HYDROPYRAZINO[1,2-B]ISOQUINOLINE COMPOUNDS FOR THE TREATMENT OF AUTOIMMUNE DISEASE

Abstract

The present invention relates to compounds of formula (I), wherein R.sup.1 to R.sup.3 are as described herein, and their pharmaceutically acceptable salt, enantiomer or diastereomer thereof, and compositions including the compounds and methods of using the compounds.

##STR00001##

Claims

1. A compound of formula (I), ##STR00046## wherein ##STR00047## R.sup.1 is wherein R.sup.4 is C.sub.1-6alkyl, C.sub.1-6alkoxy, haloC.sub.1-6alkyl, halogen, nitro or cyano; R.sup.4a is C.sub.1-6alkyl or C.sub.3-7cycloalkyl; R.sup.5, R.sup.5a and R.sup.5b are independently selected from H and deuterium; R.sup.6 is H or halogen; R.sup.2 is C.sub.1-6alkyl; R.sup.3 is unsubstituted or substituted heterocyclyl, heterocyclylamino, heterocyclylC.sub.1-6alkylamino or substituted C.sub.1-6alkoxy; or a pharmaceutically acceptable salt thereof.

2. A compound according to claim 1, wherein R.sup.1 is ##STR00048## wherein R.sup.4 is cyano, R is H or deuterium.

3. A compound according to claim 2, wherein R.sup.3 is (aminoC.sub.1-6alkylcarbonyl)-2,5-diazabicyclo[2.2.1]heptanyl; (aminoC.sub.1-6alkylcarbonyl)piperazinyl; (C.sub.1-6alkoxypyrrolidinyl)amino; (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; (halopyrrolidinyl)amino; (hydroxypyrrolidinyl)C.sub.1-6 alkylamino; (morpholinyl)C.sub.1-6alkylamino; 1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl; 3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridinyl; amino(C.sub.1-6alkoxy)pyrrolidinyl; amino-1,4-oxazepanyl; aminohalopyrrolidinyl; aminooxopyrrolidinyl or azetidinylC.sub.1-6alkoxy.

4. A compound of formula (Ia), ##STR00049## wherein R.sup.1 is ##STR00050## wherein R.sup.4 is cyano, R.sup.5 is H or deuterium; R.sup.2 is C.sub.1-alkyl; a) R.sup.3a is (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (halopyrrolidinyl)amino; (hydroxypyrrolidinyl)C.sub.1-6alkylamino; (morpholinyl)C.sub.1-6alkylamino or amino-1,4-oxazepanyl; R.sup.3b is H; or b) R.sup.3a is H; R.sup.3b is (aminoC.sub.1-6alkylcarbonyl)-2,5-diazabicyclo[2.2.1]heptanyl; (aminoC.sub.1-6alkylcarbonyl)piperazinyl; (C.sub.1-6alkoxypyrrolidinyl)amino; (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; (halopyrrolidinyl)amino; 1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl; 3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridinyl; amino(C.sub.1-6alkoxy)pyrrolidinyl; aminohalopyrrolidinyl; aminooxopyrrolidinyl or azetidinylC.sub.1-6alkoxy; or a pharmaceutically acceptable salt thereof.

5. A compound of formula (Ib), ##STR00051## wherein R.sup.1 is ##STR00052## wherein R.sup.4 is cyano, R.sup.5 is H or deuterium; R.sup.2 is C.sub.1-6alkyl; a) R.sup.3a is (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (halopyrrolidinyl)amino; (hydroxypyrrolidinyl)C.sub.1-6alkylamino; (morpholinyl)C.sub.1-6alkylamino or amino-1,4-oxazepanyl; R.sup.3b is H; or b) R.sup.3a is H; R.sup.3b is (aminoC.sub.1-6alkylcarbonyl)-2,5-diazabicyclo[2.2.1]heptanyl; (aminoC.sub.1-6 alkylcarbonyl)piperazinyl; (C.sub.1-6alkoxypyrrolidinyl)amino; (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; (halopyrrolidinyl)amino; 1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl; 3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridinyl; amino(C.sub.1-6alkoxy)pyrrolidinyl; aminohalopyrrolidinyl; aminooxopyrrolidinyl or azetidinylC.sub.1-6alkoxy; or a pharmaceutically acceptable salt thereof.

6. A compound according to claim 4 or 5, wherein R.sup.1 is ##STR00053## wherein R.sup.4 is cyano, R.sup.5 is H or deuterium; R.sup.2 is C.sub.1-6alkyl; R.sup.3a is H; R.sup.3b is (aminoC.sub.1-6alkylcarbonyl)-2,5-diazabicyclo[2.2.1]heptanyl; (aminoC.sub.1-6alkylcarbonyl)piperazinyl; (C.sub.1-6alkoxypyrrolidinyl)amino; (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; (halopyrrolidinyl)amino; 1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl; 3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridinyl; amino(C.sub.1-6alkoxy)pyrrolidinyl; aminohalopyrrolidinyl; aminooxopyrrolidinyl or azetidinylC.sub.1-6alkoxy; or a pharmaceutically acceptable salt thereof.

7. A compound according to claim 6, wherein R.sup.2 is methyl.

8. A compound according to claim 6, wherein R.sup.3b is (2-amino-2-methyl-propanoyl)-2,5-diazabicyclo[2.2.1]heptan-2-yl; (2-amino-2-methyl-propanoyl)piperazin-1-yl; (2-methylpyrrolidine-2-carbonyl)piperazin-1-yl; (4-fluoropyrrolidin-3-yl)amino; (4-methoxypyrrolidin-3-yl)amino; (azetidin-2-yl)methoxy; 1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridin-2-yl; 2-(dimethylamino)ethoxy; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazin-6-yl; 3-amino-4-fluoro-pyrrolidin-1-yl; 3-amino-4-methoxy-pyrrolidin-1-yl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl; 3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridin-2-yl or 4-amino-2-oxo-pyrrolidin-1-yl.

9. A compound according to claim 6, wherein R.sup.3b is (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl or azetidinylC.sub.1-6alkoxy.

10. A compound according to claim 9, wherein R.sup.3b is (2-methylpyrrolidine-2-carbonyl)piperazin-1-yl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazin-6-yl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl or (azetidin-2-yl)methoxy.

11. A compound according to claim 4 or 5, wherein R.sup.1 is ##STR00054## wherein R.sup.4 is cyano, R.sup.5 is H or deuterium; R.sup.2 is C.sub.1-6alkyl; R.sup.3a is H; R.sup.3b is (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl or azetidinylC.sub.1-6alkoxy; or a pharmaceutically acceptable salt thereof.

12. A compound according to claim 11, wherein R.sup.1 is ##STR00055## wherein R.sup.4 is cyano, R.sup.5 is H or deuterium; R.sup.2 is methyl; R.sup.3a is H; R.sup.3b is (2-methylpyrrolidine-2-carbonyl)piperazin-1-yl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazin-6-yl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl or (azetidin-2-yl)methoxy; or a pharmaceutically acceptable salt thereof.

13. A compound selected from: 5-[(4R,11aS)-8-(6-amino-1,4-oxazepan-4-yl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-8-[2-[(3S)-3-hydroxypyrrolidin-1-yl]ethylamino]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-4-methyl-8-[[(2R)-morpholin-2-yl]methylamino]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-8-[[(3S,4R)-4-fluoropyrrolidin-3-yl]amino]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-8-[2-(dimethylamino)ethoxy]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-4-methyl-9-[[(3R,4S)-4-fluoropyrrolidin-3-yl]amino]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-9-[[(3R,4S)-4-methoxypyrrolidin-3-yl]amino]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-9-[(3S,4R)-3-amino-4-fluoro-pyrrolidin-1-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-9-[(3R,4S)-3-amino-4-methoxy-pyrrolidin-1-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-9-[(4aS,7aS)-3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazin-6-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-9-[2-(dimethylamino)ethoxy]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-9-[[(2S)-azetidin-2-yl]methoxy]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-4-methyl-9-[[(3R,4S)-4-fluoropyrrolidin-3-yl]amino]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-4-methyl-9-[4-[(2S)-2-methylpyrrolidine-2-carbonyl]piperazin-1-yl]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-9-[(1S,4S)-5-(2-amino-2-methyl-propanoyl)-2,5-diazabicyclo[2.2.1]heptan-2-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-9-(4-amino-2-oxo-pyrrolidin-1-yl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-4-methyl-9-[(8aS)-3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-4-methyl-9-[(8aR)-3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; 5-[(4R,11aS)-4-methyl-9-(3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridin-2-yl)-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; and 5-[(4R,11aS)-4-methyl-9-(1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridin-2-yl)-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; or a pharmaceutically acceptable salt, enantiomer or diastereomer thereof.

14. A process for the preparation of a compound according to any one of claims 1 to 13 comprising the following step: a) the reaction of compound of formula (V), ##STR00056## and R.sup.3—H via Buchwald-Hartwig amination or Suzuki coupling or Stille coupling or Negishi coupling; wherein R.sup.3—H is an amine or an alcohol; wherein X is halogen or leaving group; R.sup.1 to R.sup.3 are defined as in any one of claims 1 to 12.

15. A compound or pharmaceutically acceptable salt, enantiomer or diastereomer according to any one of claims 1 to 13 for use as therapeutically active substance.

16. A pharmaceutical composition comprising a compound in accordance with any one of claims 1 to 13 and a therapeutically inert carrier.

17. The use of a compound according to any one of claims 1 to 13 for the treatment or prophylaxis of systemic lupus erythematosus or lupus nephritis.

18. The use of a compound according to any one of claims 1 to 13 for the preparation of a medicament for the treatment or prophylaxis of systemic lupus erythematosus or lupus nephritis.

19. The use of a compound according to any one of claims 1 to 13 as the TLR7 or TLR8 or TLR9 antagonist.

20. The use of a compound according to any one of claims 1 to 13 as the TLR7 and TLR8 and TLR9 antagonist.

21. The use of a compound according to any one of claims 1 to 13 for the preparation of a medicament for TLR7 and TLR8 and TLR9 antagonist.

22. A compound or pharmaceutically acceptable salt, enantiomer or diastereomer according to any one of claims 1 to 13 for the treatment or prophylaxis of systemic lupus erythematosus or lupus nephritis.

23. A compound or pharmaceutically acceptable salt, enantiomer or diastereomer according to any one of claims 1 to 13 when manufactured according to a process of claim 14.

24. A method for the treatment or prophylaxis of systemic lupus erythematosus or lupus nephritis, which method comprises administering a therapeutically effective amount of a compound as defined in any one of claims 1 to 13.

Description

DETAILED DESCRIPTION OF THE INVENTION

Definitions

[0010] The term “C.sub.1-6alkyl” denotes a saturated, linear or branched chain alkyl group containing 1 to 6, particularly 1 to 4 carbon atoms, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl and the like. Particular “C.sub.1-6alkyl” groups are methyl, ethyl and n-propyl.

[0011] The term “C.sub.3-7cycloalkyl” denotes a saturated carbon ring containing from 3 to 7 carbon atoms, particularly from 3 to 6 carbon atoms, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and the like. Particular “C.sub.3-7cycloalkyl” groups are cyclopropyl, cyclopentyl and cyclohexyl.

[0012] The term “halogen” and “halo” are used interchangeably herein and denote fluoro, chloro, bromo, or iodo.

[0013] The term “C.sub.1-6alkoxy” denotes C.sub.1-6alkyl-O—.

[0014] The term “halopyrrolidinyl” denotes a pyrrolidinyl substituted once, twice or three times by halogen. Examples of halopyrrolidinyl include, but not limited to, difluoropyrrolidinyl and fluoropyrrolidinyl.

