Patent Application
20180194773
The present invention relates to a pharmaceutically-useful bicyclic heterocyclic amide derivative including a pharmaceutically acceptable salt thereof, and an anti-tumor agent comprising it as an active ingredient.
Conventional cancer treatments are sometimes not expected to bring in meaningful survival effects even if they can induce the regression of tumors, because of the persistent proliferation of malignant tumors, the metastasis or recurrence of cancer, and the resistance to an anti-tumor agent. These days, it has been suggested that cancer stem cell (hereinafter referred to as “CSC”, as necessary) is one of the reasons of the failure, which is closely involved in the factors such as the persistent proliferation of malignant tumor. CSCs have been identified in almost all types of major cancers in human such as breast cancer, colon cancer, lung cancer, and hematological malignancy (Non-Patent Document 1). Also, CSCs can be greatly different in the biological feature from standard cancer cells which differentiate from CSCs, and thus the development of an anti-tumor agent whose target is CSCs is expected to lead to a new strategy for cancer treatments (Non-Patent Document 2).
One of the features in CSCs is the self-renewal ability (Non-Patent Document 3). Reliable methods established for measuring the self-renewal ability of cells include, for example, a method for measuring the sphere-forming ability of cancer cells in non-adherent condition in the absence of serum (Non-Patent Document 4).
Non-Patent Document 5 discloses that PF-03084014 having an N-imidazolylamide skeleton can inhibit CSCs to exhibit an anti-cancer effect. However, Non-Patent Document 5 does not disclose the compound of formula (1) of the present invention.
Non-Patent Document 1: Boman et al., Journal of Clinical Oncology 26(17): 2795-2799. 2008
Non-Patent Document 2: Lobo et al., Annu Rev Cell Dev Biol 23: 675-99. 2007
Non-Patent Document 3: Al-Hajj et al., Oncogene 23(43): 7274-82. 2004
Non-Patent Document 4: Ponti et al., Cancer Res 65(13): 5506-11. 2005
Non-Patent Document 5: Zhang et al., Stem Cells Translational Medicine 2: 233-242. 2013
An object of the present invention is to provide a novel anti-tumor agent whose target is CSCs which are thought to be closely involved in the persistent proliferation of malignant tumor, the metastasis or recurrence of cancer, and the resistance to an anti-tumor agent.
The present inventors have extensively studied to reach the above object, and then have found that a compound of the following formula (1) or a pharmaceutically acceptable salt thereof (hereinafter referred to as “the present compound”, as necessary) has a potent inhibitory effect on the sphere-forming ability of cancer cells and is highly useful as a novel anti-tumor agent. Based upon the new findings, the present invention has been completed.
The present invention provides inventions described below.
or a pharmaceutically acceptable salt thereof, wherein ring Q1 is optionally-substituted C6-10 aryl group, optionally-substituted C3-10 cycloalkyl group, or optionally-substituted 5- to 10-membered heteroaryl group;
R1 and R2 are independently hydrogen atom, halogen atom, or C1-6 alkyl group which may be optionally substituted with the same or different 1 to 3 halogen atoms;
W1 is optionally-substituted C1-4 alkylene group;
W2-Cy1 is —NR3aC(O)-Cy1, —NR3aC(O)O-Cy1, —NR3aC(O)OCH2-Cy1, —NR3aC(O)NR3b-Cy1, —NR3aC(O)NR3bCH2-Cy1, —NR3aC(O)CH2O-Cy1, —NR3aC(O)CH2-Cy1, —NR3aC(O)CH2CH2-Cy1, —C(O)NR3a-Cy1, —C(O)NR3aCH2—C(O)NR3aCH2CH2-Cy1, or —NR3aC(O)—CR3c═CR3-Cy1 wherein R3a and R3b are independently hydrogen atom or C1-6 alkyl group; and R3c and R3d are independently hydrogen atom, fluorine atom, or C1-6 alkyl group; and
Cy1 is a group of the following formula (11), (12), (13), (14), (15), or (16):
wherein ring Q2 is optionally-substituted benzene ring, optionally-substituted pyridine ring, optionally-substituted pyrimidine ring, optionally-substituted pyridazine ring, or optionally-substituted pyrazine ring;
ring Q3 is optionally-substituted 5-membered heteroaryl ring;
n and m are independently 0, 1 or 2, provided that n and m are not simultaneously 0;
X and Z are independently NR5, —NR3eC(O)—, —C(O)NR3e—, or O wherein R5 is hydrogen atom, C1-6 alkyl group which may be optionally substituted with the same or different 1 to 3 halogen atoms, or C1-6 alkylcarbonyl; and R3e is hydrogen atom or C1-6 alkyl group;
p is 1, 2, 3, 4 or 5; and
R4 is, independently when two or more exist, hydrogen atom, halogen atom, hydroxy, oxo, C1-6 alkyl group which may be optionally substituted with the same or different 1 to 3 halogen atoms, or C1-6 alkoxy group which may be optionally substituted with the same or different 1 to 3 halogen atoms; or
when two R4 are attached to the same carbon atom or the adjacent carbon atoms on the ring, they may be combined with the carbon atom(s) to form
or a pharmaceutically acceptable salt thereof, wherein ring Q1 is optionally-substituted C6-10 aryl group, optionally-substituted C3-10 cycloalkyl group, or optionally-substituted 5- to 10-membered heteroaryl group;
R1 and R2 are independently hydrogen atom, halogen atom, or C1-6 alkyl group which may be optionally substituted with the same or different 1 to 3 halogen atoms;
W1 is optionally-substituted C1-4 alkylene group;
W2-Cy1 is —NR3aC(O)-Cy1, —NR3aC(O)O-Cy1, —NR3aC(O)OCH2-Cy1, —NR3aC(O)NR3b-Cy1, —NR3aC(O)NR3bCH2-Cy1, —NR3aC(O)CH2O-Cy1, —NR3aC(O)CH2-Cy1, —NR3aC(O)CH2CH2-Cy1, —C(O)NR3a-Cy1, —C(O)NR3aCH2-Cy1, or —C(O)NR3aCH2CH2-Cy wherein R3a and R3b are independently hydrogen atom or C1-6 alkyl group; and
Cy1 is a group of the following formula (11), (12), or (13):
wherein ring Q2 is optionally-substituted benzene ring, optionally-substituted pyridine ring, optionally-substituted pyrimidine ring, optionally-substituted pyridazine ring, or optionally-substituted pyrazine ring;
ring Q3 is optionally-substituted 5-membered heteroaryl ring;
n and m are independently 0, 1 or 2, provided that n and m are not simultaneously 0;
X is NR5 or O wherein R5 is hydrogen atom or C1-6 alkyl group which may be optionally substituted with the same or different 1 to 3 halogen atoms;
p is 1, 2, 3, 4 or 5; and
R4 is, independently when two or more exist, hydrogen atom, halogen atom, or C1-6 alkyl group which may be optionally substituted with the same or different 1 to 3 halogen atoms.
(a) halogen atom,
(b) C1-6 alkyl which may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(c) C1-6 alkoxy which may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(d) cyano,
(e) C6-10 aryl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl, and C1-6 alkoxy,
(f) 5- or 6-membered heteroaryl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl, and C1-6 alkoxy,
(g) C6-10 aryloxy which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl, and C1-6 alkoxy,
(h) hydroxy,
(i) amino which may be optionally substituted with the same or different 1 to 2 C1-6 alkyl groups,
(j) aminocarbonyl wherein the amino moiety thereof may be optionally substituted with the same or different 1 to 2 C1-6 alkyl groups,
(k) C1-6 alkoxy-carbonyl wherein the alkoxy moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(l) C1-6 alkyl-carbonyl wherein the alkyl moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(m) C1-6 alkylsulfonyl wherein the alkyl moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(n) C1-6 alkyl-carbonylamino wherein the alkyl moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(o) C1-6 alkylsulfonylamino wherein the alkyl moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(p) C1-6 alkoxy-carbonylamino wherein the alkoxy moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(q) alkyl-carbonyloxy wherein the alkyl moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(r) aminosulfonyl wherein the amino moiety thereof may be optionally substituted with the same or different 1 to 2 C1-6 alkyl groups, and
(s) C3-10 cycloalkyl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
W1 is C1-4 alkylene group which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy;
ring Q2 is benzene ring, pyridine ring, pyrimidine ring, pyridazine ring, or pyrazine ring wherein the benzene ring, pyridine ring, pyrimidine ring, pyridazine ring, and pyrazine ring may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom; C1-6 alkyl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of the same or different 1 to 3 halogen atoms, hydroxy and C1-6 alkoxy; C1-6 alkoxy which may be optionally substituted with the same or different 1 to 3 halogen atoms; hydroxy; and cyano;
ring Q3 is 5-membered heteroaryl ring which may be optionally substituted with halogen atom or C1-6 alkyl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of the same or different 1 to 3 halogen atoms, hydroxy and C1-6 alkoxy.
(a) halogen atom,
(b) C1-6 alkyl which may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy and C1-6 alkoxy,
(c) C1-6 alkoxy which may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy and C1-6 alkoxy,
(d) cyano,
(e) phenyl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl and C1-6 alkoxy,
(f) 5- or 6-membered heteroaryl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl and C1-6 alkoxy, and
(g) phenoxy which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl and C1-6 alkoxy,
(a) halogen atom,
(b) C1-6 alkyl which may be optionally substituted with the same or different 1 to 3 halogen atoms, and
(c) C1-6 alkoxy which may be optionally substituted with the same or different 1 to 3 halogen atoms.
or a pharmaceutically acceptable salt thereof, wherein ring Q1a is phenyl group, pyridyl group, or cyclohexyl group;
q is 1, 2, 3, 4 or 5;
R11 is, independently when two or more exist,
R1 and R2 are independently hydrogen atom, halogen atom, or C1-6 alkyl group which may be optionally substituted with the same or different 1 to 3 halogen atoms;
W1a is methylene group which may be optionally substituted with the same or different 1 to 2 halogen atoms or ethylene group which may be optionally substituted with the same or different 1 to 4 halogen atoms;
W2a-Cy2 is —NR3aC(O)-Cy2 or —C(O)NR3a-Cy2 wherein R3a is hydrogen atom or C1-6 alkyl group; and
Cy2 is a group of the following formula (21), (22), or (23):
wherein X1 is N or CR12;
X2 is N or CR13;
X3 is N or CR14;
X4 is N or CR15;
X5 is S, O or NH;
provided that X1, X2 and X3 are not simultaneously N;
R12, R13, R14 and R15 are independently
n and m are independently 0, 1 or 2, provided that n and m are not simultaneously 0;
p is 1, 2, 3, 4 or 5; and
R4 is, independently when two or more exist, hydrogen atom, halogen atom, or C1-6 alkyl group which may be optionally substituted with the same or different 1 to 3 halogen atoms.
or a pharmaceutically acceptable salt thereof, wherein is N or CR12;
X2 is N or CR13;
X3 is N or CR14;
provided that X1, X2 and X3 are not simultaneously N;
W2b is —NHC(O)— or —C(O)NH—;
R12, R13, R14, R21, R22, R23, R24, and R25 are independently
n and m are independently 0, 1 or 2, provided that n and m are not simultaneously 0;
p is 1, 2, 3, 4 or 5; and
R4 is, independently when two or more exist, hydrogen atom, halogen atom, or C1-6 alkyl group which may be optionally substituted with the same or different 1 to 3 halogen atoms.
