JP2007503450A - 置換２，３−ジヒドロ−１ｈ−イソインドル−１−オン誘導体及び使用方法 - Google Patents

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Publication number

JP2007503450A

JP2007503450A JP2006524818A JP2006524818A JP2007503450A JP 2007503450 A JP2007503450 A JP 2007503450A JP 2006524818 A JP2006524818 A JP 2006524818A JP 2006524818 A JP2006524818 A JP 2006524818A JP 2007503450 A JP2007503450 A JP 2007503450A

Authority

JP

Japan

Prior art keywords

phenyl

dihydro

optionally substituted

amino

ylmethyl

Prior art date

2003-08-25

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Withdrawn

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• 238000000034 method Methods 0.000 title claims abstract description 57
• PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical class C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 title 1
• 150000001875 compounds Chemical class 0.000 claims abstract description 257
• 238000011282 treatment Methods 0.000 claims abstract description 40
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 38
• 206010028980 Neoplasm Diseases 0.000 claims abstract description 32
• 230000033115 angiogenesis Effects 0.000 claims abstract description 20
• 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 9
• 201000011510 cancer Diseases 0.000 claims abstract description 8
• -1 —OR 3 Chemical group 0.000 claims description 1023
• 125000000623 heterocyclic group Chemical group 0.000 claims description 143
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 112
• 125000000217 alkyl group Chemical group 0.000 claims description 79
• 125000001424 substituent group Chemical group 0.000 claims description 69
• 238000002360 preparation method Methods 0.000 claims description 61
• 125000005843 halogen group Chemical group 0.000 claims description 53
• 125000002757 morpholinyl group Chemical group 0.000 claims description 40
• 150000003839 salts Chemical class 0.000 claims description 37
• 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims description 36
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 35
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 34
• 125000004043 oxo group Chemical group O=* 0.000 claims description 34
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 33
• 125000006559 (C1-C3) alkylamino group Chemical group 0.000 claims description 30
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 30
• 239000003814 drug Substances 0.000 claims description 28
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 26
• 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims description 26
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 26
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 25
• 125000004484 1-methylpiperidin-4-yl group Chemical group CN1CCC(CC1)* 0.000 claims description 22
• 239000003795 chemical substances by application Substances 0.000 claims description 22
• 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 22
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 22
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 21
• 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 21
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 21
• 125000003545 alkoxy group Chemical group 0.000 claims description 20
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 20
• 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 20
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 19
• 125000001153 fluoro group Chemical group F* 0.000 claims description 19
• 229910052739 hydrogen Inorganic materials 0.000 claims description 18
• 125000001072 heteroaryl group Chemical group 0.000 claims description 17
• 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 16
• 125000001462 1-pyrrolyl group Chemical group [*]N1C([H])=C([H])C([H])=C1[H] 0.000 claims description 16
• 125000004485 2-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])C1([H])* 0.000 claims description 16
• 125000003418 alkyl amino alkoxy group Chemical group 0.000 claims description 16
• 125000004567 azetidin-3-yl group Chemical group N1CC(C1)* 0.000 claims description 16
• 125000001188 haloalkyl group Chemical group 0.000 claims description 16
• 229910052799 carbon Inorganic materials 0.000 claims description 15
• 208000035475 disorder Diseases 0.000 claims description 15
• 229940079593 drug Drugs 0.000 claims description 15
• 125000005956 isoquinolyl group Chemical group 0.000 claims description 15
