(1,10B-dihydro-2-(aminoalkyl-phenyl)-5
View Patent ↗The present invention relates to 5H-pyrazolo[1,5-c][1,3]benzoxazin-5-yl)phenyl methanone derivatives as inhibitors of the viral replication of the HIV virus, processes for their preparation as well as pharmaceutical compositions, their use as medicines, and diagnostic kits comprising them. The present invention also concerns combinations of the present HIV inhibitors with other anti-retroviral agents. It further relates to their use in assays as reference compounds or as reagents. The compounds of the present invention are useful for preventing or treating infection by HIV and for treating AIDS.
1. A compound having the formula
a N-oxide, stereoisomeric form or salt thereof,
wherein
a is zero, 1, 2, 3, 4 or 5;
L is C 1-4 alkanediyl;
R 1 is hydrogen, C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-12 cycloalkyl, Het, aryl or C 1-10 alkyl substituted with a substituent selected from the group consisting of Het, aryl, C 3-12 cycloalkyl, amino and mono- or disubstituted amino wherein the substituents on the amino group are each individually selected from C 1-10 alkyl, C 2-10 alkenyl, C 3-12 cycloalkyl, Het and aryl;
R 2 is hydrogen, C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-12 cycloalkyl, Het, aryl or C 1-10 alkyl substituted with a substituent selected from the group consisting of Het, aryl, C 3-12 cycloalkyl, amino and mono- or disubstituted amino wherein the substituents on the amino group are each individually selected from C 1-10 alkyl, C 2-10 alkenyl, C 3-12 cycloalkyl, Het and aryl; or
R 1 and R 2 taken together with the nitrogen atom to which they are attached form a 5 to 12 membered saturated or partially saturated heterocycle with one or more heteroatoms each individually selected from nitrogen, oxygen or sulfur, and wherein said heterocycle may optionally be substituted with C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-12 cycloalkyl, C 1-6 alkyloxycarbonyl, Het, aryl or C 1-10 alkyl substituted with a substituent selected from the group consisting of Het, aryl, C 3-12 cycloalkyl, amino and mono- or disubstituted amino wherein the substituents on the amino group are each individually selected from C 1-10 alkyl, C 2-10 alkenyl, C 3-12 cycloalkyl, Het and aryl;
R 3 is carboxyl, halogen, nitro, C 1-10 alkyl, C 3-12 cycloalkyl, polyhaloC 1-10 alkyl, cyano, amino, mono- or disubstituted amino, aminocarbonyl, mono- or disubstituted aminocarbonyl, C 1-10 alkyloxy, C 1-10 alkylthio, C 1-10 alkylsulfonyl, pyrrolidinyl, piperidinyl, homopiperidinyl, morpholinyl, thiomorpholinyl or piperazinyl optionally substituted with C 1-10 alkyl, wherein the substituents on any of the amino groups are each individually selected from C 1-10 alkyl, C 2-10 alkenyl, C 3-12 cycloalkyl, Het and aryl;
aryl is phenyl optionally substituted with one or more substituents selected from the group consisting of C 1-10 alkyl, polyhaloC 1-10 alkyl, C 1-10 alkyloxy, C 1-10 alkylthio, C 1-10 alkylsulfonyl, nitro, cyano, halo, C 3-7 cycloalkyl, C 1-10 alkylcarbonyl, carboxyl, C 1-10 alkyloxycarbonyl, amino, mono- or disubstituted amino, aminocarbonyl, mono- or disubstituted aminocarbonyl, wherein the substituents on any of the amino groups are each individually selected from phenyl, C 1-10 alkyl, C 2-10 alkenyl, C 3-7 cycloalkyl, pyrrolidinyl, piperidinyl, homopiperidinyl or piperazinyl optionally substituted with C 1-10 alkyl;
Het is a 5 or 6 membered aromatic, saturated or partially saturated, monocyclic heterocycle with one or more heteroatoms each individually selected from nitrogen, oxygen or sulfur, and which heterocycle may optionally be substituted by one, or where possible, more than one substituent selected from the group consisting of C 1-10 alkyl, polyhaloC 1-10 alkyl, C 1-10 alkyloxy, C 1-10 alkylthio, C 1-10 alkylsulfonyl, nitro, cyano, halo, C 3-7 cycloalkyl, C 1-10 alkylcarbonyl, carboxyl, C 1-10 alkyloxycarbonyl, amino, mono- or disubstituted amino, aminocarbonyl, mono- or disubstituted aminocarbonyl, wherein the substituents on any of the amino groups are each individually selected from phenyl, C 1-10 alkyl, C 2-10 alkenyl, C 3-7 cycloalkyl, pyrrolidinyl, piperidinyl, homopiperidinyl or piperazinyl optionally substituted with C 1-10 alkyl.