N-(7-fluoro-1,2,3,4-tetrahydroisoquinolin-6-yl)-1-(3,4,5-trifluorobenzyl)-1H-imidazole-4-carboxamide (Example 1),
N-(5,6,7,8-tetrahydro-2,7-naphthyridin-3-yl)-1-(3,4,5-trifluorobenzyl)-1H-imidazole-4-carboxamide (Example 3),
N-(1,2,3,4-tetrahydroisoquinolin-6-yl)-1-(3,4,5-trifluorobenzyl)-1H-imidazole-4-carboxamide (Example 4),
8-fluoro-N-[1-(3,4,5-trifluorobenzyl)-1H-imidazol-4-yl]-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 5),
N-[1-(3,4,5-trifluorobenzyl)-1H-imidazol-4-yl]-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 6),
N-[1-(3,4,5-trifluorobenzyl)-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-2,7-naphthyridine-3-carboxamide (Example 8),
N-{1-[3-(trifluoromethyl)benzyl]-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-2,7-naphthyridine-3-carboxamide (Example 9),
N-{1-[3-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-5,6,7,8-tetrahydro-1,6-naphthyridine-2-carboxamide (Example 10),
N-[1-(3,4,5-trifluorobenzyl)-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-1,6-naphthyridine-2-carboxamide (Example 11),
N-[1-(3,4,5-trifluorobenzyl)-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 12),
N-{1-[3-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 13),
N-{1-[3-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 19),
1-(3,4-difluorobenzyl)-N-(5,6,7,8-tetrahydro-2,7-naphthyridin-3-yl)-1H-imidazole-4-carboxamide (Example 35),
N-[1-(3,5-difluorobenzyl)-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 47),
N-[1-(3,4-difluorobenzyl)-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 48),
N-{1-[3-(trifluoromethoxy)benzyl]-1H-imidazol-4-yl}-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 49),
N-[1-(3-phenoxybenzyl)-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-1, 7-naphthyridine-3-carboxamide (Example 50),
N-[1-(4-chloro-3-fluorobenzyl)-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 51),
N-[1-(3-chloro-5-fluorobenzyl)-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 52),
N-{1-[4-fluoro-3-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 53),
N-{1-[4-chloro-3-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 54),
N-{1-[4-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 64),
N-[1-(4-chlorobenzyl)-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 65),
N-{1-[3-chloro-5-(trifluoromethoxy)benzyl]-1H-imidazol-4-yl}-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 70),
N-[1-(3-phenoxybenzyl)-1H-imidazol-4-yl]-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 89),
N-[1-(4-chloro-3-fluorobenzyl)-1H-imidazol-4-yl]-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 90),
N-[1-(3-chloro-5-fluorobenzyl)-1H-imidazol-4-yl]-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 91),
N-{1-[4-fluoro-3-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 92),
N-(1-[4-chloro-3-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 93),
N-[1-(3-chloro-4-fluorobenzyl)-1H-imidazol-4-yl]-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 95),
N-{1-[4-methyl-3-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 97),
N-{1-[3-fluoro-5-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 99),
N-{1-[3-chloro-5-(trifluoromethoxy)benzyl]-1H-imidazol-4-yl}-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 100),
N-[1-(3,5-dichlorobenzyl)-1H-imidazol-4-yl]-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 101), and
N-[1-(3,4-dichlorobenzyl)-1H-imidazol-4-yl]-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 102).
N-(5,6,7,8-tetrahydro-2,7-naphthyridin-3-yl)-1-(3,4,5-trifluorobenzyl)-1H-imidazole-4-carboxamide (Example 3),
8-fluoro-N-[1-(3,4,5-trifluorobenzyl)-1H-imidazol-4-yl]-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 5),
N-[1-(3,4,5-trifluorobenzyl)-1H-imidazol-4-yl]-1,2,3,4-tetrahydroisoquinoline-6-carboxamide (Example 6),
N-{1-[3-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-5,6,7,8-tetrahydro-1,6-naphthyridine-2-carboxamide (Example 10),
N-[1-(3,4,5-trifluorobenzyl)-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-1,6-naphthyridine-2-carboxamide (Example 11),
N-[1-(3,4,5-trifluorobenzyl)-1H-imidazol-4-yl]-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 12), and
N-{1-[3-(trifluoromethyl)benzyl]-1H-imidazol-4-yl}-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxamide (Example 13).
The present compound has a potent inhibitory effect on the sphere-forming ability of cancer cells. In addition, the preferred present compound has high biological availability (bioavailability) after oral administration. Thus, the present compound is useful as an orally-available anti-cancer agent.
Hereinafter, the present invention is explained in detail. The number of carbon atoms in the definition of the “substituent” used herein may be expressed as, for example, “C1-6”. Specifically, the term “C1-6 alkyl” is used for the same meaning as alkyl group having 1 to 6 carbon atoms.
Specific examples of “halogen atom” used herein include fluorine atom, chlorine atom, bromine atom, and iodine atom.
The term “C1-6 alkyl group” used herein means a straight or branched, saturated hydrocarbon group having 1 to 6 carbon atoms. Preferred examples thereof include “C1-4 alkyl group”. Specific examples of the “C1-6 alkyl group” include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, neopentyl, 1-ethylpropyl, hexyl, isohexyl, 1,1-dimethylbutyl, 2,2-dimethylbutyl, 3,3-dimethylbutyl, and 2-ethylbutyl.
The term “C1-4 alkylene group” used herein means a straight or branched, divalent saturated hydrocarbon group having 1 to 4 carbon atoms, or a divalent saturated hydrocarbon group containing a cyclic structure having 3 to 4 carbon atoms.
Specific examples of the straight or branched “C1-4 alkylene group” include methylene, ethylene, trimethylene, tetramethylene, 1-methylmethylene, 1-ethylmethylene, 1-propylmethylene, 1-methylethylene, 2-methylethylene, and 1-ethylethylene. Preferred examples thereof include methylene and ethylene.
Specific examples of the “C1-4 alkylene group” containing a cyclic structure include the following groups:
The “C1-6 alkyl” moiety of the term “C1-6 alkoxy group” used herein is as defined in the above “C1-6 alkyl”. Preferred examples thereof include “C1-4 alkoxy group”. Specific examples of the “C1-6 alkoxy group” include methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, sec-butoxy, and tert-butoxy.
The term “C3-10 cycloalkyl group” used herein means a to 10-membered monocyclic or polycyclic, saturated or partially-unsaturated hydrocarbon group. The group is preferably “C3-7 cycloalkyl group”, and more preferably cyclohexyl group. Specific examples of the “C3-10 cycloalkyl group” include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclopentenyl, cyclohexenyl, decalinyl, adamantyl, and norbornyl.
The term “C6-10 aryl group” used herein means an aromatic hydrocarbon group having 6 to 10 carbon atoms. The group is preferably “C6 aryl group” (phenyl). Specific examples of the “C6-10 aryl group” include phenyl, 1-naphthyl, or 2-naphthyl.
Examples of the term “5- to 10-membered heteroaryl group” used herein include a 5- to 10-membered mono- or bi-cyclic aromatic group which contains the same or different one or more (e.g. 1 to 4) heteroatoms selected from the group consisting of nitrogen atom, sulfur atom, and oxygen atom. The bicyclic heteroaryl group also encompasses a fused ring group of a monocyclic heteroaryl group mentioned above with an aromatic group (such as benzene and pyridine) or a non-aromatic ring (such as cyclohexyl and piperidine). Specific examples of the “heteroaryl group” include the groups of the following formulae:
The bond across a ring in the above formulae means that a “group” is linked at any replaceable position in the ring. For example, when a group is the heteroaryl group of the following formula:
the group means 2-pyridyl group, 3-pyridyl group, or 4-pyridyl group.
Furthermore, when a “heteroaryl group” is a bicyclic group, for example, the group of the following formula:
the group may be 1-benzimidazolyl, 2-benzimidazolyl, or 4-, 5-, 6- or 7-benzimidazolyl.
In the groups of formulae (11), (12) and (13) defined in the above [1], the two atoms indicated by arrows, which are shared between ring Q2 or ring Q3 and another ring fused with the ring, are carbon.
The term “aminocarbonyl group” used herein means a formyl group wherein hydrogen atom therein is replaced with amino group.
The “C1-6 alkyl” moiety of the term “C1-6 alkyl-carbonylamino group” used herein is as defined in the above “C1-6 alkyl”. Preferred examples thereof include “C1-4 alkyl-carbonylamino group”, more preferably methylcarbonylamino group (acetamido group).
The “C6-10 aryl” moiety of the term “C6-10 aryloxy group” is as defined in the above “C6-10 aryl”. Preferred examples thereof include “C6 aryloxy group” (phenoxy group).
The “C1-6 alkoxy” moiety of the term “C1-6 alkoxy-carbonyl group” used herein is as defined in the above “C1-6 alkoxy”. Preferred examples thereof include “C1-4 alkoxy-carbonyl group”. Specific examples of the “C1-6 alkoxy-carbonyl group” include methoxycarbonyl, ethoxycarbonyl, and propoxycarbonyl.
The “C1-6 alkyl” moiety of the term “C1-6 alkyl-carbonyl group” used herein is as defined in the above “C1-6 alkyl”. Preferred examples thereof include “C1-4 alkyl-carbonyl group”. Specific examples of the “C1-6 alkyl-carbonyl group” include acetyl, ethylcarbonyl, and propylcarbonyl.
The “C1-6 alkyl” moiety of the term “C1-6 alkylsulfonyl group” used herein is as defined in the above “C1-6 alkyl”. Preferred examples thereof include “C1-4 alkylsulfonyl group”. Specific examples of the “C1-6 alkylsulfonyl group” include methylsulfonyl, ethylsulfonyl, and propylsulfonyl.
The “C1-6 alkyl” moiety of the term “C1-6 alkylsulfonylamino group” used herein is as defined in the above “C1-5 alkyl”. Preferred examples thereof include “C1-4 alkylsulfonylamino group”. Specific examples of the “C1-6 alkylsulfonylamino group” include methylsulfonylamino, ethylsulfonylamino, and propylsulfonylamino.
The “C1-6 alkoxy” moiety of the term “C1-6 alkoxy-carbonylamino group” used herein is as defined in the above “C1-6 alkoxy”. Preferred examples thereof include “C1-4 alkoxy-carbonylamino group”. Specific examples of the “C1-6 alkoxy-carbonylamino group” include methoxycarbonylamino, ethoxycarbonylamino, and propoxycarbonylamino.
The term “C1-6 alkyl-carbonyloxy group” used herein means an oxy group substituted with the above “C1-6 alkyl-carbonyl group”. Preferred examples thereof include “C1-4 alkyl-carbonyloxy group”. Specific examples of the “C1-6 alkyl-carbonyloxy group” include acetoxy, propionyloxy, and butyryloxy.
The term “aminosulfonyl group” used herein means a sulfo group wherein hydroxy group therein is substituted with amino group.
Examples of the substituent in the term “optionally-substituted C1-4 alkylene group” include hydroxy group, halogen atom, C3-7 cycloalkyl group, and C1-6 alkoxy group, preferably fluorine atom.
Examples of the substituent in the terms “optionally-substituted C5-10 aryl group”, “optionally-substituted C3-10 cycloalkyl group”, “optionally-substituted 5- to 10-membered heteroaryl group”, “optionally-substituted benzene ring”, “optionally-substituted pyridine ring”, “optionally-substituted pyrimidine ring”, “optionally-substituted pyridazine ring”, “optionally-substituted pyrazine ring”, “optionally-substituted 5-membered heteroaryl ring” include
(a) halogen atom,
(b) C1-6 alkyl which may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(c) C1-6 alkoxy which may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(d) cyano,
(e) C6-10 aryl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl, and C1-6 alkoxy, and
(f) 5- or 6-membered heteroaryl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl, and C1-6 alkoxy,
(g) C6-10 aryloxy which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl, and C1-6 alkoxy,
(h) hydroxy,
(i) amino which may be optionally substituted with the same or different 1 to 2 C1-6 alkyl groups,
(j) aminocarbonyl wherein the amino moiety thereof may be optionally substituted with the same or different 1 to 2 C1-6 alkyl groups,
(k) C1-6 alkoxy-carbonyl wherein the alkoxy moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(l) C1-6 alkyl-carbonyl wherein the alkyl moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(m) C1-6 alkylsulfonyl wherein the alkyl moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(n) C1-6 alkyl-carbonylamino wherein the alkyl moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(o) C1-6 alkylsulfonylamino wherein the alkyl moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(p) C1-6 alkoxy-carbonylamino wherein the alkoxy moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(q) C1-6 alkyl-carbonyloxy wherein the alkyl moiety thereof may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(r) aminosulfonyl wherein the amino moiety thereof may be optionally substituted with the same or different 1 to 2 C1-6 alkyl groups, and
(s) C3-10 cycloalkyl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy.
In the present compound of formula (1), W1, W2, R1, R2, R4, X, n, m, p, ring Q1, and Cy1 are preferably those shown below, but the technical scope of the present invention should not be limited to the following compounds.
W1 is preferably C1-4 alkylene group which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy. W1 is more preferably methylene group which may be optionally substituted with the same or different 1 to 2 halogen atoms or ethylene group which may be optionally substituted with the same or different 1 to 4 halogen atoms, furthermore preferably methylene group.