• 229920006395 saturated elastomer Polymers 0.000 claims description 15
• 125000000389 2-pyrrolyl group Chemical group [H]N1C([*])=C([H])C([H])=C1[H] 0.000 claims description 14
• 125000005246 nonafluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 claims description 14
• 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 13
• 125000002883 imidazolyl group Chemical group 0.000 claims description 13
• 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 claims description 13
• 229910052760 oxygen Inorganic materials 0.000 claims description 12
• 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims description 11
• 125000003342 alkenyl group Chemical group 0.000 claims description 11
• 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 11
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 11
• 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 10
• 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 10
• 238000006467 substitution reaction Methods 0.000 claims description 10
• 230000012010 growth Effects 0.000 claims description 9
• 229910052717 sulfur Inorganic materials 0.000 claims description 9
• 125000000041 C6-C10 aryl group Chemical group 0.000 claims description 8
• KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 8
• 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 8
• 125000005493 quinolyl group Chemical group 0.000 claims description 8
• 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 8
• 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims description 7
• 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 7
• 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 7
• 108010050904 Interferons Proteins 0.000 claims description 7
• 102000014150 Interferons Human genes 0.000 claims description 7
• SZPWXAOBLNYOHY-UHFFFAOYSA-N [C]1=CC=NC2=CC=CC=C12 Chemical group [C]1=CC=NC2=CC=CC=C12 SZPWXAOBLNYOHY-UHFFFAOYSA-N 0.000 claims description 7
• 125000000278 alkyl amino alkyl group Chemical group 0.000 claims description 7
• 229940079322 interferon Drugs 0.000 claims description 7
• 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 7
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 7
• 125000003226 pyrazolyl group Chemical group 0.000 claims description 7
• 125000004076 pyridyl group Chemical group 0.000 claims description 7
• 125000003070 2-(2-chlorophenyl)ethyl group Chemical group [H]C1=C([H])C(Cl)=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 6
• 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 6
• 241001465754 Metazoa Species 0.000 claims description 6
• 125000000304 alkynyl group Chemical group 0.000 claims description 6
• 239000003242 anti bacterial agent Substances 0.000 claims description 6
• 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 6
• 125000002541 furyl group Chemical group 0.000 claims description 6
• 125000003884 phenylalkyl group Chemical group 0.000 claims description 6
• 125000004940 pyridazin-4-yl group Chemical group N1=NC=C(C=C1)* 0.000 claims description 6
• 125000004942 pyridazin-6-yl group Chemical group N1=NC=CC=C1* 0.000 claims description 6
• 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims description 6
• 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims description 6
• 125000004943 pyrimidin-6-yl group Chemical group N1=CN=CC=C1* 0.000 claims description 6
• 206010012689 Diabetic retinopathy Diseases 0.000 claims description 5
• 206010061218 Inflammation Diseases 0.000 claims description 5
• 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 5
• 230000004054 inflammatory process Effects 0.000 claims description 5
• 125000002971 oxazolyl group Chemical group 0.000 claims description 5
• 125000001544 thienyl group Chemical group 0.000 claims description 5
• KPPVNWGJXFMGAM-UUILKARUSA-N (e)-2-methyl-1-(6-methyl-3,4-dihydro-2h-quinolin-1-yl)but-2-en-1-one Chemical compound CC1=CC=C2N(C(=O)C(/C)=C/C)CCCC2=C1 KPPVNWGJXFMGAM-UUILKARUSA-N 0.000 claims description 4
• BMBGBJAMLUTSGP-UHFFFAOYSA-N 2-(4,4-dimethyl-2,3-dihydro-1h-isoquinolin-7-yl)-7-(quinolin-6-ylmethylamino)-3h-isoindol-1-one Chemical compound N1=CC=CC2=CC(CNC=3C=CC=C4CN(C(C4=3)=O)C=3C=C4CNCC(C4=CC=3)(C)C)=CC=C21 BMBGBJAMLUTSGP-UHFFFAOYSA-N 0.000 claims description 4
• MQRHEYRJEXDUDI-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-1-hydroxy-4-(pyridin-4-ylmethylamino)-1h-pyrrolo[3,4-c]pyridin-3-one Chemical compound C1=CC(C(C)(C)C)=CC=C1N1C(=O)C2=C(NCC=3C=CN=CC=3)N=CC=C2C1O MQRHEYRJEXDUDI-UHFFFAOYSA-N 0.000 claims description 4