[0015] The term “heterocyclyl” or “heterocyclic” denotes a monovalent saturated or partly unsaturated mono or bicyclic ring system of 3 to 12 ring atoms, comprising 1 to 5 ring heteroatoms selected from N, O and S, the remaining ring atoms being carbon. In particular embodiments, heterocyclyl is a monovalent saturated monocyclic ring system of 4 to 7 ring atoms, comprising 1, 2, or 3 ring heteroatoms selected from N, O and S, the remaining ring atoms being carbon. Examples for monocyclic saturated heterocyclyl are aziridinyl, oxiranyl, azetidinyl, oxetanyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothienyl, pyrazolidinyl, imidazolidinyl, oxazolidinyl, isoxazolidinyl, thiazolidinyl, piperidinyl, tetrahydropyranyl, tetrahydrothiopyranyl, piperazinyl, morpholinyl, thiomorpholinyl, 1,1-dioxo-thiomorpholin-4-yl, azepanyl, diazepanyl, homopiperazinyl, oxazepanyl. Examples for bicyclic saturated heterocyclic ring are azabicyclo[3.2.1]octyl, quinuclidinyl, oxaazabicyclo[3.2.1]octanyl, azabicyclo[3.3.1]nonanyl, oxaaza-bicyclo[3.3.1]nonanyl, azabicyclo[3.1.0]hexanyl, oxodiazaspiro[3.4]octanyl, acetyloxodiazaspiro[3.4]octanyl, thiaazabicyclo[3.3.1]nonanyl, oxoazaspiro[2.4]heptanyl, oxoazaspiro[3.4]octanyl, oxoazabicyclo[3.1.0]hexanyl and dioxotetrahydropyrrolo[1,2-a]pyrazinyl. Examples for bicyclic heterocyclyl include, but not limited to, 1,2,3,4-tetrahydroisoquinolinyl; 5,6,7,8-tetrahydro-1,6-naphthyridinyl; 5,6,7,8-tetrahydro-1,7-naphthyridinyl; 5,6,7,8-tetrahydro-2,6-naphthyridinyl; 5,6,7,8-tetrahydro-2,7-naphthyridinyl; isoindolinyl; 1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridin-2-yl; 3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridin-2-yl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl. Examples of heterocyclyl can be further substituted by C.sub.1-6alkyl, C.sub.3-7cycloalkyl, halogen, hydroxy, aminoC.sub.1-6alkylcarbonyl, C.sub.1-6alkylpyrrolidinylcarbonyl oxo or C.sub.1-6alkoxy.

[0016] The term “heterocyclylamino” denotes heterocyclyl-NH—.

[0017] The term “heterocyclylC.sub.1-6alkylamino” denotes heterocyclyl-C.sub.1-6alkyl-NH—.

[0018] The term “pharmaceutically acceptable salts” denotes salts which are not biologically or otherwise undesirable. Pharmaceutically acceptable salts include both acid and base addition salts.

[0019] The term “pharmaceutically acceptable acid addition salt” denotes those pharmaceutically acceptable salts formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, carbonic acid, phosphoric acid, and organic acids selected from aliphatic, cycloaliphatic, aromatic, araliphatic, heterocyclic, carboxylic, and sulfonic classes of organic acids such as formic acid, acetic acid, propionic acid, glycolic acid, gluconic acid, lactic acid, pyruvic acid, oxalic acid, malic acid, maleic acid, maloneic acid, succinic acid, fumaric acid, tartaric acid, citric acid, aspartic acid, ascorbic acid, glutamic acid, anthranilic acid, benzoic acid, cinnamic acid, mandelic acid, embonic acid, phenylacetic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, and salicyclic acid.

[0020] The term “pharmaceutically acceptable base addition salt” denotes those pharmaceutically acceptable salts formed with an organic or inorganic base. Examples of acceptable inorganic bases include sodium, potassium, ammonium, calcium, magnesium, iron, zinc, copper, manganese, and aluminum salts. Salts derived from pharmaceutically acceptable organic nontoxic bases includes salts of primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins, such as isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, ethanolamine, 2-diethylaminoethanol, trimethamine, dicyclohexylamine, lysine, arginine, histidine, caffeine, procaine, hydrabamine, choline, betaine, ethylenediamine, glucosamine, methylglucamine, theobromine, purines, piperizine, piperidine, N-ethylpiperidine, and polyamine resins.

[0021] The term “A pharmaceutically active metabolite” denotes a pharmacologically active product produced through metabolism in the body of a specified compound or salt thereof. After entry into the body, most drugs are substrates for chemical reactions that may change their physical properties and biologic effects. These metabolic conversions, which usually affect the polarity of the compounds of the invention, alter the way in which drugs are distributed in and excreted from the body. However, in some cases, metabolism of a drug is required for therapeutic effect.

[0022] The term “therapeutically effective amount” denotes an amount of a compound or molecule of the present invention that, when administered to a subject, (i) treats or prevents the particular disease, condition or disorder, (ii) attenuates, ameliorates or eliminates one or more symptoms of the particular disease, condition, or disorder, or (iii) prevents or delays the onset of one or more symptoms of the particular disease, condition or disorder described herein. The therapeutically effective amount will vary depending on the compound, the disease state being treated, the severity of the disease treated, the age and relative health of the subject, the route and form of administration, the judgement of the attending medical or veterinary practitioner, and other factors.

[0023] The term “pharmaceutical composition” denotes a mixture or solution comprising a therapeutically effective amount of an active pharmaceutical ingredient together with pharmaceutically acceptable excipients to be administered to a mammal, e.g., a human in need thereof.

Antagonist of TLR7 and/or TLR8 and/or TLR9

[0024] The present invention relates to (i) a compound of formula (I),

##STR00004##

wherein [0025] R.sup.1 is

##STR00005##

wherein R.sup.4 is C.sub.1-6alkyl, C.sub.1-6alkoxy, haloC.sub.1-6alkyl, halogen, nitro or cyano; R.sup.4a is C.sub.1-6alkyl or C.sub.3-7cycloalkyl; R.sup.5, R.sup.5a and R.sup.5b are independently selected from H and deuterium; R.sup.6 is H or halogen; [0026] R.sup.2 is C.sub.1-6alkyl; [0027] R.sup.3 is unsubstituted or substituted heterocyclyl, heterocyclylamino, heterocyclylC.sub.1-6alkylamino or substituted C.sub.1-6alkoxy;

[0028] or a pharmaceutically acceptable salt thereof.

[0029] A further embodiment of present invention is (ii) a compound of formula (I) according to (i), wherein R.sup.1 is

##STR00006##

wherein R.sup.4 is cyano, R.sup.5 is H or deuterium.

[0030] A further embodiment of present invention is (iii) a compound of formula (I) according to (i) or (ii), wherein R.sup.3 is (aminoC.sub.1-6alkylcarbonyl)-2,5-diazabicyclo[2.2.1]heptanyl; (aminoC.sub.1-6 alkylcarbonyl)piperazinyl; (C.sub.1-6alkoxypyrrolidinyl)amino; (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; (halopyrrolidinyl)amino; (hydroxypyrrolidinyl)C.sub.1-6 alkylamino; (morpholinyl)C.sub.1-6alkylamino; 1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl; 3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridinyl; amino(C.sub.1-6alkoxy)pyrrolidinyl; amino-1,4-oxazepanyl; aminohalopyrrolidinyl; aminooxopyrrolidinyl or azetidinylC.sub.1-6alkoxy.

[0031] Another embodiment of present invention is (iv) a compound of formula (Ia),

##STR00007##

[0032] wherein [0033] R.sup.1 is

##STR00008##

wherein R.sup.4 is cyano, R.sup.5 is H or deuterium; [0034] R.sup.2 is C.sub.1-6alkyl; [0035] a) R.sup.3a is (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (halopyrrolidinyl)amino; (hydroxypyrrolidinyl)C.sub.1-6alkylamino; (morpholinyl)C.sub.1-6alkylamino or amino-1,4-oxazepanyl; [0036] R.sup.3b is H; or [0037] b) R.sup.3a is H; [0038] R.sup.3b is (aminoC.sub.1-6alkylcarbonyl)-2,5-diazabicyclo[2.2.1]heptanyl; (aminoC.sub.1-6 alkylcarbonyl)piperazinyl; (C.sub.1-6alkoxypyrrolidinyl)amino; (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; (halopyrrolidinyl)amino; 1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl; 3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridinyl; amino(C.sub.1-6alkoxy)pyrrolidinyl; aminohalopyrrolidinyl; aminooxopyrrolidinyl or azetidinylC.sub.1-6alkoxy;
or a pharmaceutically acceptable salt thereof.

[0039] Another embodiment of present invention is (v) a compound of formula (Ib),

##STR00009##

[0040] wherein [0041] R.sup.1 is

##STR00010##

wherein R.sup.4 is cyano, R.sup.5 is H or deuterium; [0042] R.sup.2 is C.sub.1-6alkyl; [0043] a) R.sup.3a is (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (halopyrrolidinyl)amino; (hydroxypyrrolidinyl)C.sub.1-6alkylamino; (morpholinyl)C.sub.1-6alkylamino or amino-1,4-oxazepanyl; [0044] R.sup.3b is H; or [0045] b) R.sup.3a is H; [0046] R.sup.3b is (aminoC.sub.1-6alkylcarbonyl)-2,5-diazabicyclo[2.2.1]heptanyl; (aminoC.sub.1-6 alkylcarbonyl)piperazinyl; (C.sub.1-6alkoxypyrrolidinyl)amino; (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; (halopyrrolidinyl)amino; 1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl; 3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridinyl; amino(C.sub.1-6alkoxy)pyrrolidinyl; aminohalopyrrolidinyl; aminooxopyrrolidinyl or azetidinylC.sub.1-6alkoxy;
or a pharmaceutically acceptable salt thereof.

[0047] A further embodiment of present invention is (vi) a compound of formula (I) or (Ia) or (Tb) according to any one of (i) to (v), wherein [0048] R.sup.1 is

##STR00011##

wherein R.sup.4 is cyano, R.sup.5 is H or deuterium; [0049] R.sup.2 is C.sub.1-6alkyl; [0050] R.sup.3a is H; [0051] R.sup.3b is (aminoC.sub.1-6alkylcarbonyl)-2,5-diazabicyclo[2.2.1]heptanyl; (aminoC.sub.1-6alkylcarbonyl)piperazinyl; (C.sub.1-6alkoxypyrrolidinyl)amino; (C.sub.1-6alkyl).sub.2aminoC.sub.1-6alkoxy; (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; (halopyrrolidinyl)amino; 1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl; 3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridinyl; amino(C.sub.1-6alkoxy)pyrrolidinyl; aminohalopyrrolidinyl; aminooxopyrrolidinyl or azetidinylC.sub.1-6alkoxy;
or a pharmaceutically acceptable salt thereof.

[0052] A further embodiment of present invention is (vii) a compound of formula (I) or (Ia) or (Ib) according to any one of (i) to (vi), or a pharmaceutically acceptable salt thereof, wherein R.sup.2 is methyl.

[0053] A further embodiment of present invention is (viii) a compound formula (I) or (Ta) or (Tb) according to any one of (i) to (vii), or a pharmaceutically acceptable salt thereof, wherein R.sup.3b is (2-amino-2-methyl-propanoyl)-2,5-diazabicyclo[2.2.1]heptan-2-yl; (2-amino-2-methyl-propanoyl)piperazin-1-yl; (2-methylpyrrolidine-2-carbonyl)piperazin-1-yl; (4-fluoropyrrolidin-3-yl)amino; (4-methoxypyrrolidin-3-yl)amino; (azetidin-2-yl)methoxy; 1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridin-2-yl; 2-(dimethylamino)ethoxy; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazin-6-yl; 3-amino-4-fluoro-pyrrolidin-1-yl; 3-amino-4-methoxy-pyrrolidin-1-yl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl; 3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridin-2-yl or 4-amino-2-oxo-pyrrolidin-1-yl.

[0054] A further embodiment of present invention is (ix) a compound of formula (I) or (Ta) or (Tb) according to any one of (i) to (viii), or a pharmaceutically acceptable salt thereof, wherein R.sup.3b is (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl or azetidinylC.sub.1-6alkoxy.

[0055] A further embodiment of present invention is (x) a compound of formula (I) or (Ta) or (Tb) according to any one of (i) to (ix), wherein R.sup.3b is (2-methylpyrrolidine-2-carbonyl)piperazin-1-yl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazin-6-yl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl or (azetidin-2-yl)methoxy.