W2-Cy1 preferably includes —NR3aC(O)-Cy1 or C(O)NR3a-Cy1 wherein R3a is hydrogen atom or C1-6 alkyl group. W2-Cy1 is more preferably —NHC(O)—Cy1 or —C(O)NH-Cy1, furthermore preferably —NHC(O)-Cy1.
Preferably, R1 and R2 independently includes hydrogen atom, halogen atom, C1-4 alkyl group which may be optionally substituted with the same or different 1 to 3 halogen atoms. R1 and R2 are more preferably hydrogen atom, chlorine atom, or methyl group, furthermore preferably hydrogen atom.
Ring Q1 preferably includes
(a) halogen atom,
(b) C1-5 alkyl which may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(c) C1-6 alkoxy which may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(d) cyano,
(e) phenyl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl, and C1-6 alkoxy,
(f) 5- or 6-membered heteroaryl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl, and C1-6 alkoxy,
(g) phenoxy which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl, and C1-6 alkoxy,
(h) hydroxy,
(i) amino which may be optionally substituted with the same or different 1 to 2 alkyl groups, and
(j) aminocarbonyl wherein the amino moiety thereof may be optionally substituted with the same or different 1 to 2 C1-6 alkyl groups,
Ring Q1 preferably includes
(a) halogen atom,
(b) C1-6 alkyl which may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(c) C1-6 alkoxy which may be optionally substituted with the same or different 1 to 3 groups selected from the group consisting of halogen atom, hydroxy, and C1-6 alkoxy,
(d) cyano,
(e) phenyl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl, and C1-6 alkoxy, and
(f) 5- or 6-membered heteroaryl which may be optionally substituted with the same or different 1 to 4 groups selected from the group consisting of halogen atom, C1-6 alkyl, and C1-6 alkoxy, or
Ring Q1 furthermore preferably includes phenyl group which may be optionally substituted with the same or different 1 to 5 groups selected from the group consisting of:
(a) halogen atom,
(b) C1-6 alkyl which may be optionally substituted with the same or different 1 to 3 halogen atoms, and
(c) C1-6 alkoxy which may be optionally substituted with the same or different 1 to 3 halogen atoms.
Cy1 preferably includes the group of formula (11) in the above [1].
Preferred aspects of the group of formula (11) in the above [1] include the group of formula (21) in the above [9].
More preferably, it includes the following groups:
wherein R4, n, m, and p are as defined in the above [1]; and R, R13 and R14 are as defined in the above [9].
Furthermore preferably, it includes the above groups of formulae (21a), (21b), (21c) and (21d).
Preferred aspects of the group of formula (12) in the above [1] include the group of formula (22) in the above [9].
More preferably, it includes the following groups:
wherein R4, n, m, and p are as defined in the above [1]; and R15 is as defined in the above [9].
It furthermore preferably includes the above groups of formulae (22a) and (22b), most preferably the above group of formula (22a).
Preferred aspects of the group of formula (13) in the above [1] include the group of formula (23) in the above [9].
More preferably, it includes the following groups:
wherein R4, n, and p are as defined in the above [1]; and R12, R13, and R14 are as defined in the above [9].
Furthermore preferably, it includes the above group of formula (23a).
R4 preferably includes hydrogen atom, fluorine atom, or C1-4 alkyl. R4 is more preferably hydrogen atom.
p in the above [1] and q in the above [9] are independently selected from 1, 2, 3, 4, or 5. Preferably, p and q are independently 1, 2, or 3. When the number of the replaceable positions on the ring having the substituent R4 or R11 is less than 5, p and q are independently selected from the maximum replaceable number of R4 or R11. For example, when ring Q1 is pyridyl group, q is selected from 1, 2, 3, or 4.
X preferably includes NR5 wherein R5 is hydrogen atom or C1-6 alkyl group which may be optionally substituted with the same or different 1 to 3 halogen atoms, and more preferably it is NH.
With regard to n and m, preferably n is 1 and m is 1; or n is 2 and m is 0. More preferably, n is 1 and m is 1.
The present compound may be in the forms of a hydrate and/or a solvate. Thus, the present compound also encompasses hydrate and/or solvate such as ethanol solvate. Furthermore, the present compound encompasses all types of crystal forms of the present compound.
Specific examples of the pharmaceutically acceptable salt of the compound of formula (1) include an inorganic acid salt such as hydrochloride, hydrobromide, sulfate, phosphate, and nitrate; and an organic acid salt such as acetate, propionate, oxalate, succinate, lactate, malate, tartrate, citrate, maleate, fumarate, methanesulfonate, p-toluenesulfonate, benzenesulfonate, and ascorbate.
The compound of formula (1) may be in the form of a tautomer. Thus, the present compound also encompasses the tautomer of the compound of formula (1).
The compound of formula (1) may contain one or more asymmetric carbon atoms. Thus, the present compound encompasses not only racemic forms of the compound of formula (1) but also optically-active forms thereof. When the compound of formula (1) contains two or more asymmetric carbon atoms, the compound can result in various stereoisomerisms. Thus, the present compound also encompasses the stereoisomer of the compound and a mixture or isolate thereof.
Also, the compound of formula (1) encompasses the compound wherein one or more of 1H are replaced with 2H(D) (i.e. deuterated form).
Preparations
The present compounds can be prepared according to processes shown below and according to the processes in combination with known compounds and known synthesis processes.
As appropriate, each compound used as a starting compound may be used in the salt form. The shown processes are just examples to prepare the compounds, and may be optionally modified by those skilled in the organic synthesis field.
In each process shown below, any functional groups which need to be protected may be optionally protected and then deprotected after the reaction or reactions are completed to give the desired compound even though the use of protective groups is not specifically described.
The protective group used herein includes any conventional groups described in various literatures, for example, T. W. Greene and P. G. M. Wuts, “Protective Groups in Organic Synthesis”, 3rd Ed., John Wiley and Sons, inc., New York (1999). In more detail, specific examples of the protective groups for amino group include benzyloxycarbonyl, tert-butoxycarbonyl, acetyl, and benzyl, and specific examples of the protective groups for hydroxy group include trialkylsilyl, acetyl, and benzyl.
The protective groups can be introduced and cleaved according to commonly-used methods in synthetic organic chemistry (e.g. the method described in T. W. Greene and P. G. M. Nuts, “Protective Groups in Organic Synthesis”, 3rd Ed., John Wiley and Sons, inc., New York (1999)) and similar methods thereto.
One of the compounds of formula (1), the compound of formula (1-8) is prepared by linking each fragment in positions a, b and c, respectively:
wherein W1, R1, R2, R4, R5, n, m, p, ring Q1, and ring Q2 are as defined in the above [1].
The processes for forming each bond in positions a, b and c can be illustrated as follows, but the order of procedure for forming each bond may be optionally changed:
wherein W1, R1, R2, R4, R5, n, m, p, ring Q1, and ring Q2 are as defined in the above [1]; L is a leaving group (such as iodine atom, bromine atom, chlorine atom and substituted sulfonyl group (e.g. methanesulfonyl group and p-toluenesulfonyl group)); and R101 is benzyloxycarbonyl (Cbz) group, Boc group, benzyl group, 4-methoxybenzyl group, or 9-fluorenylmethyloxycarbonyl (Fmoc) group.
Compound (1-1) may be a commercially available product or be prepared according to known synthesis processes (e.g. New Version of Heterocyclic Compound (advanced level) edited by Kodansha Scientific Ltd.).
Compound (1-3) is prepared by the alkylation reaction of compound (1-1) with compound (1-2) in an inert solvent in the presence of a base.
Specific examples of the base include an organic base such as triethylamine, diisopropylethylamine, and pyridine; an inorganic base such as potassium carbonate, sodium carbonate, cesium carbonate, potassium hydrogen carbonate, sodium hydrogen carbonate, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, potassium phosphate, sodium dihydrogen phosphate, disodium hydrogen phosphate, sodium phosphate, potassium hydroxide, sodium hydroxide, and sodium hydride; and a metal alkoxide such as sodium methoxide and potassium tert-butoxide.
Specific examples of the inert solvent include a halogenated hydrocarbon such as chloroform and dichloromethane; an aromatic hydrocarbon such as toluene; an ether-type solvent such as diethyl ether, tetrahydrofuran (THF), and 1,4-dioxane; an aprotic polar solvent such as acetonitrile, acetone, methyl ethyl ketone, N,N-dimethylformamide, N-methyl-2-pyrrolidinone, and dimethylsulfoxide; a basic solvent such as pyridine; and a mixture thereof.
The reaction temperature is typically 0° C. to 150° C., preferably 20° C. to 100° C., but is not limited thereto. The reaction time is typically 30 minutes to 48 hours, preferably 30 minutes to 10 hours.
Compound (1-4) is prepared by reducing the nitro group in compound (1-3). For example, reactions such as reduction under an acidic condition with a metal such as zinc, iron and tin or a metal salt such as tin (II) chloride; reduction with a sulfide such as sodium dithionite (Na2S2O4); or catalytic hydrogenation with a metal catalyst such as palladium/carbon, Raney nickel, platinum oxide/carbon, and rhodium/carbon under hydrogen atmosphere are used.
In the reduction reaction with a metal or a metal salt, the amount of the metal or the metal salt to be used is typically about 1 mole to 100 moles, preferably about 10 moles to 30 moles per mole of compound (1-3). Also, the amount of the acid to be used is typically about 1 mole to 100 moles, preferably about 10 moles to 30 moles per mole of compound (1-3). The reduction reaction is typically carried out in a solvent which has no negative effect on the reaction (e.g. ethanol). The reaction temperature is typically 0° C. to 100° C., but is not limited thereto. The reaction time is typically 30 minutes to 8 hours.
In the catalytic hydrogenation reaction, the amount of the metal catalyst to be used for compound (1-3) is typically 0.1% by weight to 1000% by weight, preferably 1% by weight to 100% by weight. The reaction may be carried out in a solvent such as an alcohol such as methanol; an ether such as tetrahydrofuran; and an ester such as ethyl acetate. The hydrogen pressure is typically 1 atm to 100 atms, preferably 1 atm to 5 atms. The reaction temperature is typically 0° C. to 120° C., preferably 20° C. to 80° C., but is not limited thereto. The reaction time is typically 30 minutes to 72 hours, preferably 1 hour to 48 hours.
Also, the reaction may be carried out in the presence of an acid catalyst, as appropriate. For example, an organic acid such as formic acid, acetic acid and trifluoroacetic acid, and an inorganic acid such as sulfuric acid, hydrochloric acid and hydrobromic acid are used as the acid catalyst. The amount of the acid to be used is 0.1 mole or more per mole of compound (1-3).
Compound (1-6) is prepared by reacting compound (1-4) with compound (1-5) in an inert solvent in the presence of a condensation agent.
The reaction may be carried out in the presence of a base, as appropriate. The reaction temperature is typically about −20° C. to the boiling point of the used solvent, but is not limited thereto. The reaction time is typically 10 minutes to 48 hours, which may vary according to various conditions such as a reaction temperature, a condensation agent, a starting material, and a solvent to be used.
Specific examples of the condensation agent include dicyclohexylcarbodiimide (DCC), diisopropylcarbodiimide (DIPC), 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (WSC), benzotriazol-1-yl-tris(dimethylamino)phosphonium hexafluorophosphate (BOP), diphenylphosphonyl diamide (DPPA), N,N-carbonyldiimidazole (CDI), O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HBTU), and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU). As appropriate, the reaction may be carried out with the addition of an additive such as N-hydroxysuccinimide (HOSu), 1-hydroxybenzotriazole (HOBt), and 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HOOBt).
Specific examples of the base include an organic base such as triethylamine, diisopropylethylamine and pyridine; an inorganic base such as potassium carbonate, sodium carbonate, cesium carbonate, potassium hydrogen carbonate, sodium hydrogen carbonate, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, potassium phosphate, sodium dihydrogen phosphate, disodium hydrogen phosphate, sodium phosphate, potassium hydroxide, sodium hydroxide and sodium hydride; and a metal alkoxide such as sodium methoxide and potassium tert-butoxide.
Specific example of the inert solvent include a halogenated hydrocarbon such as chloroform and dichloromethane; an aromatic hydrocarbon such as toluene; an ether-type solvent such as diethyl ether, tetrahydrofuran (THF) and 1,4-dioxane; an aprotic polar solvent such as acetonitrile, acetone, methyl ethyl ketone, dimethylformamide, N-methyl-2-pyrrolidinone and dimethylsulfoxide; a basic solvent such as pyridine; and a mixture thereof.