2. A compound as claimed in claim 1 wherein one or more of the following restrictions apply:
a) a is zero or 1;
b) R 1 is C 1-10 alkyl, C 3-12 cycloalkyl, Het, aryl or C 1-10 alkyl substituted with a substituent selected from the group consisting of Het, aryl, C 3-12 cycloalkyl and mono- or disubstituted amino wherein the substituents on the amino group are each individually selected from C 1-10 alkyl;
c) R 2 is hydrogen, C 1-10 alkyl, C 2-10 alkenyl or C 1-10 alkyl substituted with aryl;
d) R 1 and R 2 taken together with the nitrogen atom to which they are attached form a 5 to 12 membered saturated or partially saturated heterocycle which heterocycle may optionally be substituted with C 1-10 alkyl, C 1-6 alkyloxycarbonyl or C 1-10 alkyl substituted with aryl;
e) L is C 1-2 alkanediyl;
f) R 3 is halogen, nitro, C 1-10 alkyl, C 3-12 cycloalkyl, polyhaloC 1-10 alkyl, cyano, C 1-10 alkyloxy, C 1-10 alkylthio, C 1-10 alkylsulfonyl, piperidinyl, or morpholinyl;
g) aryl is phenyl optionally substituted with one or more substituents selected from the group consisting of C 1-10 alkyloxy, halo, mono- or disubstituted amino, wherein the substituents on any of the amino groups are each individually selected from C 1-10 alkyl;
h) Het is a 5 or 6 membered aromatic, saturated or partially saturated, monocyclic or bicyclic heterocycle with one or more heteroatoms each individually selected from nitrogen, oxygen or sulfur, and which heterocycle may optionally be substituted by C 1-10 alkyl.
3. A compound as claimed in claim 1 having the formula:
4-[2-(4-Diethylaminomethyl-phenyl)-1,9b-dihydro-5-oxa-3,3a-diaza-cyclopenta[a]-
naphthalene-4-carbonyl]-benzonitrile;
4-{2-[4-(Benzylamino-methyl)-phenyl]-1,9b-dihydro-5-oxa-3,3a-diaza-cyclopenta[a]-
naphthalene-4-carbonyl}-benzonitrile;
4-[2-(4-{[(Pyridin-4-ylmethyl)-amino]-methyl}-phenyl)-1,9b-dihydro-5-oxa-3,3a-
diaza-cyclopenta[a]naphthalene-4-carbonyl]-benzonitrile;
4-[2-(4-{[(4-Methoxy-benzyl)-methyl-amino]-methyl}-phenyl)-1,9b-dihydro-5-oxa-
3,3a-diaza-cyclopenta[a]naphthalene-4-carbonyl]-benzonitrile;
(4-tert-Butyl-phenyl)-[2-(4-{[(4-methoxy-benzyl)-methyl-amino]-methyl}-phenyl)-
1,9b-dihydro-5-oxa-3,3a-diaza-cyclopenta[a]naphthalen-4-yl]-methanone;
(4-tert-Butyl-phenyl)-[2-(4-{[(pyridin-4-ylmethyl)-amino]-methyl}-phenyl)-1,9b-
dihydro-5-oxa-3,3a-diaza-cyclopenta[a]naphthalen-4-yl]-methanone;
(4-tert-Butyl-phenyl)-[2-(4-diethylaminomethyl-phenyl)-1,9b-dihydro-5-oxa-3,3a-
diaza-cyclopenta[a]naphthalen-4-yl]-methanone;
4-{2-[4-(2-Diethylamino-ethyl)-phenyl]-1,9b-dihydro-5-oxa-3,3a-diaza-cyclopenta[a]-
naphthalene-4-carbonyl}-benzonitrile;
4-(2-{4-[(Cyclopentyl-methyl-amino)-methyl]-phenyl}-1,9b-dihydro-5-oxa-3,3a-diaza-
cyclopenta[a]naphthalene-4-carbonyl)-benzonitrile;
4-(2-{4-[4-(4-Methoxy-phenylamino)-butyl]-phenyl}-1,9b-dihydro-5-oxa-3,3a-diaza-
cyclopenta[a]naphthalene-4-carbonyl)-benzonitrile;
(4-Methanesulfonyl-phenyl)-[2-(4-{[(pyridin-4-ylmethyl)-amino]-methyl}-phenyl)-
1,9b-dihydro-5-oxa-3,3a-diaza-cyclopenta[a]naphthalen-4-yl]-methanone;
(4-Methanesulfonyl-phenyl)-[2-(4-{[(4-methoxy-benzyl)-methyl-amino]-methyl}-
phenyl)-1,9b-dihydro-5-oxa-3,3a-diaza-cyclopenta[a]naphthalen-4-yl]-methanone;
[2-(4-Diethylaminomethyl-phenyl)-1,9b-dihydro-5-oxa-3,3a-diaza-cyclopenta[a]-
naphthalen-4-yl]-(4-methanesulfonyl-phenyl)-methanone;
or a N-oxide, stereoisomeric form or salt thereof.
4. A method of treatment comprising the systemic administration of an effective therapeutic amount of a compound as claimed in claim 1 to HIV-infected warm-blooded animals, in particular, HIV-infected humans.
5. A pharmaceutical preparation which as active constituents contain an effective dose of a compound as claimed in claim 1 in addition to customary pharmaceutically innocuous excipients and auxiliaries.