[0056] A further embodiment of present invention is (xi) a compound of formula (I) or (Ia) or (Ib) according to any one of (i) to (x), wherein [0057] R.sup.1 is

##STR00012##

wherein R.sup.4 is cyano, R.sup.5 is H or deuterium; [0058] R.sup.2 is C.sub.1-6alkyl; [0059] R.sup.3a is H; [0060] R.sup.3b is (C.sub.1-6alkylpyrrolidinylcarbonyl)piperazinyl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazinyl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazinyl or azetidinylC.sub.1-6alkoxy;
or a pharmaceutically acceptable salt thereof.

[0061] A further embodiment of present invention is (xii) a compound of formula (I) or (Ta) or (Tb) according to any one of (i) to (xi), wherein [0062] R.sup.1 is

##STR00013##

wherein R.sup.4 is cyano, R.sup.5 is H or deuterium; [0063] R.sup.2 is methyl; [0064] R.sup.3a is H; [0065] R.sup.3b is (2-methylpyrrolidine-2-carbonyl)piperazin-1-yl; 3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazin-6-yl; 3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl or (azetidin-2-yl)methoxy;
or a pharmaceutically acceptable salt thereof.

[0066] Another embodiment of present invention is that (xiii) compounds of formula (I) or (Ta) or (Tb) are selected from the following: [0067] 5-[(4R,11aS)-8-(6-amino-1,4-oxazepan-4-yl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0068] 5-[(4R,11aS)-8-[2-[(3S)-3-hydroxypyrrolidin-1-yl]ethylamino]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0069] 5-[(4R,11aS)-4-methyl-8-[[(2R)-morpholin-2-yl]methylamino]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0070] 5-[(4R,11aS)-8-[[(3S,4R)-4-fluoropyrrolidin-3-yl]amino]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0071] 5-[(4R,11aS)-8-[2-(dimethylamino)ethoxy]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0072] 5-[(4R,11aS)-4-methyl-9-[[(3R,4S)-4-fluoropyrrolidin-3-yl]amino]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0073] 5-[(4R,11aS)-9-[[(3R,4S)-4-methoxypyrrolidin-3-yl]amino]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0074] 5-[(4R,11aS)-9-[(3S,4R)-3-amino-4-fluoro-pyrrolidin-1-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0075] 5-[(4R,11aS)-9-[(3R,4S)-3-amino-4-methoxy-pyrrolidin-1-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0076] 5-[(4R,11aS)-9-[(4aS,7aS)-3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazin-6-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0077] 5-[(4R,11aS)-9-[2-(dimethylamino)ethoxy]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0078] 5-[(4R,11aS)-9-[[(2S)-azetidin-2-yl]methoxy]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0079] 5-[(4R,11aS)-4-methyl-9-[[(3R,4S)-4-fluoropyrrolidin-3-yl]amino]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0080] 5-[(4R,11aS)-4-methyl-9-[4-[(2S)-2-methylpyrrolidine-2-carbonyl]piperazin-1-yl]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0081] 5-[(4R,11aS)-9-[(1S,4S)-5-(2-amino-2-methyl-propanoyl)-2,5-diazabicyclo[2.2.1]heptan-2-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0082] 5-[(4R,11aS)-9-(4-amino-2-oxo-pyrrolidin-1-yl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0083] 5-[(4R,11aS)-4-methyl-9-[(8aS)-3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0084] 5-[(4R,11aS)-4-methyl-9-[(8aR)-3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; [0085] 5-[(4R,11aS)-4-methyl-9-(3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridin-2-yl)-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile; and [0086] 5-[(4R,11aS)-4-methyl-9-(1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridin-2-yl)-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile;

[0087] or a pharmaceutically acceptable salt, enantiomer or diastereomer thereof.

Synthesis

[0088] The compounds of the present invention can be prepared by any conventional means. Suitable processes for synthesizing these compounds as well as their starting materials are provided in the schemes below and in the examples. All substituents, in particular, R.sup.1 to R.sup.6 are as defined above unless otherwise indicated. Furthermore, and unless explicitly otherwise stated, all reactions, reaction conditions, abbreviations and symbols have the meanings well known to a person of ordinary skill in organic chemistry.

[0089] A general synthetic route for preparing the compound of formula (I) is shown in Scheme 1 below.

##STR00014##

[0090] wherein X and Y are halogen or leaving group, for example, OTf or OMs; R.sup.7 is protecting group, for example, Boc or benzyl.

[0091] After R.sup.7 is removed from compound of formula (II) by selective deprotection, the resulting compound of formula (III) can react with compound of formula (IV) to afford compound of formula (V) by nucleophilic aromatic substitution in the presence of a base, such as DIEPA, or Buchwald-Hartwig amination conditions (e.g. heating with halide (IV) in the presence of a catalyst, such as Ruphos Pd-G2, and a base, such as Cs.sub.2CO.sub.3. Compound of formula (I) or (Ia) or (Ib) can be obtained from the reaction of compound of formula (V) and R.sup.3—H (R.sup.3—H can be an amine or an alcohol) via metal catalyzed coupling conditions: Buchwald-Hartwig amination in the presence of a catalyst, such as Ruphos Pd-G2, and a base, such as Cs.sub.2CO.sub.3; Suzuki coupling with R.sup.3-boronic acid, R.sup.3-boronic ester, in the presence of a palladium catalyst, such as tetrakis(triphenylphosphine)palladium(0) or [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II), complex with dichloromethane and a base, such as potassium carbonate in solvent; Stille coupling with organotin reagent, in the presence of a palladium(0) catalyst, such as tetrakis(triphenylphosphine)palladium(0); or Negishi coupling with organozinc reagent in the presence of a palladium(0) catalyst, such as tetrakis(triphenylphosphine)palladium(0) or [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II). In some embodiment, a protecting group, e.g. Boc, will be removed and may be further modified by amide formation reactions before affording the final compound of formula (I) or (Ta) or (Tb).

[0092] Compounds of this invention can be obtained as mixtures of diastereomers or enantiomers, which can be separated by methods well known in the art, e.g. (chiral) HPLC or SFC. In another embodiment, compound of formula (Ia) or (Tb) can be obtained according to above scheme by using corresponding chiral starting materials.

[0093] Compounds of this invention can be obtained as mixtures of diastereomers or enantiomers, which can be separated by methods well known in the art, e.g. (chiral) HPLC or SFC.

[0094] This invention also relates to a process for the preparation of a compound of formula (I), (Ia) comprising the following step:

[0095] a) the reaction of compound of formula (V),

##STR00015## [0096] and R.sup.3—H via Buchwald-Hartwig amination or Suzuki coupling or Stille coupling or Negishi coupling; wherein R.sup.3—H is an amine or an alcohol;

[0097] A compound of formula (I) or (Ia) or (Ib) when manufactured according to the above process with achiral or chiral starting materials is also an object of the invention.

Indications and Methods of Treatment

[0098] The present invention provides compounds that can be used as TLR7 and/or TLR8 and/or TLR9 antagonist, which inhibits pathway activation through TLR7 and/or TLR8 and/or TLR9 as well as respective downstream biological events including, but not limited to, innate and adaptive immune responses mediated through the production of all types of cytokines and all forms of auto-antibodies. Accordingly, the compounds of the invention are useful for blocking TLR7 and/or TLR8 and/or TLR9 in all types of cells that express such receptor(s) including, but not limited to, plasmacytoid dendritic cell, B cell, T cell, macrophage, monocyte, neutrophil, keratinocyte, epithelial cell. As such, the compounds can be used as a therapeutic or prophylactic agent for systemic lupus erythematosus and lupus nephritis.

[0099] The present invention provides methods for treatment or prophylaxis of systemic lupus erythematosus and lupus nephritis in a patient in need thereof.

[0100] Another embodiment includes a method of treating or preventing systemic lupus erythematosus and lupus nephritis in a mammal in need of such treatment, wherein the method comprises administering to said mammal a therapeutically effective amount of a compound of formula (I), a stereoisomer, tautomer, prodrug or pharmaceutically acceptable salt thereof.

EXAMPLES

[0101] The invention will be more fully understood by reference to the following examples. They should not, however, be construed as limiting the scope of the invention.

Abbreviations

[0102] The invention will be more fully understood by reference to the following examples. They should not, however, be construed as limiting the scope of the invention.

[0103] Abbreviations used herein are as follows: [0104] ACN: acetonitrile [0105] DCM: dichloromethane [0106] EA or EtOAc: ethyl acetate [0107] FA: formic acid [0108] HATU 1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate [0109] hr hour [0110] hrs hours [0111] IC.sub.50: half inhibition concentration [0112] LCMS liquid chromatography-mass spectrometry [0113] MS: mass spectrometry [0114] PE: petroleum ether [0115] prep-HPLC: preparative high performance liquid chromatography [0116] rt: rt [0117] RuPhos Pd G2: chloro(2-dicyclohexylphosphino-2′,6′-diisopropoxy-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II) 2nd generation [0118] SFC: supercritical fluid chromatography [0119] TFA: trifluoroacetic acid [0120] v/v volume ratio

[0121] General Experimental Conditions

[0122] Intermediates and final compounds were purified by flash chromatography using one of the following instruments: i) Biotage SP1 system and the Quad 12/25 Cartridge module. ii) ISCO combi-flash chromatography instrument. Silica gel brand and pore size: i) KP-SIL 60 Å, particle size: 40-60 μm; ii) CAS registry NO: Silica Gel: 63231-67-4, particle size: 47-60 micron silica gel; iii) ZCX from Qingdao Haiyang Chemical Co., Ltd, pore: 200-300 or 300-400.

[0123] Intermediates and final compounds were purified by preparative HPLC on reversed phase column using XBridge™ Prep-C18 (5 μm, OBD™ 30×100 mm) column, SunFire™ Prep-C18 (5 μm, OBD™ 30×100 mm) column, Phenomenex Synergi-C18 (10 μm, 25×150 mm) or Phenomenex Gemini-C18 (10 μm, 25×150 mm). Waters AutoP purification System (Sample Manager 2767, Pump 2525, Detector: Micromass ZQ and UV 2487, solvent system: acetonitrile and 0.1% ammonium hydroxide in water; acetonitrile and 0.1% FA in water or acetonitrile and 0.1% TFA in water). Or Gilson-281 purification System (Pump 322, Detector: UV 156, solvent system: acetonitrile and 0.05% ammonium hydroxide in water; acetonitrile and 0.225% FA in water; acetonitrile and 0.05% HCl in water; acetonitrile and 0.075% TFA in water; or acetonitrile and water).

[0124] For SFC chiral separation, intermediates were separated by chiral column (Daicel chiralpak IC, 5 μm, 30×250 mm), AS (10 μm, 30×250 mm) or AD (10 μm, 30×250 mm) using Mettler Toledo Multigram III system SFC, Waters 80Q preparative SFC or Thar 80 preparative SFC, solvent system: CO.sub.2 and IPA (0.5% TEA in IPA) or CO.sub.2 and MeOH (0.1% NH.sub.3—H.sub.2O in MeOH), back pressure 100 bar, detection UV@ 254 or 220 nm.

[0125] LC/MS spectra of compounds were obtained using a LC/MS (Waters™ Alliance 2795-Micromass ZQ, Shimadzu Alliance 2020-Micromass ZQ or Agilent Alliance 6110-Micromass ZQ), LC/MS conditions were as follows (running time 3 or 1.5 mins):

[0126] Acidic condition I: A: 0.1% TFA in H.sub.2O; B: 0.1% TFA in acetonitrile;

[0127] Acidic condition II: A: 0.0375% TFA in H.sub.2O; B: 0.01875% TFA in acetonitrile;

[0128] Basic condition I: A: 0.1% NH.sub.3—H.sub.2O in H.sub.2O; B: acetonitrile;

[0129] Basic condition II: A: 0.025% NH.sub.3—H.sub.2O in H.sub.2O; B: acetonitrile;

[0130] Neutral condition: A: H.sub.2O; B: acetonitrile.

[0131] Mass spectra (MS): generally only ions which indicate the parent mass are reported, and unless otherwise stated the mass ion quoted is the positive mass ion (MH).sup.+.