Compound (1-6) is also prepared by reacting compound (1-4) with an acid halide or an acid anhydride derived from compound (1-5) in an inert solvent in the presence of a base.
Compound (1-7) is prepared using compound (1-6) as the starting material according to a similar process to the process described in literatures (such as Protective Groups in Organic Synthesis 3rd Edition (John Wiley & Sons, Inc.)).
Compound (1-8) is prepared by the reductive amination of compound (1-7) with an alkylketone or an alkylaldehyde in an appropriate inert solvent in the presence of a reducing agent.
The reaction may be carried out in the presence of a base, an acid or other additives, as appropriate. The reaction temperature is typically about −20° C. to the boiling point of the used solvent. The reaction time is typically 10 minutes to 48 hours, which may vary according to various conditions such as a reaction temperature, a reducing agent, a starting material, and a solvent to be used.
Specific examples of the reducing agent include sodium cyanoborohydride, sodium triacetoxyborohydride, and sodium borohydride.
Specific examples of the base include an organic base such as triethylamine, diisopropylethylamine and pyridine; and an inorganic base such as potassium carbonate, sodium carbonate, cesium carbonate, potassium hydrogen carbonate, sodium hydrogen carbonate, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, potassium phosphate, sodium dihydrogen phosphate, disodium hydrogen phosphate, sodium phosphate, potassium hydroxide, sodium hydroxide and sodium hydride.
Specific examples of the acid include an organic acid such as acetic acid, trifluoroacetic acid and methanesulfonic acid; and an inorganic acid such as hydrochloric acid and sulfuric acid.
Specific examples of the solvent include water; acetonitrile; a halogenated hydrocarbon such as chloroform and dichloromethane; an aromatic hydrocarbon such as benzene and toluene; an ether-type solvent such as 1,2-dimethoxyethane, tetrahydrofuran and 1,4-dioxane; an alcohol-type solvent such as methanol, ethanol and 2-propanol; an aprotic polar solvent such as dimethylformamide and N-methyl-2-pyrrolidinone; and a mixture thereof.
The compound of formula (2-5) is prepared according to, for example, the following process.
wherein R4, n, m, p, and ring Q2 are as defined in the above [1]; Xa is O or NR101; R101 is Cbz group, Boc group, benzyl group, 4-methoxybenzyl group or Fmoc group; R102 is C1-6 alkyl group; and L is a leaving group (such as iodine atom, bromine atom, chlorine atom and substituted sulfonyl group (e.g. methanesulfonyl group and p-toluenesulfonyl group)).
Compound (2-1) may be a commercially available product or be prepared according to known synthesis processes (e.g. WO 2009/056556, WO 2006/065215).
Compound (2-3) is prepared by introducing ester group to compound (2-1) under carbon monoxide atmosphere in the presence of palladium catalyst, phosphorus ligand, an alcohol of formula (2-2) in an inert solvent.
The pressure of carbon monoxide is selected according to various conditions such as a reaction temperature, a starting material, and a solvent to be used, as appropriate, and is typically 1 atm to 100 atms, preferably 1 atm to 5 atms. The reaction temperature is typically about −20° C. to the boiling point of the used solvent, preferably room temperature to the boiling point of the used solvent. The reaction may be carried out using a microwave reaction device. The reaction time is typically 10 minutes to 48 hours, which may vary according to various conditions such as a reagent, a reaction temperature, a starting material, and a solvent to be used.
Examples of the palladium catalyst include tetrakis(triphenylphosphine)palladium and di-tert-butylphosphinepalladium.
Examples of the inert solvent include N,N-dimethylformamide, N-methyl-2-pyrrolidinone, 1,4-dioxane and a mixture thereof.
In addition, an organic base such as N,N-diisopropylethylamine and triethylamine may be added thereto, as appropriate.
Compound (2-5) is prepared by hydrolyzing compound (2-3) according to a similar process to a known process (e.g. Protective Groups in Organic Synthesis 3rd Edition (John Wiley & Sons, Inc.), Comprehensive Organic Transformation, by R. C. Larock et al., VCH publisher Inc., 1989).
Compound (2-4) is prepared by the cyanation of compound (2-1) in an inert solvent in the presence of palladium catalyst, phosphorus ligand and a cyanating agent.
The reaction temperature is typically about −20° C. to the boiling point of the used solvent, preferably room temperature to the boiling point of the used solvent. The reaction may be carried out using a microwave reaction device. The reaction time is typically 10 minutes to 48 hours, which may vary according to various conditions such as a reaction temperature, a reagent, a starting material, and a solvent to be used.
Examples of the cyanating agent include sodium cyanide, potassium cyanide and zinc cyanide, preferably zinc cyanide.
Examples of the palladium catalyst include tetrakis(triphenylphosphine)palladium and di-tert-butylphosphinepalladium.
Examples of the inert solvent include N,N-dimethylformamide, N-methyl-2-pyrrolidinone, 1,4-dioxane and a mixture thereof.
Compound (2-5) is prepared by hydrolyzing the cyano group in compound (2-4) in an appropriate solvent in the presence of a base.
The reaction temperature is typically about −20° C. to the boiling point of the used solvent, preferably room temperature to the boiling point of the used solvent. The reaction time is typically 10 minutes to 48 hours, which may vary according to various conditions such as a reaction temperature, a starting material, and a solvent to be used.
Examples of the base include sodium hydroxide and potassium hydroxide.
Examples of the solvent to be used include methanol, ethanol, 2-propanol, acetone, tetrahydrofuran, 1,4-dioxane, water and a mixture thereof.
The compound of formula (3-6) is prepared by, for example, the following process.
wherein ring Q2 is as defined in the above [1]; A is boronic acid or boronate; R102 is C1-6 alkyl group, R103 is C1-6 alkyl group, benzyl group, allyl group, etc.; Ra and Rb are the same or different hydrogen atom or methyl group; and X is halogen atom.
Compound (3-3) is prepared by reacting compound (3-1) with compound (3-2) in an inert solvent in the presence of palladium catalyst and a base.
Specific examples of the palladium catalyst include tetrakis(triphenylphosphine)palladium (0), bis(dibenzylideneacetone)palladium (0), tris(dibenzylideneacetone)dipalladium (0), bis(tri-tert-butylphosphine)palladium (0), [1,1′-bis(diphenylphosphino)ferrocene]palladium (II) dichloride.
Examples of the base include an inorganic base such as potassium carbonate, sodium carbonate, cesium carbonate, potassium phosphate, potassium hydroxide and sodium hydroxide.
Examples of the inert solvent include toluene, 1,2-dimethoxyethane, 1,4-dioxane, DMF and a mixture thereof.
The reaction temperature is typically about 50° C. to 150° C., preferably 80° C. to 120° C., but is not limited thereto.
Also, the reaction may be carried out under microwave irradiation. The reaction time is typically 1 hour to 24 hours, preferably 2 hours to 12 hours.
Compound (3-4) is prepared by reacting compound (3-3) with osmium tetroxide or potassium osmate (IV) dihydrate in the presence of sodium periodate.
Examples of the solvent to be used include acetone, 1,4-dioxane, THF, tert-butanol, water and a mixture thereof.
The reaction temperature is typically about 0° C. to 100° C., preferably 25° C. to 50° C., but is not limited thereto. The reaction time is typically 1 hour to 72 hours, preferably 6 hours to 24 hours.
Also, compound (3-4) is prepared by treating compound (3-3) with oxygen currents including ozone and then reacting the treated compound with a reducing agent such as dimethyl sulfide at room temperature or −78° C. in a solvent such as dichloromethane, ethyl acetate and methanol. The reaction temperature is typically −78° C. to room temperature, but is not limited thereto. The reaction time is typically 1 hour to 72 hours, preferably 6 hours to 24 hours.
Compound (3-5) is prepared by reacting compound (3-4) with an organometallic reagent or a hydride reducing agent.
Specific examples of the organometallic reagent include methyllithium reagent and methyl Grignard reagent.
Specific examples of the hydride reducing agent include sodium borohydride and sodium cyanoborohydride.
The solvent used in the reaction with the organometallic reagent includes THF, diethyl ether and a mixture thereof, and the solvent used in the reaction with the hydride reducing agent includes methanol, ethanol, dichloromethane, toluene and a mixture thereof.
The reaction temperature is typically −78° C. to 50° C., preferably 0° C. to 25° C., but is not limited thereto. The reaction time is typically 5 minutes to 12 hours, preferably 30 minutes to 6 hours.
Compound (3-6) is prepared by reacting compound (3-5) with aqueous alkali solution.
Examples of the aqueous alkali solution include ageous sodium hydroxide solution, aqueous potassium hydroxide solution and aqueous lithium hydroxide solution, and the concentraton thereof is typically 1 to 10 mol/L, preferably 1 to 5 mol/L.
Examples of the solvent to be used include methanol, ethanol, 2-propanol, THF, 1,4-dioxane and a mixture threof.
The reaction temperature is typically 0° C. to 100° C., preferably 0° C. to 50° C., but is not limited thereto. The reaction time is typically 10 minutes to 24 hours, preferably 30 minutes to 12 hours.
The compound of formula (4-1) may be a commercially available product or be prepared according to known synthesis processes (e.g. J. Med. Chem., 2004, 5167-5182, Bioorg. Med. Chem., 2006, 1309-1330.).
One of the compounds of formula (1), the compound of formula (5-5) is prepared according to, for example, the following process.
wherein W1I, R1, R2, R4, n, m, p, ring Q2, and ring Q2 are as defined in the above [1]; R101 is Cbz group, Boc group, benzyl group, 4-methoxybenzyl group or Fmoc group; and R102 is C1-6 alkyl group.
The compound of formula (5-1) may be a commercially available product or be prepared according to known synthesis processes (e.g. WO 2014/125444).
Compound (5-2) is prepared by hydrolyzing compound (5-1) according to a similar process to a known process (e.g. Protective Groups in Organic Synthesis 3rd Edition (John Wiley & Sons, Inc.), Comprehensive Organic Transformation, by R. C. Larock et al., VCH publisher Inc., 1989).
Compound (5-4) is prepared from compounds (5-2) and (5-3) according to the process of Step 1-3.
Compound (5-5) is prepared using compound (5-4) as a starting material according to a simialr process to the process described in literatures (such as Protective Groups in Organic Synthesis 3rd Edition (John Wiley & Sons, Inc.)).
The compound of formula (1-6) is prpared by, for example, the following process.
wherein W1, R1, R2, R4, n, m, p, ring Q1, and ring Q2 are as defined in the above [1]; L is a leaving group (such as iodine atom, bromine atom, chlorine atom and substituted sulfonyloxy group (e.g. methanesulfonyloxy group and p-toluenesulfonyloxy group)); and R101 and R104 are benzyloxycarbonyl (Cbz) group, Boc group, benzyl group, 4-methoxybenzyl group, 2-(trimethylsilyl)ethoxymethyl group or 9-fluorenylmethyloxycarbonyl (Fmoc) group.
Compound (6-1) is prepared by introducing a protective group to N atom of the imidazole group in compound (1-1) in an inert solvent. Examples of the protective group include 2-(trimethylsilyl)ethoxymethyl, benzyloxycarbonyl, tert-butoxycarbonyl, acetyl and benzyl.
For example, when 2-(trimethylsilyl)ethoxymethyl group is introduced, compound (6-1) is prepared by reacting compound (1-1) with 2-(trimethylsilyl)ethoxymethyl chloride in an inert solvent in the presence of a base.
Examples of the base include potassium carbonate, sodium carbonate, cesium carbonate, potassium-tert-butoxide, sodium hydroxide, sodium bis(trimethylsilyl)amide, lithium bis(trimethylsilyl)amide, potassium bis(trimethylsilyl)amide and lithium diisopropylamide. Examples of the inert solvent include DMF, THF, acetonitrile and a mixture thereof.
The reaction temperature is typically 0° C. to 150° C., preferably 0° C. to 100° C., but is not limited thereto. The reaction time is typically 10 minutes to 24 hours, preferably 20 minutes to 6 hours.
Compound (6-2) is prepared from compound (6-1) according to the process of Step 1-2.
Compound (6-3) is prepared from compounds (6-2) and (1-5) according to the process of Step 1-3.
Compound (6-4) is prepared by cleaving the protective group for nitrogen atom of the imidazole group in compound (6-3) in an inert solvent.
For example, when 2-(trimethylsilyl)ethoxymethyl group is cleaved, compound (6-4) is prepared by reacting compound (6-3) with an acid or a fluorinating reagent in an inert solvent.
