamazepine in terms of all the three main outcome measurements of anti-epileptic effects.