[0132] NMR Spectra were obtained using Bruker Avance 400 MHz.

[0133] The microwave assisted reactions were carried out in a Biotage Initiator Sixty microwave synthesizer. All reactions involving air-sensitive reagents were performed under an argon or nitrogen atmosphere. Reagents were used as received from commercial suppliers without further purification unless otherwise noted.

Preparative Examples

[0134] The following examples are intended to illustrate the meaning of the present invention but should by no means represent a limitation within the meaning of the present invention:

Intermediate A

5-Fluoroquinoline-8-carbonitrile

[0135] ##STR00016##

[0136] The titled compound was synthesized according to the following scheme:

##STR00017##

Step (a): Preparation of 8-bromo-5-fluoro-quinoline (Compound A2)

[0137] In a 100 mL pear-shaped flask, 2-bromo-5-fluoroaniline (compound A1, 2.0 g, 10.5 mmol), propane-1,2,3-triol (969 mg, 10.5 mmol) and sodium 3-nitrobenzenesulfonate (2.4 g, 10.5 mmol) were combined with 70% H.sub.2SO.sub.4 (20 mL) to afford a dark brown solution, which was heated to 150° C. and stirred for 3 hrs. After being cooled to room temperature, the reaction mixture was poured into ice-water, and neutralized with sodium hydroxide solution. The resultant mixture was filtered. The filter cake was dissolved in EtOAc and filtered. The resultant filtrate was concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 40 g, 0% to 30% EtOAc in PE) to afford compound A2 (2.0 g, 84% yield). MS: calc'd 226 and 228 [(M+H).sup.+], measured 226 and 228 [(M+H).sup.+].

Step (b): Preparation of 5-fluoroquinoline-8-carbonitrile (Intermediate A)

[0138] To a solution of 8-bromo-5-fluoroquinoline (compound A2, 4.9 g, 21.7 mmol) in DMF (30 mL) was added dicyanozinc (5.0 g, 43.4 mmol) and RuPhos Pd G2 (CAS: 1375325-68-0, Sigma-Aldrich, Catalog: 753246, 842 mg, 1.1 mmol). The reaction mixture was stirred at 100° C. for 3 hrs, then cooled to room temperature. The reaction mixture was filtered and the filtrate was diluted with water (50 ml), then extracted with EA (80 mL) for three times. The combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica gel, 40 g, 0% to 70% EtOAc in PE) to afford Intermediate A1 (3.0 g, 80% yield). MS: calc'd 173 [(M+H).sup.+], measured 173 [(M+H).sup.+]. .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ ppm 9.11 (dd, J=4.28, 1.71 Hz, 1H), 8.64 (dd, J=8.56, 1.71 Hz, 1H), 8.29 (dd, J=8.19, 5.62 Hz, 1H), 7.76 (dd, J=8.56, 4.28 Hz, 1H), 7.49 (dd, J=9.35, 8.25 Hz, 1H).

Intermediate B

5-[(4R,11aS)-8-bromo-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0139] ##STR00018##

[0140] The titled compound was synthesized according to the following scheme:

##STR00019## ##STR00020##

Step (a): Preparation of Methyl (2S)-3-(4-bromophenyl)-2-(methoxycarbonylamino) propanoate (Compound B2)

[0141] To a solution of methyl (S)-2-amino-3-(4-bromophenyl)propanoate hydrochloride (CAS: 880347-43-3, Bidepharm, Catalog: BD00815750) (compound B1, 9 g, 30.6 mmol) in DCM (100 mL) was added pyridine (6.0 g, 6.2 mL, 76.4 mmol) and methyl carbonochloridate (5.8 g, 61.1 mmol). The reaction mixture was stirred at room temperature overnight, then the mixture was concentrated under reduced pressure. The residue was dissolved in EtOAc, washed with NaHCO.sub.3 aqueous solution, 1N HCl aqueous solution and brine respectively. The organic layer was dried over MgSO.sub.4, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatograph on a silica gel column using 25% Ethyl acetate in hexane to afford the compound B2 (8.5 g, 88% yield). MS: calc'd 316 [(M+H).sup.+], measured 316 [(M+H).sup.+].

Step (b): Preparation of Dimethyl (3S)-7-bromo-3,4-dihydro-1H-isoquinoline-2,3-dicarboxylate (Compound B3)

[0142] To a mixture of methyl (S)-3-(4-bromophenyl)-2-((methoxycarbonyl)amino)propanoate (compound B2, 8.5 g, 26.9 mmol) and paraformaldehyde (1.61 g, 53.8 mmol) was added a mixture of concentrated sulfuric acid (20 mL) and acetic acid (30 mL). The resultant mixture was stirred at room temperature for 20 hrs. The reaction mixture was poured into ice-water, and extracted with DCM. The organic layer was washed with water, saturated NaHCO.sub.3 aqueous solution and brine respectively, dried with MgSO.sub.4. After filtration, the filtrate was concentrated and the residue was purified by flash chromatography (silica gel, 120 g, 0% to 70% EtOAc in hexanes) to afford compound B3 (5.9 g, 66.9% yield). MS: calc'd 328 [(M+H).sup.+], measured 328[(M+H).sup.+].

Step (c): Preparation of Methyl (3S)-7-bromo-1,2,3,4-tetrahydroisoquinoline-3-carboxylate (Compound B4)

[0143] To a solution of dimethyl (S)-7-bromo-3,4-dihydroisoquinoline-2,3(1H)-dicarboxylate (compound B3, 5.9 g, 18.0 mmol) in DCM (40 mL) was added iodotrimethylsilane (14.4 g, 71.9 mmol). The resultant mixture was stirred at 50° C. for 2 hrs. After being cooled to room temperature, methanol (40 mL) was added, then the reaction mixture was stirred for additional 30 min. The reaction mixture was concentrated in vacuo, the residue was diluted with diethyl ether and filtered. The collected solid was washed with ether, dried under vacuum to afford compound B4 (4.6 g, 94.7% yield) which was directly used in the next step without further purification. MS: calc'd 270 [(M+H).sup.+], measured 270 [(M+H).sup.+].

Step (d): Preparation of Methyl (3S)-7-bromo-2-[2-(tert-butoxycarbonylamino)-1-methyl-ethyl]-3,4-dihydro-1H-isoquinoline-3-carboxylate (Compound B5)

[0144] To a solution of methyl (S)-7-bromo-1,2,3,4-tetrahydroisoquinoline-3-carboxylate (compound B4, 4.6 g, 17 mmol) and tert-butyl (2-oxopropyl)carbamate (4.42 g, 25.5 mmol) in methanol (40 mL) was added 0.5 mL HOAc. After the resultant mixture was stirred at reflux for 2 hrs, NaBH.sub.3CN (2.1 g, 34.1 mmol) was added. Then the reaction mixture was stirred at reflux overnight. After the mixture being cooled to room temperature, diluted with water (100 mL), extracted with EA (100 mL) for three times. The combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated. The residue was purified by flash chromatography (silica gel, 80 g, 0% to 70% EtOAc in PE) to afford compound B5 (3.28 g, 45.1% yield). MS: calc'd 427 [(M+H).sup.+], measured 427[(M+H).sup.+].

Step (e): Preparation of (11aS)-8-bromo-4-methyl-2,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-1-one (Compound B6)

[0145] The mixture of methyl (3S)-7-bromo-2-[2-(tert-butoxycarbonylamino)-1-methyl-ethyl]-3,4-dihydro-1H-isoquinoline-3-carboxylate (compound B5, 2.2 g, 5.2 mmol) and HCl/MeOH (10% W/W; 50 mL) was stirred at 60° C. overnight. After being cooled to room temperature, the reaction mixture was basified with sat. K.sub.2CO.sub.3 (aq) to pH about 8, and extracted with EA (80 mL) for three times. The combined organic layer was washed with brine (50 mL), dried over Na.sub.2SO.sub.4 and concentrated in vacuo. The residue was purified by flash chromatography (silica gel, 40 g, 0% to 20% MeOH in DCM) to afford compound B6 (780 mg, 51.3% yield). MS: calc'd 295 [(M+H).sup.+], measured 295 [(M+H).sup.+].

Step (f): Preparation of (11aS)-8-bromo-4-methyl-2,3,4,6,11,11a-hexahydro-1H-pyrazino[1,2-b]isoquinoline (Compound B7)

[0146] A mixture of (11aS)-8-bromo-4-methyl-2,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-1-one (compound B6, 760 mg, 2.57 mmol) and BH.sub.3 solution (1M in THF, 30 mL, 30 mmol) was heated at 80° C. with stirring on for 5 hrs. HCl solution (6 N, 5 mL) was added slowly to the reaction mixture at 0° C. After being stirred at 80° C. for 2 hrs, the mixture was cooled to room temperature, basified with 2 N NaOH solution (aq) to pH 10, and extracted with EtOAc twice. The combined organic layer was dried over MgSO.sub.4, filtered and concentrated in vacuo to afford compound B7 (710 mg, 98.1% yield). MS: calc'd 281 [(M+H).sup.+], measured 281 [(M+H).sup.+].

Step (g): Preparation of 5-[(4R,11aS)-8-bromo-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile (Intermediate B)

[0147] To a solution of (11aS)-8-bromo-4-methyl-2,3,4,6,11,11a-hexahydro-1H-pyrazino[1,2-b]isoquinoline (compound B7, 710 mg, 2.5 mmol) in DMSO (10 mL) was added 5-fluoroquinoline-8-carbonitrile (Intermediate A, 435 mg, 2.5 mmol) and DIEA (1.63 g, 2.2 mL, 12.6 mmol). The resultant mixture was stirred at 120° C. for 20 hrs. After being cooled to room temperature, the reaction was diluted with water (50 mL) and extracted with EA (80 mL) twice. The combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica gel, 40 g, 0% to 100% EtOAc in PE) to afford Intermediate B (510 mg, 46.6% yield) and compound B8 (230 mg, 21% yield). The stereochemistry was confirmed by NOESY.

[0148] Intermediate B MS: calc'd 433 [(M+H).sup.+], measured 433 [(M+H).sup.+]. .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ ppm 9.00 (dd, J=4.22, 1.65 Hz, 1H), 8.64 (dd, J=8.56, 1.59 Hz, 1H), 8.15 (d, J=8.07 Hz, 1H), 7.65 (dd, J=8.56, 4.28 Hz, 1H), 7.35 (s, 1H), 7.31 (dd, J=8.13, 1.90 Hz, 1H), 7.25 (d, J=7.95 Hz, 1H), 7.05 (d, J=8.19 Hz, 1H), 4.37 (d, J=15.65 Hz, 1H), 3.60 (dt, J=11.83, 2.83 Hz, 1H), 3.46 (br d, J=2.57 Hz, 1H), 3.45-3.37 (m, 1H), 3.02-2.94 (m, 1H), 2.91-2.83 (m, 1H), 2.88-2.82 (m, 1H), 2.87-2.80 (m, 1H), 2.74-2.63 (m, 1H), 1.37-1.29 (m, 3H).

[0149] compound B8 MS: calc'd 433 [(M+H).sup.+], measured 433 [(M+H).sup.+]. .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ ppm 8.99 (dd, J=4.22, 1.65 Hz, 1H), 8.69 (dd, J=8.56, 1.59 Hz, 1H), 8.17 (d, J=8.07 Hz, 1H), 7.66 (dd, J=8.56, 4.28 Hz, 1H), 7.39-7.22 (m, 3H), 7.10 (d, J=8.19 Hz, 1H), 4.08-3.98 (m, 2H), 3.62-3.47 (m, 2H), 3.39 (dd, J=11.80, 2.02 Hz, 1H), 3.36-3.43 (m, 1H), 3.28-3.17 (m, 1H), 3.16-3.09 (m, 1H), 3.08-2.97 (m, 1H), 2.82 (dd, J=17.06, 4.95 Hz, 1H), 1.34-1.28 (m, 3H).