Examples of the acid include TFA, formic acid, hydrochloric acid, sulfuric acid, p-toluenesulfonic acid, methanesulfonic acid and (±) 10-camphorsulfonic acid.
Examples of the fluorinating reagent include tetrabutylammonium fluoride.
Examples of the solvent to be used include dichloromethane, 1,2-dichloroethane, 1,4-dioxane, THF, toluene, ethyl acetate, methanol, ethanol, 2-propanol and a mixture thereof.
The reaction temperature is typically 0° C. to 150° C., preferably 0° C. to 50° C., but is not limited thereto. The reaction time is typically 5 minutes to 24 hours, preferably 1 hour to 9 hours.
In Step 6-4, when R101 is cleaved simultaneously with cleaving the protective group for nitrogen atom of the imidazole group, compound (6-4) is prepared by reintroducing a protecting group to R101.
Compound (1-6) is prepared from compounds (6-4) and (1-2) according to the process of Step 1-1.
One of the compounds of formula (1-5), the compound of formula (7-4) is prepared according to, for example, the following process:
wherein R4, p, and ring Q2 are as defined in the above [1]; R101 is Cbz group, Boc group, benzyl group, 4-methoxybenzyl group, or Fmoc group; and R102 is C1-6 alkyl group.
Compound (7-1) may be a commercially available product or be prepared according to Preparation 8.
Compound (7-2) is prepared by reacting compound (7-1) with a hydride reducing agent in an inert solvent.
Specific examples of the hydride reducing agent include sodium borohydride, sodium cyanoborohydride, borane and hydride aluminium hydride.
Examples of the solvent to be used in the reaction with the hydride reducing agent include methanol, ethanol, dichloromehane, toluene, tetrahydrofuran and a mixture thereof.
The reaction temperature is typically −78° C. to 100° C., preferably 0° C. to 50° C., but is not limited thereto. The reaction time is typically 5 minutes to 12 hours, preferably 30 minutes to 6 hours.
Compound (7-3) is prepared by reducing olefin in compound (7-2) with a reagent for introducing a protective group. For example, reactions such as catalytic hydrogenation reaction with a metal catalyst such as palladium/carbon, Raney nickel, platinum oxide/carbon and rhodium/carbon under hydrogen atmosphere in the presence of Boc2O are used.
In the catalytic hydrogenation reaction, the amount of the metal catalyst to be used for compound (7-2) is typically 0.1% by weight to 1000% by weight, preferably 1% by weight to 100% by weight. The reaction may be carried out in a solvent such as an alcohol such as methanol; an ether such as tetrahydrofuran; and an ester such as ethyl acetate. The hydrogen pressure is typically atm to 100 atms, preferably 1 atm to 5 atms. The reaction temperature is typically 0° C. to 120° C., preferably 20° C. to 80° C., but is not limited thereto. The reaction time is typically 30 minutes to 72 hours, preferably 1 hour to 48 hours.
When R101 is benzyl group, 4-methoxybenzyl group, etc., compound (7-3) can be directly prepared through a pyridinium salt intermediate of compound (7-1). For example, compound (7-3) is prepared by reducing the pyridinium salt of compound (7-1) synthesized by reacting compound (7-1) with a reagent such as benzyl bromide. Reduction reactions such as reduction with a hydride reducing agent and catalytic hydrogenation with a metal catalyst such as palladium/carbon, Raney nickel, platinum oxide/carbon, and rhodium/carbon under hydrogen atmosphere are used.
Compound (7-4) is prepared by hydrolyzing compound (7-3) according to a similar process to a known process (e.g. Protective Groups in Organic Synthesis 3rd Edition (John Wiley & Sons, Inc.), Comprehensive Organic Transformation, by R. C. Larock et al., VCH publisher Inc., 1989).
One of the compounds of formula (7-1), the compound of formula (8-3) is prepared according to, for example, the following process:
wherein R4 and p are as defined in the above [1]; and R102 and R103 are C1-6 alkyl group.
Compound (8-3) is prepared by reacting compound (8-1) with compound (8-2) under an acidic condition in an inert solvent.
Examples of the acid used include trifluoroacetic acid, hydrochloric acid and sulfuric acid.
The reaction temperature is typically 0° C. to 150° C., preferably 0° C. to 100° C., but is not limited thereto. The reaction time is typically 5 minutes to 72 hours, preferably 30 minutes to 12 hours.
Examples of the inert solvent include dichloromethan, 1,2-dichloroethane, chloroform, THF, toluene, ethyl acetate and a mixture thereof.
The intermediates and desired compounds in the above preparations may be isolated and purified by a conventional purification method in organic synthetic chemistry such as neutralization, filtration, extraction, washing, drying, concentration, recrystallization, and each type of chromatography. The intermediates may be also used in the next reaction without any specific purification.
An optically-active product of the present compound can be prepared from an optically-active starting material or intermediate, or by the optical resolution of the racemate of a final product. The optical resolution method includes a physical separation method with optically-active column, and a chemical separation method such as a fractional crystallization method. A diastereomer of the present compound can be prepared by, for example, a fractional crystallization method.
The pharmaceutically acceptable salt of the compound of formula (1) can be prepared by, for example, mixing the compound of formula (1) with a pharmaceutically acceptable acid in a solvent such as water, methanol, ethanol, and acetone.
The present compound is used as, for example, an anti-tumor agent (anti-cancer agent). The applicable cancer type includes hematopoietic tumor and solid cancer, but is not limited thereto. Specific examples of the hematopoietic tumor include acute leukemia, chronic lymphatic leukemia, chronic myelocytic leukemia, polycythemia vera, malignant lymphoma, and myeloma, and specific examples of the solid cancer include brain tumor, head and neck cancer, esophageal cancer, thyroid cancer, small-cell lung cancer, non-small cell lung cancer, breast cancer, stomach cancer, gallbladder or bile duct cancer, liver cancer, pancreatic cancer, colon cancer, rectal cancer, ovarian cancer, chorioepithelioma, endometrial cancer, cervical cancer, urothelial cancer, renal cell cancer, prostate cancer, testicular tumor, Wilms' tumor, malignant melanoma, neuroblastoma, osteosarcoma, Ewing's sarcoma, and soft tissue sarcoma.
The anti-tumor agent is used for the prophylaxis and/or treatment of a cancer, and is expected to produce the reduction or disappearance of carcinoma or inhibit the growth of carcinoma down to a certain level. The “prophylaxis” used herein means the administration of the active ingredient of the present invention to a healthy subject who does not develop a disease. For example, the prophylaxis is intended to prevent the development of a disease. The “treatment” used herein means the administration of the active ingredient of the present invention to a person diagnosed with the development of a disease by a doctor (i.e. a patient). For example, the treatment is intended to alleviate a disease or symptom thereof, inhibit the growth of carcinoma, or improve the condition of a patient to the previous condition before a disease is developed. Also, even if an anti-tumor agent is administered for the purpose of preventing the worsening of a disease or symptom thereof or the growth of carcinoma, the administration is referred to as “treatment” when the subject to be administered is a patient.
The present compound has any remarkable effects for inhibiting self-renewal ability of CSCs, and thus is expected to be useful as a novel anti-tumor agent for inhibiting the persistent proliferation, metastasis, and recurrence of malignant tumors derived from CSCs.
The present compound may be formulated into a suitable dosage form and administered orally or parenterally. Examples of the dosage form include a tablet, a capsule, a powder, a granule, a solution, a suspension, an injection, a patch, and a poultice, but are not limited thereto. The preparation is formulated using pharmaceutically acceptable additive(s) according to a known method.
As appropriate, an additive such as an excipient, a disintegrant, a binder, a fluidizer, a lubricant, a coating agent, a solubilizer, a solubilizing agent, a thickening agent, a dispersant, a stabilizing agent, a sweetening agent, and a flavor may be used. Specific examples thereof include lactose, mannitol, crystalline cellulose, low substituted hydroxypropylcellulose, corn starch, partly pregelatinized starch, carmellose calcium, croscarmellose sodium, hydroxypropylcellulose, hydroxypropylmethylcellulose, polyvinylalcohol, magnesium stearate, sodium stearyl fumarate, polyethylene glycol, propylene glycol, titanium oxide, and talc.
The present compound may be used in combination with another drug(s) to enhance the therapeutic effect thereof and/or reduce side effects thereof. Specifically, the present compound can be used in combination with a drug such as a hormone therapeutic drug, a chemotherapeutic drug, an immunotherapeutic drug or a cell growth factor and a drug for inhibiting a receptor effect thereof. Hereinafter, a drug which can be used in combination with the present compound is referred to as “combined medicine”.
Examples of the combined medicine include an anticancer alkylating agent, an anticancer antimetabolite, an anticancer antibiotic, a plant-based anti-cancer agent, an anticancer platinum coordination compound, an anticancer camptothecin derivative, an anticancer tyrosine kinase inhibitor, a serine-threonine kinase, a phospholipid kinase, a monoclonal antibody, an interferon, a biological response modifier, a hormone preparation, an immune checkpoint inhibitor, an epigenetics-related molecule inhibitor, a post-translational protein modification inhibitor, and an anti-cancer agent other than the foregoings.
The administration timing of the present compound and a combined medicine is not necessarily limited, and they may be administered simultaneously or administered with time-interval to a subject. In addition, the present compound and a combined medicine may be used in the form of a combination drug. The dosage of the combined medicine may be optionally determined based on the dosage in the clinical use. Also, the mixing ratio of the present compound and a combined medicine may be optionally determined depending on the subject to be administered, the administration route, the disease to be treated, the symptom, and a combination thereof. For example, when the subject is human, the combined medicine may be used in an amount of 0.01 to 100 parts by weight relative to 1 part by weight of the present compound. In addition, a drug (a combined medicine) such as an antiemetic, a sleep inducing agent, and an anticonvulsant may be used in combination with the present compound to inhibit side effects thereof.
The dosage can vary according to each compound and various conditions such as patient's disease, age, body weight, sex, symptom, and administration route. Typically, the present compound is administered to an adult (body weight: 50 kg) at a dose of 0.1 to 1000 mg/day, preferably at a dose of 0.1 to 300 mg/day, which may be administered once a day or 2 or 3 times a day. In addition, the present compound may be administered once in several days to several weeks.
Hereinafter, the invention is illustrated in more detail with Reference Examples, Examples, and Test Examples, but the invention should not be limited thereto. The compound names as shown in the following Reference Examples and Examples do not necessarily follow the IUPAC nomenclature system.
The following abbreviations may be used herein.
THF: tetrahydrofuran
TFA: trifluoroacetic acid
(Boc)2O: di-tert-butyl dicarbonate
DMF: N,N-dimethylformamide
DIEA: N,N-diisopropylethylamine
EDCI: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide
EDCI.HCl: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
HOBt: 1-hydroxybenzotriazole
HOBt.H2O: 1-hydroxybenzotriazole monohydrate
Me: methyl
Et: ethyl
Ac: acetyl
Boc: tert-butoxycarbonyl
SEM: 2-(trimethylsilyl)ethoxymethyl
DMAP: N,N-dimethyl-4-aminopyridine
Rt: retention time
LC/MS analysis condition in the compound identification is as follows.
LC/MS measurement:
Detection device: ACQUITY® SQ deteceter (Waters)
HPLC: ACQUITY UPLC® system
Column: Waters ACQUITY UPLC® BEH C18 (1.7 μm, 2.1 mm×30 mm)
Solvent: A solution: 0.06% formic acid/H2O, B solution: 0.06% formic acid/MeCN
Gradient condition: 0.0-1.3 min Linear gradient from B 2% to 96%
Flow rate: 0.8 mL/min
UV: 220 nm and 254 nm
The compounds of Examples 38 to 41 were identified under the following LC/MS analysis condition.
LC/MS measurement:
Detection device: detector Perkin-Elmer Sciex API 150EX Mass spectrometer (40 eV)
HPLC: Shimadzu LC 10ATVP
Column: Shiseido CAPCELL PAK C18 ACR (S-5 μm, 4.6 mm×50 mm)
Solvent: A solution: 0.035% TFA/MeCN, B solution: 0.05% TFA/H2O
Gradient condition: 0.0-0.5 min A 10%, 0.5-4.8 min Linear gradient from A 10% to 99%, 4.8-5.0 min A 99%
Flow rate: 3.5 mL/min
UV: 220 nm and 254 nm
To a solution of methyl 4-imidazole-carboxylate (14.0 g) in acetonitrile (200 mL) were added potassium carbonate (19.9 g) and potassium iodide (0.092 g), and then 3,4,5-trifluorobenzyl bromide (14.6 mL) was added dropwise thereto at room temperature. The mixture was stirred at 70° C. for 6 hours and then cooled to room temperature, and to the reaction mixture was added water, and then the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, filtered, and then concentrated in vacuo. The resulting crude product was washed with hexane/ethyl acetate (1/2, 60 mL) to give the title compound (14.0 g).
LC-MS ([M+H]+/Rt (min)): 271.4/0.725
To a solution of the compound of Reference Example 1-1 (4.75 g) in methanol/THF (50 mL/50 mL) was added 2 mol/L aqueous sodium hydroxide solution (13.2 mL), and the mixture was stirred at 50° C. for 5 hours. The reaction mixture was concentrated in vacuo, and the residue was dissolved in water, and then aqueous hydrochloric acid solution was added thereto to adjust pH to 5. The resulting precipitate was collected on a filter, washed with water and hexane, and then dried at 50° C. in vacuo to give the title compound (4.52 g).
LC-MS ([M+H]+/Rt (min)): 257.1/0.513
According to the processes of Reference Example 1-1 and Reference Example 1-2, the title compound was prepared from 3,4-difluorobenzyl bromide.
LC-MS ([M+H]+/Rt (min)): 239.1/0.460
To a solution of the compound of Reference Example 1-2 (897 mg) in DMF (15 mL) were added tert-butyl 6-amino-7-fluoro-3,4-dihydroisoquinoline-2(1H)-carboxylate (932 mg), EDCI.HCl (805 mg), HOBt (567 mg) and N,N-diisopropylethylamine (1.22 mL), and the mixture was stirred at 80° C. for 7 hours. To the reaction mixture was added water and then aqueous sodium hydroxide, and the mixture was extracted with chloroform. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and then concentrated in vacuo. The residue was purified by silica gel column chromatography (chloroform/methanol) to give the title compound (1.50 g).
LC-MS ([M+H]+/Rt (min)): 505.3/1.137
According to the process of Reference Example 3, the compounds of Reference Examples 4 to 6 were prepared from the corresponding starting compounds.
To a solution of tert-butyl 6-hydroxy-1,2,3,4-tetrahydro-2, 7-naphthyridine-2-carboxylate (1.73 g) in pyridine (20 mL) was added trifluoromethanesulfonic anhydride (1.28 mL) with ice-cooling, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated in vacuo, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (1.72 g). LC-MS ([M+H]+/Rt (min)): 383.2/1.112
To acetic acid (15 mL) was added sodium borohydride (340 mg) at room temperature. To the reaction solution was added 6-bromo-5-fluoroisoquinoline (1.0 g), and the mixture was stirred at room temperature for 15 hours. To the reaction solution was added sodium borohydride (345 mg) at room temperature for 1 hour. The reaction mixture was concentrated in vacuo, and the residue was dissolved in THF (20 mL). Di-tert-butyl dicarbonate (2.04 g) and triethylamine (3.1 mL) were added thereto, and the mixture was stirred at room temperature for 2 hours. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, filtered, and then concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (1.17 g).
LC-MS ([M+H]+/Rt (min)): 330.2/1.213
According to the process of Reference Example 8, the compounds of Reference Examples 9 to 10 were prepared from the corresponding starting compounds.
4-Nitro-1H-imidazole (35.8 g), 3-trifluoromethylbenzyl bromide (75.7 g), potassium iodide (0.131 g), potassium carbonate (48.1 g) and acetonitrile (270 mL) were mixed, and the mixture was stirred at 80° C. for 5 hours. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and then concentrated in vacuo. To the resulting solid was added diisopropyl ether (300 mL), and the mixture was stirred at room temperature for 1 hour. The resulting precipitate was collected on a filter, washed with diisopropyl ether, and then dried at 50° C. in vacuo to give the title compound (69.0 g).
LC-MS ([M+H]+/Rt (min)): 272.1/0.835
To a solution of the compound of Reference Example 11-1 (34.0 g) in ethyl acetate (330 mL) was added rhodium-activated carbon (5%, 17.0 g), and the mixture was stirred under hydrogen atmosphere at room temperature for 14 hours.
The reaction mixture was filtered through Celite®, washed with ethyl acetate (50 mL×4), and then to the filtrate was added hydrogen chloride (4 mol/L in ethyl acetate, 38.0 mL). The filtrate was concentrated in vacuo, and then to the resulting crude product were added ethyl acetate (200 mL) and hexane (200 mL), and the mixture was stirred at room temperature for 10 minutes. The resulting precipitate was collected on a filter and washed with hexane/ethyl acetate (1/1, 20 mL×3), and then the resulting solid was dried at 40° C. in vacuo to give the title compound (31.4 g).
LC-MS ([M+H]+/Rt (min)): 242.1/0.548
According to the processes of Reference Examples 11-1 and 11-2, the title compound was prepared from 3,4,5-trifluorobenzyl bromide.
LC-MS ([M+H]+/Rt (min)): 228.1/0.473
To a solution of the compound of Reference Example 9 (124 mg) in DMF (1 mL) were added tetrakis(triphenylphosphine)palladium (45 mg) and zinc cyanide (57 mg), and the mixture was stirred at 120° C. for 8 hours. The reaction mixture was concentrated in vacuo, and then the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (48 mg).
LC-MS ([M+H]+/Rt (min)): 277.2/1.048
To a solution of the compound of Reference Example 13-1 (2.13 g) in 2-propanol (40 mL) were added water (10 mL) and sodium hydroxide (5 g), and the mixture was stirred at 110° C. for 11 hours. The reaction mixture was concentrated in vacuo, and the residue was extracted with saturated aqueous sodium bicarbonate solution. The aqueous layer was acidified with sodium hydrogen sulfate and extracted with chloroform. The resulting organic layer was dried over sodium sulfate and concentrated in vacuo to give the title compound (2.54 g).
LC-MS ([M+H]+/Rt (min)): 296.2/0.907
According to the processes of Reference Example 13-1 and 13-2-1, the compounds of Reference Example 13-2-2 to 13-2-4 were prepared from the corresponding starting compounds.
According to the process of Reference Example 3, the title compound was prepared from the compounds of Reference Example 13-2-1 and Reference Example 12.
LC-MS ([M+H]+/Rt (min)): 505.3/1.084
According to the process of Reference Example 3, the compounds of Reference Examples 14 to 31 were prepared from the corresponding starting compounds.
To a solution of methyl 5-amino-6-chloro-nicotinate (325 mg) in THF (10 mL) were added di-tert-butyl dicarbonate (760 mg) and DMAP (11 mg), and the mixture was stirred at room temperature for 15.5 hours. Additionally, di-tert-butyl dicarbonate (38 mg) was added thereto, and the mixture was stirred at 60° C. for 45 minutes. The mixture was cooled to room temperature, and the solvent therein was removed. To the residue were added methanol (5 mL) and potassium carbonate (481 mg), and the mixture was stirred at room temperature for 2.5 hours. Saturated aqueous ammonium chloride solution was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and then concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (321 mg).
LC-MS ([M+H]+/Rt (min)): 287.1/0.985
To a solution of the compound of Reference Example 32-1 (321 mg) in a mixture of 1,2-dimethoxyethane (9 mL)/water (0.9 mL) were added pinacol vinylboronate (0.575 mL), tetrakis(triphenylphosphine)palladium (129 mg) and potassium carbonate (465 mg), and the mixture was stirred under microwave irradiation at 120° C. for 1 hour. The mixture was cooled to room temperature, and to the reaction mixture was added water, and then the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, filtered, and then concentrated. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (207 mg).
LC-MS ([M+H]+/Rt (min)): 279.5/0.885
To a solution of the compound of Reference Example 32-2 (207 mg) in a mixture of acetone (8 mL)/water (4 mL) were added sodium periodate (659 mg) and osmium tetraoxide (2.5 wt % in tert-butanol, 0.71 mL), and the mixture was stirred at room temperature for 3 hours. To the reaction mixture were added saturated aqueous sodium thiosulfate solution and water, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, filtered, and then concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (110 mg).
LC-MS ([M+H]+/Rt (min)): 281.2/1.037
To a solution of the compound of Reference Example 32-3 (110 mg) in methanol was added sodium borohydride, and the mixture was stirred at room temperature for 1 hour. To the reaction mixture were added saturated aqueous ammonium chloride solution and water, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, filtered, and then concentrated in vacuo to give the title compound (111 mg).
LC-MS ([M+H]+/Rt (min)): 282.8/0.761
To a solution of the compound of Reference Example 32-4 (111 mg) in THF (2 mL)/methanol (4 mL) was added 2 mol/L aqueous sodium hydroxide solution (0.39 mL), and the mixture was stirred at room temperature for 16 hours. To the reaction mixture was added 2 mol/L hydrochloric acid (0.25 mL) to adjust pH to 7. The reaction mixture was concentrated in vacuo to give the title compound (76 mg).
LC-MS ([M+H]+/Rt (min)): 195.1/0.325
According to the process of Reference Example 3, the compound of Reference Example 33 was prepared from the corresponding starting compound.
According to the process of Reference Example 11-1, the compound of Reference Example 34 was prepared from the corresponding starting compound.
According to the process of Reference Example 11-2, the compound of Reference Example 35 was prepared from the compound of Reference Example 34.
According to the process of Reference Example 3, the compounds of Reference Examples 36 to 38 were prepared from the compound of Reference Example 35 and the corresponding starting compounds.
A solution of (3-aminopyridin-4-yl)-methanol (10.4 g) and manganese dioxide (50.3 g) in chloroform (100 mL) was stirred at room temperature for 18 hours. The reaction solution was filtered through Celite and concentrated to give the title compound (10.1 g).
LC-MS ([M+H]+/Rt (min)): 123.0/0.218
To a solution of the compound of Reference Example 39-1 (10.1 g) and ethyl 3-ethoxyacrylate (13.8 mL) in chloroform (100 mL) was added TFA (63.9 mL) with ice-cooling, and the mixture was stirred for 1 hour with heating under reflux. The reaction solution was concentrated, and the residue was dissolved in ethyl acetate, washed with saturated aqueous sodium bicarbonate solution and brine, dried over anhydrous sodium sulfate, filtered, and then concentrated in vacuo. The resulting crude product was dissolved in ethyl acetate (350 mL), and then 4 mol/L hydrochloric acid-ethyl acetate solution (42 mL) was added thereto, and the mixture was stirred for 1 hour. The resulting solid was filtered to give the title compound (16.8 g).
LC-MS ([M+H]+/Rt (min)): 203.1/0.619
Ethyl 7,8-dihydro-1,7-naphthyridine-3-carboxylate
To a solution of the compound of Reference Example 39-2 (3.13 g) in methanol (60 mL) was added sodium borohydride (1.49 g) with ice-cooling, and the mixture was stirred at room temperature for 30 minutes. Additionally, to the reaction solution was added sodium borohydride (0.8 g) with ice-cooling, and the mixture was stirred for 30 minutes. The reaction solution was concentrated, and then the residue was dissolved in ethyl acetate, washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give the title compound (2.68 g).
LC-MS ([M+H]+/Rt (min)): 205.1/0.420
A solution of the compound of Reference Example 39-3 (2.68 g), Boc2O (12.6 g) and palladium/carbon (1.6 g) in THF (100 mL) was stirred under hydrogen atmosphere at room temperature for 18 hours. The reaction solution was filtered through Celite® and concentrated. The resulting residue was purified by silica gel column chromatography to give the title compound (1.51 g).
LC-MS ([M+H]+/Rt (min)): 307.47/0.967
To a solution of the compound of Reference Example 39-4 (1.51 g) in THF (20 mL) were added water (5 mL) and 5 mol/L aqueous sodium hydroxide solution (1.5 mL) with ice-cooling, and the mixture was stirred at room temperature for 7 hours. The reaction solution was washed with diethyl ether, and then the aqueous phase was concentrated to give the title compound (1.51 g).