Intermediate C

5-[(4R,11aS)-9-bromo-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0150] ##STR00021##

[0151] The title compound was prepared in analogy to the preparation of Intermediate B by using methyl (S)-2-amino-3-(3-bromophenyl)propanoate hydrochloride (CAS: 875782-96-0, Bidepharm, Catalog: BD00869561) instead of methyl (S)-2-amino-3-(4-bromophenyl)propanoate hydrochloride in step (a). Intermediate C was obtained. MS: calc'd 433 [(M+H).sup.+], measured 433 [(M+H).sup.+]. .sup.1H NMR (CHLOROFORM-d, 400 MHz) δ 9.08 (dd, 1H, J=1.6, 4.2 Hz), 8.49 (dd, 1H, J=1.7, 8.6 Hz), 8.05 (d, 1H, J=7.9 Hz), 7.52 (dd, 1H, J=4.2, 8.6 Hz), 7.29 (d, 1H, J=8.2 Hz), 7.26 (br s, 1H), 7.11 (d, 1H, J=8.1 Hz), 6.98 (d, 1H, J=8.2 Hz), 4.30 (d, 1H, J=15.2 Hz), 3.5-3.6 (m, 1H), 3.3-3.4 (m, 2H), 2.7-3.0 (m, 5H), 1.29 (d, 3H, J=6.1 Hz). The stereochemistry was confirmed by NOESY.

Example 1

5-[(4R,11aS)-8-(6-amino-1,4-oxazepan-4-yl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0152] ##STR00022##

[0153] The titled compound was synthesized according to the following scheme:

##STR00023##

Step (a): Preparation of Tert-Butyl N-[4-[(4R,11aS)-2-(8-cyano-5-quinolyl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-8-yl]-1,4-oxazepan-6-yl]carbamate (Compound 1.1)

[0154] To a solution of tert-butyl N-(1,4-oxazepan-6-yl)carbamate (CAS: 1782916-90-8, PharmaBlock, Catalog: PB95734, 60 mg, 277 μmol) in dioxane (5 mL) was added 5-((4R,11aS)-8-bromo-4-methyl-1,3,4,6,11,11a-hexahydro-2H-pyrazino[1,2-b]isoquinolin-2-yl)quinoline-8-carbonitrile (Intermediate B1, 120 mg, 277 μmol), tBuONa (53.3 mg, 555 μmol) and tBuXPhos Pd G3 (CAS: 1447963-75-8, Sigma-Aldrich, Catalog: 762229, 22 mg, 27.7 μmol). The resultant mixture was stirred at 90° C. overnight. After being cooled to room temperature, diluted with water (20 mL), and extracted with EA (20 mL) for three times. The combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica gel, 24 g, 0% to 100% EtOAc in PE) to afford compound 1.1 (33 mg, 20.9% yield). MS: calc'd 569 [(M+H).sup.+], measured 569 [(M+H).sup.+].

Step (b): Preparation of 5-[(4R,11aS)-8-(6-amino-1,4-oxazepan-4-yl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile (Example 1)

[0155] To a solution of tert-butyl N-[4-[(4R,11aS)-2-(8-cyano-5-quinolyl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-8-yl]-1,4-oxazepan-6-yl]carbamate (compound 1.1, 21 mg, 38 μmol) in DCM (2 mL) was added TFA (1 mL). The reaction mixture was stirred at room temperature for 30 min, then concentrated to afford a crude product, which was purified by prep-HPLC to afford Example 1 (9 mg, 50.6% yield). MS: calc'd 469 [(M+H).sup.+], measured 469 [(M+H).sup.+]. .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ ppm 9.09-8.96 (m, 1H), 8.76-8.60 (m, 1H), 8.20 (d, J=7.9 Hz, 1H), 7.74-7.64 (m, 1H), 7.35 (d, J=7.9 Hz, 1H), 7.10 (d, J=8.6 Hz, 1H), 6.88-6.80 (m, 1H), 6.74 (s, 1H), 4.67 (d, J=15.3 Hz, 1H), 4.18-4.10 (m, 1H), 4.07-3.75 (m, 7H), 3.69-3.43 (m, 6H), 3.12-2.97 (m, 3H), 2.87 (br d, J=11.9 Hz, 1H), 1.49 (d, J=6.2 Hz, 3H).

Example 2

5-[(4R,11aS)-8-[2-[(3S)-3-hydroxypyrrolidin-1-yl]ethylamino]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0156] ##STR00024##

[0157] The title compound was prepared in analogy to the preparation of Example 1 by using (3S)-1-(2-aminoethyl)pyrrolidin-3-ol (CAS: 540787-75-5, Bide Pharmatech, Catalog: BD45313) instead of tert-butyl N-(1,4-oxazepan-6-yl)carbamate in step (a). Example 2 was obtained. MS: calc'd 483 [(M+H).sup.+], measured 483 [(M+H).sup.+]. .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ ppm 9.05-8.98 (m, 1H), 8.73-8.64 (m, 1H), 8.20 (d, J=7.9 Hz, 1H), 7.72-7.63 (m, 1H), 7.35 (d, J=8.1 Hz, 1H), 7.03 (d, J=8.3 Hz, 1H), 6.83-6.63 (m, 1H), 6.58 (d, J=2.2 Hz, 1H), 4.67 (d, J=15.4 Hz, 1H), 4.63-4.56 (m, 1H), 4.00 (d, J=15.2 Hz, 1H), 3.83-3.74 (m, 1H), 3.72-3.60 (m, 3H), 3.59-3.40 (m, 8H), 3.14-2.94 (m, 3H), 2.88 (br d, J=11.5 Hz, 1H), 2.35-2.19 (m, 1H), 2.15-2.02 (m, 1H), 1.50 (d, J=6.4 Hz, 3H).

Example 3

5-[(4R,11aS)-4-methyl-8-[[(2R)-morpholin-2-yl]methylamino]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0158] ##STR00025##

[0159] The title compound was prepared in analogy to the preparation of Example 1 by using tert-butyl (2S)-2-(aminomethyl)morpholine-4-carboxylate (CAS: 879403-42-6, PharmaBlock, Catalog: PBN20121306) instead of tert-butyl N-(1,4-oxazepan-6-yl)carbamate in step (a). Example 3 was obtained. MS: calc'd 469 [(M+H).sup.+], measured 469 [(M+H).sup.+]. .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ ppm 9.09-8.97 (m, 1H), 8.77-8.64 (m, 1H), 8.21 (d, J=7.9 Hz, 1H), 7.79-7.58 (m, 1H), 7.39 (d, J=8.1 Hz, 1H), 7.03 (d, J=8.4 Hz, 1H), 6.75-6.64 (m, 1H), 6.57 (d, J=2.2 Hz, 1H), 4.87 (br d, J=15.5 Hz, 1H), 4.36 (d, J=15.4 Hz, 1H), 4.18-4.05 (m, 2H), 4.02-3.70 (m, 5H), 3.43 (br d, J=12.5 Hz, 1H), 3.32-2.90 (m, 9H), 1.62 (d, J=6.5 Hz, 3H)

Example 4

5-[(4R,11aS)-8-[[(3S,4R)-4-fluoropyrrolidin-3-yl]amino]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0160] ##STR00026##

[0161] The title compound was prepared in analogy to the preparation of Example 1 by using tert-butyl (3S,4R)-3-amino-4-fluoro-pyrrolidine-1-carboxylate (CAS: 1174020-30-4, PharmaBlock, Catalog: PB07374) instead of tert-butyl N-(1,4-oxazepan-6-yl)carbamate in step (a). Example 4 was obtained. MS: calc'd 457 [(M+H).sup.+], measured 457 [(M+H).sup.+]. .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ ppm 9.09-8.98 (m, 1H), 8.74-8.65 (m, 1H), 8.19 (d, J=7.9 Hz, 1H), 7.72-7.65 (m, 1H), 7.34 (d, J=8.1 Hz, 1H), 7.03 (d, J=8.4 Hz, 1H), 6.79-6.71 (m, 1H), 6.65 (d, J=2.0 Hz, 1H), 5.44-5.22 (m, 1H), 4.61 (d, J=15.2 Hz, 1H), 4.52-4.38 (m, 1H), 3.92 (br d, J=15.2 Hz, 1H), 3.84-3.37 (m, 7H), 3.24 (t, J=11.2 Hz, 1H), 3.12-2.94 (m, 3H), 2.86 (br d, J=11.7 Hz, 1H), 1.47 (d, J=6.2 Hz, 3H).

Example 5

5-[(4R,11aS)-8-[2-(dimethylamino)ethoxy]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0162] ##STR00027##

[0163] The title compound was prepared in analogy to the preparation of Example 1 by using 2-(dimethylamino)ethanol (CAS: 108-01-0, Sigma-Aldrich, Catalog: 38990) instead of tert-butyl N-(1,4-oxazepan-6-yl)carbamate in step (a). Example 5 was obtained. MS: calc'd 442 [(M+H).sup.+], measured 442 [(M+H).sup.+]. .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ ppm 8.89-8.81 (m, 1H), 8.60-8.45 (m, 1H), 8.04 (d, J=7.9 Hz, 1H), 7.60-7.47 (m, 1H), 7.17 (d, J=8.1 Hz, 1H), 7.00 (d, J=8.6 Hz, 1H), 6.81-6.71 (m, 2H), 4.42 (d, J=15.5 Hz, 1H), 4.24-4.15 (m, 2H), 3.68-3.53 (m, 2H), 3.50-3.38 (m, 3H), 3.12-3.02 (m, 1H), 2.90-2.76 (m, 4H), 2.86 (s, 6H), 2.72-2.61 (m, 1H), 1.27 (d, J=6.4 Hz, 3H).

Example 6

5-[(4R,11aS)-4-methyl-9-[[(3R,4S)-4-fluoropyrrolidin-3-yl]amino]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0164] ##STR00028##

[0165] The title compound was prepared in analogy to the preparation of Example 1 by using tert-butyl (3R,4S)-3-amino-4-fluoro-pyrrolidine-1-carboxylate (CAS: 1009075-48-2, PharmaBlock, Catalog: PB07375) instead of tert-butyl N-(1,4-oxazepan-6-yl)carbamate and 5-[(4R,11aS)-9-bromo-1,1,1,1,1,4-hexamethyl-4,6,11,11a-tetrahydro-3H-pyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile (Intermediate C) instead of 5-[(4R,11aS)-8-bromo-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile (Intermediate B) in step (a). Example 6 was obtained. MS: calc'd 457 [(M+H).sup.+], measured 457 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 8.92 (dd, 1H, J=1.5, 4.3 Hz), 8.60 (dd, 1H, J=1.5, 8.6 Hz), 8.10 (d, 1H, J=7.9 Hz), 7.59 (dd, 1H, J=4.3, 8.6 Hz), 7.29 (d, 1H, J=7.9 Hz), 7.02 (d, 1H, J=8.6 Hz), 6.66 (dd, 1H, J=2.1, 8.4 Hz), 6.54 (d, 1H, J=1.8 Hz), 5.1-5.4 (m, 1H), 4.80 (br d, 1H, J=15.0 Hz), 4.3-4.4 (m, 1H), 4.22 (br d, 1H, J=15.0 Hz), 4.04 (br t, 1H, J=10.9 Hz), 3.8-3.9 (m, 2H), 3.4-3.8 (m, 4H), 3.0-3.2 (m, 4H), 2.8-3.0 (m, 1H), 1.50 (d, 3H, J=6.5 Hz).