LC-MS ([M-H]+/Rt (min)): 279.2/0.707
A solution of 4-nitroimidazole in DMF (50 mL) was added dropwise to a solution of sodium hydride (10.3 g) in DMF (50 mL) with ice-cooling, and the mixture was stirred with ice-cooling for 30 minutes. 2-(Trimethylsilyl)ethoxymethyl chloride (17.5 mL) was added dropwise thereto with ice-cooling, and the mixture was stirred at room temperature for 1 hour. To the reaction solution were added methanol (30 mL) and ice, and the aqueous layer was extracted with hexane/ethyl acetate=1/1. The organic phase was dried over anhydrous magnesium sulfate, filtered, and then concentrated in vacuo. The resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (19.4 g).
LC-MS ([M+H]+/Rt (min)): 244.1/0.929
A solution of the compound of Reference Example 40-1 (3.01 g) and palladium/carbon (1.57 g) in ethyl acetate (30 mL) was stirred under hydrogen atmosphere at room temperature for 6 hours. The reaction solution was filtered through Celite®. To the resulting filtrate were added WSC (2.48 g), 2-(tert-butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid (2.29 g) and DIEA (4.33 mL), and the mixture was stirred at room temperature for 18 hours. The reaction solution was washed with saturated aqueous sodium bicarbonate solution and brine, dried over sodium hydrogen sulfate, filtered, and then concentrated. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (2.95 g).
LC-MS ([M+H]+/Rt (min)): 473.4/1.106
A solution of the compound of Reference Example 40-2 (1.08 g) in 4 mol/L dioxane hydrochloride (50 mL) was stirred for 8 hours with heating under reflux. The reaction solution was concentrated, and then to a solution of the resulting residue in tetrahydrofuran (50 mL) were added (Boc)2O (2.11 g) and triethylamine (1.6 mL), and the mixture was stirred at room temperature for 24 hours. The reaction solution was concentrated, and then the resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (0.35 g).
LC-MS ([M+H]+/Rt (min)): 443.4/1.085
To a solution of the compound of Reference Example 40-3 (0.35 g) in tetrahydrofuran (10 mL) was added 5 mol/L aqueous sodium hydroxide solution (0.5 mL) with ice-cooling, and the mixture was stirred at room temperature for 24 hours. The reaction solution was concentrated, and then the resulting residue was dissolved in ethyl acetate and washed with water and brine. The resulting organic phase was dried over anhydrous magnesium sulfate, filtered, and then concentrated in vacuo to give the title compound (0.26 g).
LC-MS ([M+H]+/Rt (min)): 343.2/0.697
To a solution of the compound of Reference Example 40-4 (0.07 g) in DMF (1 mL) were added sodium carbonate (0.03 g) and benzyl bromide (0.04 g), and the mixture was stirred at 100° C. for 4 hours. The reaction solution was concentrated, and then the resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (0.03 g).
LC-MS ([M+H]+/Rt (min)): 433.4/0.903
According to the process of Reference Example 40-5, the compounds of Reference Examples 41 to 62 were prepared from the compound of Reference Example 40-4 and the corresponding starting compounds.
According to the process of Reference Example 40-2, the title compound was prepared from the compounds of Reference Examples 39-5 and 40-1.
LC-MS ([M+H]+/Rt (min)): 474.4/1.012
According to the process of Reference Example 40-3, the title compound was prepared from the compound of Reference Example 63-1.
According to the process of Reference Example 40-4, the title compound was prepared from the compound of Reference Example 63-2.
LC-MS ([M+H]+/Rt (min)): 344.2/0.572
According to the process of Reference Example 40-5, the compounds of Reference Examples 64 to 88 were prepared from the compound of Reference Example 63-3 and the corresponding starting compounds.
To a solution of 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline (0.98 g) in DMF (10 mL) were added palladium acetate (0.09 g), copper acetate (1.40 g), lithium acetate dihydrate (0.78 g) and methyl acrylate (334 μL), and the mixture was stirred at 100° C. for 4 hours. The reaction solution was concentrated, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (0.46 g).
LC-MS ([M+H]+/Rt (min)): 214.1/0.475
To a solution of the compound of Reference Example 89-1 (0.46 g) in acetic acid (1 mL) was added sodium borohydride (0.10 g), and the mixture was stirred at room temperature for 30 minutes. The reaction solution was basified with saturated aqueous sodium hydrogen carbonate solution, THF (10 mL) and Boc2O (0.49 g) were added thereto, and then the mixture was stirred at room temperature for 16 hours. The reaction solution was diluted with ethyl acetate, washed with water and brine, dried over anhydrous sodium sulfate, filtered, and then concentrated. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (0.03 g).
LC-MS ([M+H]+/Rt (min)): 318.2/1.103
To a solution of the compound of Reference Example 89-2 (0.03 g) in THF (4 mL) and water (1 mL) was added lithium hydroxide (0.01 g) with ice-cooling, and the mixture was stirred at room temperature for 13 hours. The reaction solution was diluted with saturated aqueous sodium hydrogen carbonate solution and washed with diethyl ether. The resulting aqueous phase was acidified with sodium hydrogen sulfate and then extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and then concentrated to give the title compound (0.03 g).
LC-MS ([M-H]−/Rt (min)): 302.5/0.916
According to the process of Reference Example 3, the title compound was prepared from the corresponding starting compound.
LC-MS ([M+H]+/Rt (min)): 513.0/1.084
According to the process of Reference Example 40-5, the compounds of Reference Examples 90 to 98 were prepared from the compound of Reference Example 63-3 and the corresponding starting compounds.
To a solution of the compound of Reference Example 3 (1.5 g) in methanol (40 mL) was added 4 mol/L dioxane hydrochloride (2.97 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo, and then water and 2 mol/L aqueous sodium hydroxide solution were added thereto. The resulting precipitate was collected on a filter, washed with water and hexane/ethyl acetate (2/1), and dried in vacuo to give the title compound (0.89 g).
LC-MS ([M+H]+/Rt (min)): 405.2/0.665
1H-NMR (400 MHz, DMSO-d6) :δ 9.27 (1H, s), 7.96-7.93 (2H, m), 7.69 (1H, d, J=8.0 Hz), 7.43-7.34 (2H, m), 6.91 (1H, d, J=11.6 Hz), 5.23 (2H, s), 3.75 (2H, s), 2.90-2.86 (2H, m), 2.62-2.57 (2H, m).
According to the process of Example 1, the compounds of Examples 2 to 3 were prepared from the corresponding compounds of each Reference Example.
1H-NMR (400 MHz, DMSO-d6): 9.28 (1H, s), 7.96-7.93 (2H, m), 7.71 (1H, d, J = 7.6 Hz), 7.53-7.42 (2H, m), 7.22-7.18 (1H, m), 6.93 (1H, d, J = 10.8 Hz), 5.24 (2H, s), 3.78 (2H, s), 2.93-2.89 (2H, m), 2.65-2.59 (2H, m). LC-MS: [M + H]+/Rt (min): 387.0/0.660
1H-NMR (400 MHz, DMSO-d6): 9.30 (1H, s), 8.02 (1H, s), 7.97 (1H, s), 7.96 (1H, s), 7.88 (1H, s), 7.43-7.37 (2H, m), 5.23 (2H, s), 3.78 (2H, s), 2.92-2.88 (2H, m), 2.71-2.66 (2H, m). LC-MS: [M + H]+/Rt (min): 388.2/0.601
To a solution of the compound of Reference Example 4 (75 mg) in methanol (5 mL) was 4 mol/L dioxane hydrochloride (0.12 mL), and the mixture was stirred at 80° C. The resulting precipitate was collected on a filter, washed with diisopropyl ether, and then dried in vacuo to give the title compound (35.8 mg).
LC-MS ([M+H]−/Rt (min)): 387.2/0.615
According to the process of Example 4, the compounds of Examples 5 to 15 were prepared from the corresponding compounds of each Reference Example.
1H-NMR (400 MHz, CD3OD): 8.94 (1H, d, J = 1.6 Hz), 7.78 (1H, s), 7.65 (1H, d, J = 9.2 Hz), 7.58 (1H, d, J = 2.0 Hz), 7.33-7.30 (2H, m), 5.44 (2H, s), 4.46 (2H, s), 3.56 (2H, t, J = 6.4 Hz), 3.24 (2H, t, J = 6.0 Hz). LC-MS ([M + H]+/Rt (min)): 405.2/0.645
1H-NMR (400 MHz, CD3OD): 8.89 (1H, d, J = 2.0 Hz), 7.87 (2H, m), 7.55 (1H, d, J = 2.0 Hz), 7.42 (1H, d, J = 8.4 Hz), 7.33-7.27 (2H, m), 5.43 (2H, s), 4.46 (2H, s), 3.56 (2H, t, J = 6.4 Hz), 3.22 (2H, t, J = 6.4 Hz). LC-MS ([M + H]+/Rt (min)): 387.2/0.635
1H-NMR (400 MHz, CD3OD): 7.77 (1H, d, J = 6.8 Hz), 7.58 (1H, s), 7.27-7.22 (4H, m), 5.37 (2H, s), 4.44 (2H, s), 3.54 (2H, t, J = 6.4 Hz), 3.16 (2H, t, J = 6.4 Hz). LC-MS([M + 2H]2+/Rt (min)): 203.1/0.620
1H-NMR (400 MHz, CD3OD): 8.90 (1H, d, J = 1.6 Hz), 8.61 (1H, s), 8.17 (1H, s), 7.65 (1H, d, J = 1.6 Hz), 7.35-7.28 (2H, m), 5.43 (2H, s), 4.54 (2H, s), 3.58 (2H, t, J = 6.4 Hz), 3.26 (2H, t, J = 6.4 Hz). LC-MS ([M + H]+/Rt (min)): 388.2/0.554
1H-NMR (400 MHz, CD3OD): 8.94 (1H, s), 8.60 (1H, s), 8.12 (1H, s), 7.82 (1H, s), 7.76-7.65 (4H, m), 5.55 (2H, s), 4.53 (2H, s), 3.58 (2H, t, J = 5.2 Hz), 3.26 (2H, t, J = 6.4 Hz) LC-MS [M + 2H]2+/Rt (min)): 201.7/0.659
1H-NMR (400 MHz, CD3OD): 8.84 (1H, s), 8.12 (1H, d, J = 8.4 Hz), 7.91 (1H, d, J = 8.4 Hz), 7.81 (1H, s), 7.75-7.64 (4H, m), 5.54 (2H, s), 4.53 (2H, s), 3.69 (2H, t, J = 6.4 Hz), 3.36 (2H, t, J = 6.4 Hz). LC-MS ([M + 2H]2+/Rt (min)): 201.7/0.620
1H-NMR (400 MHz, CD3OD): 8.80 (1H, d, J = 1.6 Hz), 8.13 (1H, d, J = 8.0 Hz), 7.92 (1H, d, J = 8.4 Hz), 7.67 (1H, d, J = 2.0 Hz), 7.33-7.26 (2H, m), 5.42 (2H, s), 4.54 (2H, s), 3.70 (2H, t, J = 6.4 Hz), 3.37 (2H, t, J = 6.4 H). LC-MS: [M + 2H]2+/Rt (min): 194.7/0.636
1H-NMR (400 MHz, CD3OD): 9.03 (1H, s), 9.00 (1H, s), 8.31 (1H, s), 7.61 (1H, s), 7.32 (2H, t, J = 7.2 Hz), 5.44 (2H, s), 4.50 (2H, s), 3.61 (2H, t, J = 6.4 Hz), 3.26 (2H, t, J = 6.4 Hz). LC-MS: [M + 2H]2+/Rt (min): 194.7/0.624
1H-NMR (400 MHz, CD3OD): 9.00 (1H, d, J = 2.4 Hz), 8.76 (1H, s), 8.26 (1H, d, J = 1.6 Hz), 7.78-7.57 (4H, m), 7.56 (1H, d, J = 0.8 Hz), 5.51 (2H, s), 4.48 (2H, s), 3.60 (2H, t, J = 6.4 Hz), 3.24 (2H, t, J = 6.4 Hz).
1H-NMR (400 MHz, CD3OD): 8.72 (1H, s), 7.77 (1H, t, J = 7.6 Hz), 7.59 (1H, d, J = 1.2 Hz), 7.29-7.24 (3H, m), 5.39 (2H, s), 4.47 (2H, s), 3.58 (2H, t, J = 6.4 Hz), 3.15 (2H, t, J = 6.4 Hz). LC-MS: [M + 2H]2+/Rt (min): 203.1/0.650
1H-NMR (400 MHz, CD3OD): 8.83 (1H, s), 7.80-7.61 (5H, m), 7.59 (1H, d, J = 1. 2 Hz), 7.24 (1H, d, J = 7.6 Hz), 5.52 (2H, s), 4.47 (2H, s), 3.58 (2H, t, J = 6.4 Hz), 3.15 (2H, t, J = 6.4 Hz). LC-MS: [M + 2H]2+/Rt (min): 210.1/0.708
According to the process of Reference Example 3, the corresponding intermediates of Examples 16 to 17 were synthesized, and then the compounds of Examples 16 to 17 were prepared from the corresponding intermediates according to the process of Example 4 without purification.