Example 7

5-[(4R,11aS)-9-[[(3R,4S)-4-methoxypyrrolidin-3-yl]amino]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0166] ##STR00029##

[0167] The title compound was prepared in analogy to the preparation of Example 6 by using tert-butyl (3R,4S)-3-amino-4-methoxy-pyrrolidine-1-carboxylate (CAS: 148260-94-0, BePharm, Catalog: BD285562) instead of tert-butyl (3R,4S)-3-amino-4-fluoro-pyrrolidine-1-carboxylate in step (a). Example 7 was obtained. MS: calc'd 469 [(M+H).sup.+], measured 469 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.06 (dd, 1H, J=1.6, 4.3 Hz), 8.73 (dd, 1H, J=1.6, 8.6 Hz), 8.25 (d, 1H, J=7.9 Hz), 7.72 (dd, 1H, J=4.3, 8.6 Hz), 7.42 (d, 1H, J=7.9 Hz), 7.14 (d, 1H, J=8.4 Hz), 6.77 (dd, 1H, J=2.3, 8.4 Hz), 6.64 (d, 1H, J=2.0 Hz), 4.93 (br d, 1H, J=14.1 Hz), 4.3-4.4 (m, 2H), 4.1-4.2 (m, 2H), 4.0-4.0 (m, 1H), 3.9-4.0 (m, 1H), 3.8-3.9 (m, 1H), 3.6-3.7 (m, 2H), 3.42 (s, 3H), 3.1-3.3 (m, 5H), 3.0-3.1 (m, 1H), 1.62 (d, 3H, J=6.5 Hz)

Example 8

5-[(4R,11aS)-9-[(3S,4R)-3-amino-4-fluoro-pyrrolidin-1-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0168] ##STR00030##

[0169] The title compound was prepared in analogy to the preparation of Example 6 by using tert-butyl N-[(3S,4R)-4-fluoropyrrolidin-3-yl]carbamate (CAS: 1033718-89-6, PharmaBlock, Catalog: PB09206) instead of tert-butyl (3R,4S)-3-amino-4-fluoro-pyrrolidine-1-carboxylate in step (a). Example 8 was obtained. MS: calc'd 457 [(M+H).sup.+], measured 457 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ ppm 9.06 (dd, 1H, J=1.6, 4.3 Hz), 8.73 (dd, 1H, J=1.7, 8.6 Hz), 8.24 (d, 1H, J=7.9 Hz), 7.72 (dd, 1H, J=4.2, 8.5 Hz), 7.41 (d, 1H, J=8.1 Hz), 7.21 (d, 1H, J=8.7 Hz), 6.66 (dd, 1H, J=2.3, 8.3 Hz), 6.51 (d, 1H, J=1.7 Hz), 5.3-5.6 (m, 1H), 4.0-4.4 (m, 3H), 3.7-4.0 (m, 6H), 3.4-3.5 (m, 3H), 3.1-3.3 (m, 2H), 3.0-3.1 (m, 1H), 1.59 (br d, 3H, J=6.5 Hz)

Example 9

5-[(4R,11aS)-9-[(3R,4S)-3-amino-4-methoxy-pyrrolidin-1-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0170] ##STR00031##

[0171] The title compound was prepared in analogy to the preparation of Example 6 by using tert-butyl N-[(3R,4S)-4-methoxypyrrolidin-3-yl]carbamate (CAS: 1932508-77-4, PharmaBlock, Catalog: PBZ4729) instead of tert-butyl (3R,4S)-3-amino-4-fluoro-pyrrolidine-1-carboxylate in step (a). Example 9 was obtained. MS: calc'd 469 [(M+H).sup.+], measured 469 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.06 (dd, 1H, J=1.6, 4.3 Hz), 8.73 (dd, 1H, J=1.6, 8.6 Hz), 8.24 (d, 1H, J=7.9 Hz), 7.72 (dd, 1H, J=4.3, 8.6 Hz), 7.41 (d, 1H, J=7.9 Hz), 7.19 (d, 1H, J=8.4 Hz), 6.64 (dd, 1H, J=1.8, 8.8 Hz), 6.49 (d, 1H, J=1.6 Hz), 4.7-4.8 (m, 1H), 4.2-4.3 (m, 1H), 4.1-4.2 (m, 1H), 4.0-4.1 (m, 1H), 3.9-4.0 (m, 1H), 3.8-3.9 (m, 1H), 3.8-3.8 (m, 1H), 3.6-3.7 (m, 1H), 3.5-3.6 (m, 1H), 3.4-3.5 (m, 2H), 3.4-3.4 (m, 3H), 3.32 (dd, 1H, J=6.7, 9.8 Hz), 3.0-3.2 (m, 3H), 2.9-3.0 (m, 1H), 1.4-1.6 (m, 3H)

Example 10

5-[(4R,11aS)-9-[(4aS,7aS)-3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazin-6-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0172] ##STR00032##

[0173] The title compound was prepared in analogy to the preparation of Example 6 by using tert-butyl (4aR,7aR)-3,4a,5,6,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazine-4-carboxylate (CAS: 1932337-68-2, PharmaBlock, Catalog: PBXA8123) instead of tert-butyl (3R,4S)-3-amino-4-fluoro-pyrrolidine-1-carboxylate in step (a). Example 10 was obtained. MS: calc'd 481 [(M+H).sup.+], measured 481 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.06 (dd, 1H, J=1.5, 4.2 Hz), 8.73 (dd, 1H, J=1.7, 8.6 Hz), 8.25 (d, 1H, J=7.9 Hz), 7.72 (dd, 1H, J=4.3, 8.7 Hz), 7.42 (d, 1H, J=7.9 Hz), 7.20 (d, 1H, J=8.6 Hz), 6.64 (dd, 1H, J=2.2, 8.8 Hz), 6.48 (d, 1H, J=2.4 Hz), 4.90 (br d, 1H, J=15.0 Hz), 4.36 (br d, 1H, J=15.0 Hz), 4.28 (dd, 1H, J=3.9, 13.4 Hz), 3.9-4.2 (m, 5H), 3.7-3.9 (m, 3H), 3.4-3.7 (m, 4H), 3.0-3.3 (m, 5H), 1.62 (d, 3H, J=6.5 Hz)

Example 11

5-[(4R,11aS)-9-[2-(dimethylamino)ethoxy]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0174] ##STR00033##

[0175] The title compound was prepared in analogy to the preparation of Example 6 by using 2-(dimethylamino)ethanol instead of tert-butyl (3R,4S)-3-amino-4-fluoro-pyrrolidine-1-carboxylate in step (a). Example 11 was obtained. MS: calc'd 442 [(M+H).sup.+], measured 442 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.03 (dd, 1H, J=1.5, 4.3 Hz), 8.72 (dd, 1H, J=1.5, 8.7 Hz), 8.22 (d, 1H, J=7.9 Hz), 7.71 (dd, 1H, J=4.2, 8.6 Hz), 7.41 (d, 1H, J=7.9 Hz), 7.31 (d, 1H, J=8.7 Hz), 7.04 (dd, 1H, J=2.4, 8.6 Hz), 6.96 (d, 1H, J=2.2 Hz), 5.00 (br d, 1H, J=15.3 Hz), 4.3-4.5 (m, 3H), 4.19 (br t, 1H, J=10.3 Hz), 3.9-4.1 (m, 2H), 3.80 (br d, 1H, J=13.3 Hz), 3.5-3.7 (m, 2H), 3.2-3.3 (m, 3H), 3.13 (br dd, 1H, J=11.9, 17.7 Hz), 3.01 (s, 6H), 1.64 (d, 3H, J=6.5 Hz)

Example 12

5-[(4R,11aS)-9-[[(2S)-azetidin-2-yl]methoxy]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0176] ##STR00034##

[0177] The title compound was prepared in analogy to the preparation of Example 6 by using tert-butyl (2S)-2-(hydroxymethyl)azetidine-1-carboxylate (CAS: 161511-85-9, PharmaBlock, Catalog: PB03034) instead of tert-butyl (3R,4S)-3-amino-4-fluoro-pyrrolidine-1-carboxylate in step (a). Example 12 was obtained. MS: calc'd 440 [(M+H).sup.+], measured 440 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.06 (dd, 1H, J=1.7, 4.2 Hz), 8.73 (dd, 1H, J=1.6, 8.6 Hz), 8.25 (d, 1H, J=7.9 Hz), 7.73 (dd, 1H, J=4.3, 8.6 Hz), 7.43 (d, 1H, J=8.1 Hz), 7.33 (d, 1H, J=8.7 Hz), 7.07 (dd, 1H, J=2.4, 8.5 Hz), 6.98 (d, 1H, J=2.3 Hz), 5.01 (br d, 1H, J=15.0 Hz), 4.41 (br d, 1H, J=15.0 Hz), 4.35 (d, 2H, J=4.6 Hz), 3.9-4.3 (m, 6H), 3.8-3.9 (m, 1H), 3.1-3.3 (m, 4H), 2.6-2.8 (m, 2H), 1.63 (d, 3H, J=6.5 Hz).

Example 13

5-[(4R,11aS)-4-methyl-9-[[(3R,4S)-4-fluoropyrrolidin-3-yl]amino]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0178] ##STR00035##

[0179] The titled compound was synthesized according to the following scheme:

##STR00036## ##STR00037##

Step (a): Preparation of Tert-Butyl 4-[(4R,11aS)-2-(8-cyano-5-quinolyl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-9-yl]piperazine-1-carboxylate (Compound 13.1)

[0180] To a solution of tert-butyl piperazine-1-carboxylate (60 mg, 322 μmol) in dioxane (5 mL) was added 5-((4R,11aS)-9-bromo-4-methyl-1,3,4,6,11,11a-hexahydro-2H-pyrazino[1,2-b]isoquinolin-2-yl) quinoline-8-carbonitrile (Intermediate C, 139.4 mg, 277 μmol), tBuONa (61.9 mg, 644 μmol) and tBuXPhos Pd G3 (CAS: 1447963-75-8, Sigma-Aldrich, Catalog: 762229, 25.6 mg, 32.2 μmol). The resultant mixture was stirred at 90° C. overnight. After being cooled to room temperature, the mixture was diluted with water (20 mL), and extracted with EA (20 mL) for three times. The combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica gel, 24 g, 0% to 100% EtOAc in PE) to afford compound 13.1 (26.1 mg, 35% yield). MS: calc'd 539 [(M+H).sup.+], measured 539 [(M+H).sup.+].

Step (b): Preparation of 5-[(4R,11aS)-4-methyl-9-piperazin-1-yl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile (Compound 13.2)

[0181] To a solution of tert-butyl 4-[(4R,11aS)-2-(8-cyano-5-quinolyl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-9-yl]piperazine-1-carboxylate (compound 13.1, 26.1 mg, 48.5 μmol) in DCM (2 mL) was added TFA (1 mL). The reaction mixture was stirred at room temperature for 30 min, quenched with saturated aq.NaHCO.sub.3, washed with brine and dried over Na.sub.2SO.sub.4, then concentrated to afford compound 13.2 (20.2 mg, 95% yield). MS: calc'd 439 [(M+H).sup.+], measured 439 [(M+H).sup.+].

Step (c): Preparation of Tert-Butyl N-[1,1-dimethyl-2-oxo-2-[4-[(4R,11aS)-2-(8-cyano-5-quinolyl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-9-yl]piperazin-1-yl]ethyl]carbamate (Compound 13.3)

[0182] To a solution of 5-[(4R,11aS)-4-methyl-9-piperazin-1-yl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile (compound 13.2, 26.1 mg, 48.5 μmol), 2-(tert-butoxycarbonylamino)-2-methyl-propanoic acid (CAS: 30992-29-1, Sigma-Aldrich, Catalog: 15466, 11.8 mg, 58.2 μmol) and HATU in DMF (5 mL) was added DIEA (18.8 mg, 145.5 μmol). The reaction mixture was stirred at room temperature for 2 hrs, then quenched with water, extracted with EA. The organic layer was washed with brine, dried over Na.sub.2SO.sub.4, and then concentrated in vacuo to afford compound 13.3 (29.7 mg, 80% yield). MS: calc'd 624 [(M+H).sup.+], measured 624 [(M+H).sup.+].

Step (d): Preparation of 5-[(4R,11aS)-9-[4-(2-amino-2-methyl-propanoyl)piperazin-1-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile (Example 13)

[0183] To a solution of tert-butyl N-[1,1-dimethyl-2-oxo-2-[4-[(4R,11aS)-2-(8-cyano-5-quinolyl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-9-yl]piperazin-1-yl]ethyl]carbamate (compound 13.3, 29.7 mg, 47.7 μmol) in DCM (2 mL) was added TFA (1 mL). The reaction mixture was stirred at room temperature for 30 min, then concentrated to afford a crude product, which was purified by prep-HPLC to afford Example 13 (11.9 mg, 48% yield). MS: calc'd 524 [(M+H).sup.+], measured 524 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.00 (dd, 1H, J=1.6, 4.3 Hz), 8.68 (dd, 1H, J=1.7, 8.6 Hz), 8.18 (d, 1H, J=8.1 Hz), 7.67 (dd, 1H, J=4.2, 8.6 Hz), 7.30 (d, 1H, J=8.1 Hz), 7.08 (d, 1H, J=8.4 Hz), 6.88 (dd, 1H, J=2.3, 8.3 Hz), 6.77 (d, 1H, J=2.1 Hz), 4.35 (d, 1H, J=14.8 Hz), 3.92 (br s, 4H), 3.6-3.7 (m, 1H), 3.49 (dd, 1H, J=2.1, 9.1 Hz), 3.40 (d, 1H, J=14.7 Hz), 3.1-3.2 (m, 4H), 3.0-3.1 (m, 1H), 2.8-3.0 (m, 4H), 2.7-2.8 (m, 1H), 1.47 (s, 6H), 1.32 (d, 3H, J=5.6 Hz)

Example 14

5-[(4R,11aS)-4-methyl-9-[4-[(2S)-2-methylpyrrolidine-2-carbonyl]piperazin-1-yl]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0184] ##STR00038##

[0185] The title compound was prepared in analogy to the preparation of Example 13 by using (2S)-1-tert-butoxycarbonyl-2-methyl-pyrrolidine-2-carboxylic acid (CAS: 103336-06-7, PharmaBlock, Catalog: PBN20121551) instead of 2-(tert-butoxycarbonylamino)-2-methyl-propanoic acid in step (c). Example 14 was obtained. MS: calc'd 550 [(M+H).sup.+], measured 550 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.05 (dd, 1H, J=1.6, 4.3 Hz), 8.73 (dd, 1H, J=1.7, 8.6 Hz), 8.24 (d, 1H, J=7.9 Hz), 7.72 (dd, 1H, J=4.2, 8.6 Hz), 7.42 (d, 1H, J=8.1 Hz), 7.24 (d, 1H, J=8.6 Hz), 7.03 (dd, 1H, J=2.3, 8.6 Hz), 6.89 (d, 1H, J=2.2 Hz), 4.96 (d, 1H, J=15.2 Hz), 4.39 (br d, 1H, J=15.2 Hz), 4.1-4.3 (m, 1H), 3.9-4.0 (m, 2H), 3.7-3.9 (m, 5H), 3.4-3.5 (m, 2H), 3.2-3.3 (m, 7H), 3.0-3.2 (m, 1H), 2.3-2.5 (m, 2H), 2.0-2.3 (m, 2H), 1.76 (s, 3H), 1.6-1.7 (m, 3H).

Example 15

5-[(4R,11aS)-9-[(1S,4S)-5-(2-amino-2-methyl-propanoyl)-2,5-diazabicyclo[2.2.1]heptan-2-yl]-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0186] ##STR00039##

[0187] The title compound was prepared in analogy to the preparation of Example 13 by using tert-butyl (1S,4S)-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate (CAS: 113451-59-5, PharmaBlock, Catalog: PBN20120579) instead of tert-butyl piperazine-1-carboxylate in step (a). Example 15 was obtained. MS: calc'd 536 [(M+H).sup.+], measured 536 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.07 (dd, 1H, J=1.6, 4.3 Hz), 8.78 (br d, 1H, J=8.6 Hz), 8.26 (d, 1H, J=7.8 Hz), 7.6-7.9 (m, 1H), 7.44 (d, 1H, J=7.7 Hz), 7.18 (d, 1H, J=8.7 Hz), 6.69 (dd, 1H, J=2.3, 8.6 Hz), 6.55 (br s, 1H), 5.03 (s, 1H), 4.90 (br, d, 1H, J=14.9 Hz), 4.6-4.7 (m, 1H), 4.36 (d, 1H, J=14.9 Hz), 4.1-4.2 (m, 1H), 3.9-4.1 (m, 2H), 3.4-3.8 (m, 4H), 3.2-3.3 (m, 3H), 3.1-3.2 (m, 2H), 2.0-2.2 (m, 2H), 1.71 (br s, 6H), 1.63 (d, 3H, J=6.5 Hz).

Example 16

5-[(4R,11aS)-9-(4-amino-2-oxo-pyrrolidin-1-yl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0188] ##STR00040##

[0189] The titled compound was synthesized according to the following scheme:

##STR00041##

Step (a): Preparation of Tert-Butyl N-[5-oxo-1-[(4R,11aS)-2-(8-cyano-5-quinolyl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-9-yl]pyrrolidin-3-yl]carbamate (Compound 16.1)

[0190] To a solution of tert-butyl N-(5-oxopyrrolidin-3-yl)carbamate (CAS: 1245648-84-3, BePharm, Catalog: BD165019, 60 mg, 299 μmol) in dioxane (5 mL) was added 5-((4R,11aS)-8-bromo-4-methyl-1,3,4,6,11,11a-hexahydro-2H-pyrazino[1,2-b]isoquinolin-2-yl)quinoline-8-carbonitrile (Intermediate C, 129.6 mg, 299 μmol), Cs.sub.2CO.sub.3 (136.4 mg, 418.6 μmol) and Pd.sub.2(dba).sub.3 (13.7 mg, 14.9 μmol) and Xantphos (CAS: 51364-51-3, Sigma-Aldrich, Catalog: 526460, 25.9 mg, 44.7 μmol). The resultant mixture was stirred at 120° C. overnight. After being cooled to room temperature, the mixture was diluted with water (20 mL), and extracted with EA (20 mL) for three times. The combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica gel, 24 g, 0% to 100% EtOAc in PE) to afford compound 16.1 (76.5 mg, 79% yield). MS: calc'd 553 [(M+H).sup.+], measured 553 [(M+H).sup.+].

Step (b): Preparation of 5-[(4R,11aS)-9-(4-amino-2-oxo-pyrrolidin-1-yl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile (Example 16)

[0191] To a solution of tert-butyl N-[5-oxo-1-[(4R,11aS)-2-(8-cyano-5-quinolyl)-4-methyl-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-9-yl]pyrrolidin-3-yl]carbamate (compound 16.1, 76.5 mg, 138.4 μmol) in DCM (2 mL) was added TFA (1 mL). The reaction mixture was stirred at room temperature for 30 min, then concentrated to afford a crude product, which was purified by prep-HPLC to afford Example 16 (28.3 mg, 45.1% yield). MS: calc'd 453 [(M+H).sup.+], measured 453 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.06 (dd, 1H, J=1.5, 4.3 Hz), 8.73 (dd, 1H, J=1.6, 8.7 Hz), 8.25 (d, 1H, J=7.9 Hz), 7.5-7.9 (m, 3H), 7.3-7.5 (m, 2H), 5.07 (br d, 1H, J=15.4 Hz), 4.3-4.6 (m, 2H), 4.1-4.3 (m, 2H), 3.9-4.1 (m, 3H), 3.82 (br d, 1H, J=12.7 Hz), 3.1-3.3 (m, 5H), 2.69 (dd, 1H, J=3.3, 18.0 Hz), 1.64 (d, 3H, J=6.5 Hz)

Example 17A and 17B

5-[(4R,11aS)-4-methyl-9-[(8aS)-3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile and 5-[(4R,11aS)-4-methyl-9-[(8aR)-3-oxo-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyrazin-2-yl]-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0192] ##STR00042##

[0193] The title compounds were prepared according to the following scheme:

##STR00043##

[0194] The compound 17.1 was prepared in analogy to the preparation of Example 16 by using tert-butyl 3-oxo-1,2,5,6,8,8a-hexahydroimidazo[1,5-a]pyrazine-7-carboxylate (CAS: 1246551-25-6, BePharm, Catalog: BD286163) instead of tert-butyl N-(5-oxopyrrolidin-3-yl)carbamate in step (a). Then Compound 17.1 was resolved by SFC to give two single isomers: Example 17A (faster eluting) and Example 17B (slower eluting) with 30% methanol (0.1% NH.sub.3H.sub.2O)/CO.sub.2 on DAICEL CHIRALPAK AD (10 μm, 250×30 mm) column.

[0195] Example 17A MS: calc'd 494 [(M+H).sup.+], measured 494 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 8.92 (dd, 1H, J=1.2, 4.2 Hz), 8.61 (dd, 1H, J=1.3, 8.6 Hz), 8.11 (d, 1H, J=8.1 Hz), 7.60 (dd, 1H, J=4.3, 8.6 Hz), 7.44 (s, 2H), 7.30 (d, 1H, J=7.9 Hz), 7.21 (d, 1H, J=9.0 Hz), 4.90 (br d, 1H, J=15.4 Hz), 4.33 (br d, 1H, J=15.4 Hz), 3.6-4.2 (m, 8H), 3.5-3.6 (m, 1H), 3.44 (br d, 1H, J=12.3 Hz), 3.31 (br d, 1H, J=12.6 Hz), 3.23 (br d, 1H, J=3.8 Hz), 3.1-3.2 (m, 3H), 2.9-3.1 (m, 3H), 1.52 (d, 3H, J=6.5 Hz).

[0196] Example 17B MS: calc'd 494 [(M+H).sup.+], measured 494 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.06 (dd, 1H, J=1.5, 4.2 Hz), 8.73 (dd, 1H, J=1.7, 8.6 Hz), 8.25 (d, 1H, J=7.9 Hz), 7.73 (dd, 1H, J=4.3, 8.6 Hz), 7.5-7.6 (m, 2H), 7.43 (d, 1H, J=7.9 Hz), 7.34 (d, 1H, J=8.9 Hz), 5.02 (br d, 1H, J=15.8 Hz), 4.44 (br d, 1H, J=15.4 Hz), 4.1-4.3 (m, 6H), 3.9-4.1 (m, 2H), 3.7-3.9 (m, 2H), 3.4-3.6 (m, 2H), 3.0-3.3 (m, 6H), 1.63 (d, 3H, J=6.4 Hz).

Example 18

5-[(4R,11aS)-4-methyl-9-(3-oxo-3a,4,5,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridin-2-yl)-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0197] ##STR00044##

[0198] The title compound was prepared in analogy to the preparation of Example 16 by using tert-butyl 3-oxo-2,3a,4,6,7,7a-hexahydro-1H-pyrrolo[3,4-c]pyridine-5-carboxylate (CAS: 1780976-05-7, PharmaBlock, Catalog: PBWBD0104) instead of tert-butyl N-(5-oxopyrrolidin-3-yl)carbamate in in step (a). Example 18 was obtained. MS: calc'd 493 [(M+H).sup.+], measured 493 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.06 (d, 1H, J=4.2 Hz), 8.73 (dd, 1H, J=1.6, 8.6 Hz), 8.25 (d, 1H, J=8.1 Hz), 7.6-7.8 (m, 3H), 7.41 (dd, 2H, J=8.2, 15.8 Hz), 5.06 (br d, 1H, J=15.9 Hz), 4.47 (br d, 1H, J=15.7 Hz), 4.2-4.3 (m, 1H), 4.12 (td, 1H, J=4.9, 10.1 Hz), 3.9-4.1 (m, 2H), 3.82 (br d, 1H, J=13.3 Hz), 3.5-3.6 (m, 2H), 3.4-3.4 (m, 1H), 3.1-3.3 (m, 5H), 2.8-3.0 (m, 3H), 2.39 (br dd, 1H, J=1.8, 15.2 Hz), 2.0-2.2 (m, 1H), 1.64 (d, 3H, J=6.5 Hz).