According to the process of Example 4, the compounds of Examples 18 to 22 were prepared from the corresponding compounds of each Reference Example.
1H-NMR (400 MHz, CD3OD): 8.93 (1H, s), 7.91-7.88 (2H, m), 7.78-7.60 (4H, m), 7.42 (1H, d, J = 8.0 Hz), 5.57 (2H, s), 4.47 (2H, s), 3.56 (2H, t, J = 6.4 Hz), 3.22 (2H, t, J = 6.4 Hz), 2.21 (3H, d, J = 1.2 Hz). LC-MS: [M + 2H]2+/Rt (min): 208.2/0.668
1H-NMR (400 MHz, CD3OD): 7.88-7.85 (2H, m), 7.75-7.73 (2H, m), 7.68-7.60 (2H, m), 7.42-7.38 (2H, m), 5.49 (2H, s), 4.46 (2H, s), 3.55 (2H, t, J = 6.4 Hz), 3.21 (2H, t, J = 6.0 Hz), 2.68 (3H, d, J = 2.4 Hz). LC-MS: [M + 2H]2+/Rt (min): 208.2/0.583
According to the process of Reference Example 3, the compounds of Examples 23 to 24 were prepared from the corresponding compounds of each Reference Example and the corresponding starting compounds.
To a solution of the compound of Reference Example 28 (103 mg) in chloroform (9 mL) was added trifluoroacetic acid (1 mL), and the mixture was stirred at room temperature for 5 hours. The reaction mixture was concentrated in vacua, to the residue was added a mixed solvent of hexane-ethyl acetate, and the mixture was stirred at room temperature for 1 hour. The resulting precipitate was collected on a filter and dried in vacuo to give the title compound (91 mg).
LC-MS ([M+2H]2−/Rt (min)): 194.1/0.580
1H-NMR (400 MHz, CDCl :δ 7.94 (1H, d, J=1.6 Hz), 7.85-7.83 (2H, m), 7.47 (d, 1H, J=2.0 Hz), 7.38 (d, 1H, J=8.4 Hz), 7.14 (dd, 2H, J=8.4, 6.8 Hz), 5.26 (s, 2H), 4.44 (s, 2H), 3.55 (t, 2H, J=6.4 Hz), 3.20 (t, 2H, J=6.4 Hz).
According to the process of Example 25, the compounds of Examples 26 to 29 were prepared from the corresponding compounds of each Reference Example.
To a solution of the compound of Example 26 (33 mg) in THF (1 mL) were added aqueous formaldehyde solution (1 mL) and sodium triacetoxyborohydride (23 mg), and the mixture was stirred at room temperature for 19 hours. The reaction mixture was concentrated in vacuo, and the residue was dissolved in chloroform, washed with saturated aqueous sodium bicarbonate solution and brine, dried over anhydrous sodium sulfate, filtered, and then concentrated in vacuo. The resulting residue was purified by silica gel column chromatography (chloroform/methanol) to give the title compound (12 mg).
LC-MS ([M+H]+/Rt (min)): 415.6/0.575
A suspension of the compound of Example 25 (80 mg) in ethyl acetate (100 mL) was washed with saturated aqueous sodium bicarbonate solution, and the resulting organic layer was dried over anhydrous sodium sulfate and then concentrated in vacuo to give the title compound (50 mg).
LC-MS ([M+2H]2+/Rt (min)): 194.1/0.580
According to the process of Example 31, the compounds of Examples 32 to 34 were prepared from the corresponding compounds of each Reference Example.
To a solution of the compound of Reference Example 33 (111 mg) in methanol (4 mL) was added 4 mol/L dioxane hydrochloride (1.66 mL), and the mixture was stirred at room temperature overnight. The mixture was then stirred at 50° C. for 6 hours. The reaction mixture was concentrated in vacuo, and then water and 2 mol/L aqueous sodium hydroxide solution were added thereto. The resulting precipitate was collected on a filter and washed with water and hexane/ethyl acetate (2/1). The resulting crude product was purified by amino silica gel column chromatography (chloroform/methanol) to give the title compound (29.5 mg).
LC-MS ([M+H]|/Rt (min)): 370.2/0.618
H-NMR (400 MHz, DMSO-d6) : 9.31 (1H, s), 8.02-7.97 (3H, m), 7.90 (1H, s), 7.57-7.41 (2H, m), 7.25-7.21 (2H, m), 5.26 (2H, s), 3.79 (2H, s), 2.93-2.89 (2H, m), 2.72-2.68 (2H, m).
According to the process of Reference Example 3, the compounds of Examples 36 to 42 were prepared from the corresponding compounds of each Reference Example.
According to the process of Example 4, the compounds of Examples 43 to 70 were prepared from the corresponding compounds of each Reference Example.
According to the process of Example 1, the compounds of Examples 71 to 93 were prepared from the corresponding compounds of each Reference Example (Example).
According to process of Example 1 or 4, the compounds of Examples 94 to 107 were prepared from the corresponding compounds of each Reference Example.
To a solution of the compound of Example 26 (0.03 g) in THF (1 mL) were added pyridine (25 μL) and acetic anhydride (12 μL), and the mixture was stirred at room temperature for 3 hours. The reaction solution was concentrated, and then the residue was purified by reverse-phase HPLC (mobile phase: 0.05% TFA/water and 0.035% TFA/acetonitrile) to give the title compound (0.02 g).
LC-MS ([M+H]+/Rt (min)): 443.3/0.825
According to the process of Reference Example 3, the title compound was prepared from the compound of Reference Example 11-2 and the compound described in U.S. Pat. No. 5,786,356.
LC-MS ([M+H]+/Rt (min)): 458.4/0.870
A solution of the compound of Example 109 (0.20 g) in a mixed solvent of 4 mol/L dioxane hydrochloride (4 mL) and water (1 mL) was stirred at room temperature for 20 hours. The reaction solution was diluted with ethyl acetate, and then washed with saturated aqueous sodium hydrogen carbonate and brine. The organic phase was dried over anhydrous sodium sulfate, filtered, and then concentrated in vacuo. The resulting residue was purified by silica gel column chromatography (chloroform/methanol) to give the title compound (0.15 g).
LC-MS ([M+H]+/Rt (min)): 414.2/0.805
To a solution of the compound of Example 110 (0.06 g) in methanol was added sodium borohydride (0.01 g) with ice-cooling, and then the mixture was stirred at room temperature for 1 hour. The reaction solution was diluted with ethyl acetate and then washed with water and brine. The organic phase was dried over anhydrous sodium sulfate, filtered, and then concentrated in vacuo. The resulting residue was purified by silica gel column chromatography (chloroform/methanol) to give the title compound (0.06 g).
LC-MS ([M+H]+/Rt (min)): 416.3/0.754
According to the process of Example 4, the compounds of Examples 112 to 121 were prepared from the corresponding compounds of each Reference Example.
The reliable methods established for measuring the self-renewal ability of cells which is one of the CSC's properties include a method for measuring the sphere-forming ability of cancer cells in non-adherent condition in the absence of serum (Cancer Res 65, 5506-5511 (2005)). HCT-116 cells were available from the American Type Culture Collection (ATCC). HCT-116 cells were cultured at 37° C. and 5% CO2 using the McCoy's 5a medium containing 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin. HCT-116 cells were seeded in a 384 Well Black Clear Bottom Ultra-Low Attachment Microplate (Corning Cat. No.3827) in an amount of 350-800 cells/well using the DMEM/F12 medium containing 2% B27 supplement (GIBCO), 20 ng/mL epidermal growth factor (EGF) (peprotech), 10 ng/mL basic fibroblast growth factor (bFGF) (peprotech), 5 μg/mL insulin (Sigma), and 1% penicillin/streptomycin. The test compounds were added into each well to adjust the final concentration of DMSO to 0.1%, and the cells were cultured for 4 days. The number of viable cells in each well was then measured with CellTiter-Glo® Luminescent Cell Viability Assay (Promega) to calculate the concentration of each test compound for 50% inhibition of cell proliferation (Sphere IC50 value; μmol/L).
The experiment of Test Example 1 was performed for the compounds of each Example. The concentrations of each test compound for 50% inhibition of cell profeliration (Sphere IC50 value; μmol/L) are shown in the following Table.
HCT-116 cells were available from the American Type Culture Collection (ATCC). HCT-116 cells were cultured at 37° C. and 5% CO2 using the McCoy's 5a medium containing 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin. HCT-116 cells were seeded in a 384 Well Black Clear Bottom Ultra-Low Attachment Microplate (Corning Cat. No.3827) in an amount of 350-800 cells/well using the DMEM/F12 medium containing 2% B27 supplement (GIBCO), 20 ng/mL epidermal growth factor (EGF) (peprotech), 10 ng/mL basic fibroblast growth factor (bFGF) (peprotech), 5 μg/mL insulin (Sigma), 5% bovine serum albumin (BSA), and 1% penicillin/streptomycin. The test compounds were added into each well to adjust the final concentration of DMSO to 0.1%, and the cells were cultured for 4 days. The number of viable cells in each well was then measured with CellTiter-Glo® Luminescent Cell Viability Assay (Promega) to calculate the concentration of each test compound for 50% inhibition of cell proliferation (Sphere IC50 value; μmol/L).
The experiment of Test Example 2 was performed for the compounds of each Example. The concentrations of each test compound for 50% inhibition of cell profeliration (Sphere IC50 value; μmol/L) are shown in the following Table.
A 7-week-old mouse (BALB/cAnNCrlCrlj, female, CHARLES RIVER LABORATORIES JAPAN, INC.) receives single oral administration of each compound suspended in 0.5% methylcellulose solution in a dose of 10 mg/kg or 100 mg/kg. Blood is collected from the mouse 0.5, 1, 2, 4, 8 and 24 hours after the administration, and plasma from the blood is collected by centrifugation. The area under the plasma concentration-time curve (AUC) is calculated on the basis of the concentration changes to calculate the bioavailability of each compound according to the following formula:
Bioavailabity (%)=AUC after oral administration/AUC after intravenous administration×100
Plasma is deproteinized by adding methanol at the final concentration of 80%, centrifuging the methanol solution, and filtrating the contrifuged solution, and then the present compound in the deproteinized plasma is detected and quantified with an LC-MS/MS (API4000, AB SCIEX). When the present compound is quantified, a calibration curve is prepared based on the mouse plasma added with a given amount of the compound. Bezafibrate is used as internal standard.
The present compound can be used to evaluate the anti-tumor effect thereof A 4 to 7-week-old nude mouse (BALB/cAnNCrj-nu/nu, female, CHARLES RIVER LABORATORIES JAPAN, INC.) received intradermal transplantation of HCT-116 cells (ATCC) in an amount of 3×106 cells/mouse around the ventral portion. The engraftment of HCT-116 cells was observed 5 to 14 days after the transplantation, and then each compound suspended in a solvent such as 0.5% methylcellulose solution was orally administrated to the mouse in a dose of 1 to 100 mg/kg one to twice daily. The tumor volume was measured over time after the administration to evaluate the effect for reducing the tumor volume by the administration of each compound. The tumor volume can be calculated from the minor axis and the major axis of the tumor measured with a digital caliper (Mitutoyo) according to the following formula:
Tumor volume [mm3]=0.5×minor axis [mm]×(major axis [mm])2
The tumor volume in control administration group treated with only a solvent such as 0.5% methylcellulose solution was compared with that of the present compound administration group, and T/C value was calculated according the following formula to evaluate the anti-tumor effect of the present compound.
T/C(%)=(the tumor volume at the end of administration in the present compound administration group−the tumor volume at the start of administration in the present compound administration group)/(the tumor volume at the end of administration in the control administration group−the tumor volume at the start of administration in the the control administration group)×100
The T/C values (%) of the present compound on each dosage and administration period in the HCT-116 tumor-bearing mouse are shown below.
The present compound has a potent inhibitory effect on sphere-forming ability of cancer cells, and is useful as an orally-available anti-cancer agent.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2015-125175 | Jun 2015 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2016/068424 | 6/21/2016 | WO | 00 |