Example 19

5-[(4R,11aS)-4-methyl-9-(1-oxo-3a,4,5,6,7,7a-hexahydro-3H-pyrrolo[3,4-c]pyridin-2-yl)-1,3,4,6,11,11a-hexahydropyrazino[1,2-b]isoquinolin-2-yl]quinoline-8-carbonitrile

[0199] ##STR00045##

[0200] The title compound was prepared in analogy to the preparation of Example 16 by using tert-butyl 1-oxo-3,3a,4,6,7,7a-hexahydro-2H-pyrrolo[3,4-c]pyridine-5-carboxylate (CAS: 1781135-05-4, PharmaBlock, Catalog: PBWBD0105) instead of tert-butyl N-(5-oxopyrrolidin-3-yl)carbamate in in step (a). Example 19 was obtained. MS: calc'd 493 [(M+H).sup.+], measured 493 [(M+H).sup.+]. .sup.1H NMR (METHANOL-d.sub.4, 400 MHz) δ 9.06 (d, 1H, J=4.0 Hz), 8.73 (d, 1H, J=8.6 Hz), 8.25 (d, 1H, J=7.8 Hz), 7.6-7.8 (m, 3H), 7.41 (dd, 2H, J=8.4, 15.8 Hz), 5.05 (br d, 1H, J=15.3 Hz), 4.46 (br d, 1H, J=15.5 Hz), 4.1-4.3 (m, 2H), 3.9-4.1 (m, 2H), 3.82 (br d, 2H, J=13.1 Hz), 3.58 (br dd, 2H, J=4.0, 10.2 Hz), 3.0-3.3 (m, 8H), 2.7-2.9 (m, 1H), 2.1-2.2 (m, 1H), 1.64 (d, 3H, J=6.5 Hz).

Example 20

[0201] The following tests were carried out in order to determine the activity of the compounds of formula (I), (Ia) or (Ib) in HEK293-Blue-hTLR-7/8/9 cells assay.

[0202] HEK293-Blue-hTLR-7 Cells Assay:

[0203] A stable HEK293-Blue-hTLR-7 cell line was purchased from InvivoGen (Cat.#: hkb-htlr7, San Diego, Calif., USA). These cells were originally designed for studying the stimulation of human TLR7 by monitoring the activation of NF-κB. A SEAP (secreted embryonic alkaline phosphatase) reporter gene was placed under the control of the IFN-β minimal promoter fused to five NF-κB and AP-1-binding sites. The SEAP was induced by activating NF-κB and AP-1 via stimulating HEK-Blue hTLR7 cells with TLR7 ligands. Therefore the reporter expression was declined by TLR7 antagonist under the stimulation of a ligand, such as R848 (Resiquimod), for incubation of 20 hrs. The cell culture supernatant SEAP reporter activity was determined using QUANTI-Blue™ kit (Cat.#: rep-qb1, Invivogen, San Diego, Ca, USA) at a wavelength of 640 nm, a detection medium that turns purple or blue in the presence of alkaline phosphatase.

[0204] HEK293-Blue-hTLR7 cells were incubated at a density of 250,000˜450,000 cells/mL in a volume of 170 μL in a 96-well plate in Dulbecco's Modified Eagle's medium (DMEM) containing 4.5 g/L glucose, 50 U/mL penicillin, 50 mg/mL streptomycin, 100 mg/mL Normocin, 2 mM L-glutamine, 10% (v/v) heat-inactivated fetal bovine serum with addition of 20 μL test compound in a serial dilution in the presence of final DMSO at 1% and 10 μL of 20 uM R848 in above DMEM, perform incubation under 37° C. in a CO.sub.2 incubator for 20 hrs. Then 20 μL of the supernatant from each well was incubated with 180 μL Quanti-blue substrate solution at 37° C. for 2 hrs and the absorbance was read at 620-655 nm using a spectrophotometer. The signaling pathway that TLR7 activation leads to downstream NF-κB activation has been widely accepted, and therefore similar reporter assay was modified for evaluating TLR7 antagonist.

[0205] HEK293-Blue-hTLR-8 Cells Assay:

[0206] A stable HEK293-Blue-hTLR-8 cell line was purchased from InvivoGen (Cat.#: hkb-htlr8, San Diego, Calif., USA). These cells were originally designed for studying the stimulation of human TLR8 by monitoring the activation of NF-κB. A SEAP (secreted embryonic alkaline phosphatase) reporter gene was placed under the control of the IFN-β minimal promoter fused to five NF-κB and AP-1-binding sites. The SEAP was induced by activating NF-κB and AP-1 via stimulating HEK-Blue hTLR8 cells with TLR8 ligands. Therefore the reporter expression was declined by TLR8 antagonist under the stimulation of a ligand, such as R848, for incubation of 20 hrs. The cell culture supernatant SEAP reporter activity was determined using QUANTI-Blue™ kit (Cat.#: rep-qb1, Invivogen, San Diego, Ca, USA) at a wavelength of 640 nm, a detection medium that turns purple or blue in the presence of alkaline phosphatase.

[0207] HEK293-Blue-hTLR8 cells were incubated at a density of 250,000-450,000 cells/mL in a volume of 170 μL in a 96-well plate in Dulbecco's Modified Eagle's medium (DMEM) containing 4.5 g/L glucose, 50 U/mL penicillin, 50 mg/mL streptomycin, 100 mg/mL Normocin, 2 mM L-glutamine, 10% (v/v) heat-inactivated fetal bovine serum with addition of 20 μL test compound in a serial dilution in the presence of final DMSO at 1% and 10 μL of 60 uM R848 in above DMEM, perform incubation under 37° C. in a CO.sub.2 incubator for 20 hrs. Then 20 μL of the supernatant from each well was incubated with 180 μL Quanti-blue substrate solution at 37° C. for 2 hrs and the absorbance was read at 620˜655 nm using a spectrophotometer. The signaling pathway that TLR8 activation leads to downstream NF-κB activation has been widely accepted, and therefore similar reporter assay was modified for evaluating TLR8 antagonist.

[0208] HEK293-Blue-hTLR-9 Cells Assay:

[0209] A stable HEK293-Blue-hTLR-9 cell line was purchased from InvivoGen (Cat.#: hkb-htlr9, San Diego, Calif., USA). These cells were originally designed for studying the stimulation of human TLR9 by monitoring the activation of NF-κB. A SEAP (secreted embryonic alkaline phosphatase) reporter gene was placed under the control of the IFN-β minimal promoter fused to five NF-κB and AP-1-binding sites. The SEAP was induced by activating NF-κB and AP-1 via stimulating HEK-Blue hTLR9 cells with TLR9 ligands. Therefore the reporter expression was declined by TLR9 antagonist under the stimulation of a ligand, such as ODN2006 (Cat.#: tlrl-2006-1, Invivogen, San Diego, Calif., USA), for incubation of 20 hrs. The cell culture supernatant SEAP reporter activity was determined using QUANTI-Blue™ kit (Cat.#: rep-qb1, Invivogen, San Diego, Calif., USA) at a wavelength of 640 nm, a detection medium that turns purple or blue in the presence of alkaline phosphatase.

[0210] HEK293-Blue-hTLR9 cells were incubated at a density of 250,000-450,000 cells/mL in a volume of 170 μL in a 96-well plate in Dulbecco's Modified Eagle's medium (DMEM) containing 4.5 g/L glucose, 50 U/mL penicillin, 50 mg/mL streptomycin, 100 mg/mL Normocin, 2 mM L-glutamine, 10% (v/v) heat-inactivated fetal bovine serum with addition of 20 μL test compound in a serial dilution in the presence of final DMSO at 1% and 10 μL of 20 uM ODN2006 in above DMEM, perform incubation under 37° C. in a CO.sub.2 incubator for 20 hrs. Then 20 μL of the supernatant from each well was incubated with 180 μL Quanti-blue substrate solution at 37° C. for 2 h and the absorbance was read at 620-655 nm using a spectrophotometer. The signaling pathway that TLR9 activation leads to downstream NF-κB activation has been widely accepted, and therefore similar reporter assay was modified for evaluating TLR9 antagonist.

[0211] The compounds of formula (I) have TLR7 and/or TLR8 inhibitory activities (IC.sub.50 value)<0.1 μM. Moreover, most compounds also have TLR9 inhibitory activity<0.3 μM. Activity data of the compounds of the present invention were shown in Table 1.

TABLE-US-00001 TABLE 1 The activity of the compounds of present invention in HEK293-Blue-hTLR-7/8/9 cells assays Example HEK/hTLR7 HEK/hTLR8 HEK/hTLR9 No IC.sub.50 (nM) IC.sub.50 (nM) IC.sub.50 (nM) 1 71.6 14.5 64.6 2 53.1 4.2 44.5 3A 33.2 4.5 77.3 3B 60.7 5.7 103.1 4A 23.2 <3.2 97.5 4B 31.8 7.8 85.5 5 38.2 9.2 96.3 6 24.7 26.1 106.4 7 27.4 13.5 109.0 8 35.5 21.5 85.3 9 19.5 2.3 138.9 10 21.8 1.5 78.2 11 5.8 11.1 81.0 12 18.2 22.9 116.5 13 18.6 37.5 85.6 14 18.6 1.4 254.1 15 2.4 4.7 125.2 16 2.9 5.3 125.4 17A 10.3 8.0 106.7 17B 10.3 2.4 106.4 18 71.6 14.5 64.6 19 53.1 4.2 44.5

Example 21

[0212] Human Microsomal Stability Assay

[0213] Human liver microsomes (Cat.NO.: 452117, Corning, USA) were preincubated with test compound for 10 minutes at 37° C. in 100 mM potassium phosphate buffer, pH 7.4. The reactions were initiated by adding NADPH regenerating system. The final incubation mixtures contained 1 μM test compound, 0.5 mg/mL liver microsomal protein, 1 mM MgCl.sub.2, 1 mM NADP, 1 unit/mL isocitric dehydrogenase and 6 mM isocitric acid in 100 mM potassium phosphate buffer, pH 7.4. After incubation times of 0, 3, 6, 9, 15 and 30 minutes at 37° C., 300 μL of cold ACN (including internal standard) was added to 100 μL incubation mixture to terminate the reaction. Following precipitation and centrifugation, 100 uL supernatant will be taken out and added 300 uL water. The amount of compound remaining in the samples was determined by LC-MS/MS. Controls of no NADPH regenerating system at zero and 30 minutes were also prepared and analyzed. The results were categorized as: low (<7.0 mL/min/kg), medium (7.0-16.2 mL/min/kg) and high (16.2-23.2 mL/min/kg). Test results were summarized in Table 2.

TABLE-US-00002 TABLE 2 Human microsomal stability results Example CL(h) No (mL/min/kg) 6 6.8 8 9.6 9 8.8 10 9.3 13 7.6 14 8.7 16 6.8

[0214] hERG Channel Inhibition Assay

[0215] The hERG channel inhibition assay is a highly sensitive measurement that identifies compounds exhibiting hERG inhibition related to cardiotoxicity in vivo. The hERG K.sup.+ channels were cloned in humans and stably expressed in a CHO (Chinese hamster ovary) cell line. CHO.sub.hERG cells were used for patch-clamp (voltage-clamp, whole-cell) experiments. Cells were stimulated by a voltage pattern to activate hERG channels and conduct I.sub.KhERG Currents (rapid delayed outward rectifier potassium current of the hERG channel). After the cells were stabilized for a few minutes, the amplitude and kinetics of I.sub.KhERG were recorded at a stimulation frequency of 0.1 Hz (6 bpm). Thereafter, the test compound was added to the preparation at increasing concentrations. For each concentration, an attempt was made to reach a steady-state effect, usually, this was achieved within 3-10 min at which time the next highest concentration was applied. The amplitude and kinetics of IKh.sub.ERG are recorded in each concentration of the drug which were compared to the control values (taken as 100%). (references: Redfern W S, Carlsson L, Davis A S, Lynch W G, MacKenzie I, Palethorpe S, Siegl P K, Strang I, Sullivan A T, Wallis R, Camm A J, Hammond T G. 2003; Relationships between preclinical cardiac electrophysiology, clinical QT interval prolongation and torsade de pointes for a broad range of drugs: evidence for a provisional safety margin in drug development. Cardiovasc. Res. 58:32-45, Sanguinetti M C, Tristani-Firouzi M. 2006; hERG potassium channels and cardiac arrhythmia. Nature 440:463-469, Webster R, Leishman D, Walker D. 2002; Towards a drug concentration effect relationship for QT prolongation and torsades de pointes. Curr. Opin. Drug Discov. Devel. 5:116-26). Results of hERG are given in Table 3.

TABLE-US-00003 TABLE 3 hERG results Example hERG hERG No IC.sub.20 (μM) IC.sub.50 (μM) 6 >10 >20 12 8.2 >20 17A >10 >20