• MCPKAZGMSPNARI-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound C1=CC(C(C)(C)C)=CC=C1N1C(=O)C2=C(NCC=3C=CN=CC=3)C=CC=C2C1 MCPKAZGMSPNARI-UHFFFAOYSA-N 0.000 claims description 4
• YGNPYFDHDYUVBN-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-7-[[2-(methylamino)pyrimidin-4-yl]methylamino]-3h-isoindol-1-one Chemical compound CNC1=NC=CC(CNC=2C=3C(=O)N(CC=3C=CC=2)C=2C=CC(=CC=2)C(C)(C)C)=N1 YGNPYFDHDYUVBN-UHFFFAOYSA-N 0.000 claims description 4
• 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims description 4
• 241000124008 Mammalia Species 0.000 claims description 4
• 230000000340 anti-metabolite Effects 0.000 claims description 4
• 229940100197 antimetabolite Drugs 0.000 claims description 4
• 239000002256 antimetabolite Substances 0.000 claims description 4
• 230000003115 biocidal effect Effects 0.000 claims description 4
• 125000000392 cycloalkenyl group Chemical group 0.000 claims description 4
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
• 239000003937 drug carrier Substances 0.000 claims description 4
• 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 claims description 4
• 125000006517 heterocyclyl carbonyl group Chemical group 0.000 claims description 4
• 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 4
• 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 4
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
• 125000004497 pyrazol-5-yl group Chemical group N1N=CC=C1* 0.000 claims description 4
• 125000002098 pyridazinyl group Chemical group 0.000 claims description 4
• 125000000168 pyrrolyl group Chemical group 0.000 claims description 4
• 125000000335 thiazolyl group Chemical group 0.000 claims description 4
• OHKXAAYXNGNVSQ-UHFFFAOYSA-N 2-(1-acetyl-3,3-dimethyl-2h-indol-6-yl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound C1=C2N(C(=O)C)CC(C)(C)C2=CC=C1N(C(C1=2)=O)CC1=CC=CC=2NCC1=CC=NC=C1 OHKXAAYXNGNVSQ-UHFFFAOYSA-N 0.000 claims description 3
• AMMJYZHEPBAGLM-UHFFFAOYSA-N 2-(3,3-dimethyl-1,2-dihydroindol-6-yl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound C=1C=C2C(C)(C)CNC2=CC=1N(C(C1=2)=O)CC1=CC=CC=2NCC1=CC=NC=C1 AMMJYZHEPBAGLM-UHFFFAOYSA-N 0.000 claims description 3
• NTYRKOGMBINLQW-UHFFFAOYSA-N 2-(4,4-dimethyl-2,3-dihydro-1h-isoquinolin-7-yl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound C=1C=C2C(C)(C)CNCC2=CC=1N(C(C1=2)=O)CC1=CC=CC=2NCC1=CC=NC=C1 NTYRKOGMBINLQW-UHFFFAOYSA-N 0.000 claims description 3
• SPYMLDYBWRGZHY-UHFFFAOYSA-N 2-(4-phenylphenyl)-4-(pyridin-4-ylmethylamino)-1h-pyrrolo[3,4-c]pyridin-3-one Chemical compound C=12C(=O)N(C=3C=CC(=CC=3)C=3C=CC=CC=3)CC2=CC=NC=1NCC1=CC=NC=C1 SPYMLDYBWRGZHY-UHFFFAOYSA-N 0.000 claims description 3
• IXWUZSMDRFSELS-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-3-hydroxy-3-methyl-7-(pyridin-4-ylmethylamino)isoindol-1-one Chemical compound C1=CC(C(C)(C)C)=CC=C1N1C(O)(C)C(C=CC=C2NCC=3C=CN=CC=3)=C2C1=O IXWUZSMDRFSELS-UHFFFAOYSA-N 0.000 claims description 3
• FCVVOQIBIJMINM-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-3-methyl-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound CC1N(C=2C=CC(=CC=2)C(C)(C)C)C(=O)C2=C1C=CC=C2NCC1=CC=NC=C1 FCVVOQIBIJMINM-UHFFFAOYSA-N 0.000 claims description 3
• UIYWWRCGMKAGAZ-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-7-(1h-pyrrolo[2,3-b]pyridin-3-ylmethylamino)-3h-isoindol-1-one Chemical compound C1=CC(C(C)(C)C)=CC=C1N1C(=O)C2=C(NCC=3C4=CC=CN=C4NC=3)C=CC=C2C1 UIYWWRCGMKAGAZ-UHFFFAOYSA-N 0.000 claims description 3
• UZQVJYCBNKOQAK-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-7-(2-pyridin-2-ylethenyl)-3h-isoindol-1-one Chemical compound C1=CC(C(C)(C)C)=CC=C1N1C(=O)C2=C(C=CC=3N=CC=CC=3)C=CC=C2C1 UZQVJYCBNKOQAK-UHFFFAOYSA-N 0.000 claims description 3
• DBPFYZDHXXIPDK-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-7-(pyridin-4-ylmethoxy)-3h-isoindol-1-one Chemical compound C1=CC(C(C)(C)C)=CC=C1N1C(=O)C2=C(OCC=3C=CN=CC=3)C=CC=C2C1 DBPFYZDHXXIPDK-UHFFFAOYSA-N 0.000 claims description 3
• ZRFIAPFXVAQONQ-QGZVFWFLSA-N 2-(4-tert-butylphenyl)-7-[(1r)-1-pyridin-4-ylethoxy]-3h-isoindol-1-one Chemical compound O([C@H](C)C=1C=CN=CC=1)C(C=1C2=O)=CC=CC=1CN2C1=CC=C(C(C)(C)C)C=C1 ZRFIAPFXVAQONQ-QGZVFWFLSA-N 0.000 claims description 3
• ZRFIAPFXVAQONQ-KRWDZBQOSA-N 2-(4-tert-butylphenyl)-7-[(1s)-1-pyridin-4-ylethoxy]-3h-isoindol-1-one Chemical compound O([C@@H](C)C=1C=CN=CC=1)C(C=1C2=O)=CC=CC=1CN2C1=CC=C(C(C)(C)C)C=C1 ZRFIAPFXVAQONQ-KRWDZBQOSA-N 0.000 claims description 3
• QZLCBACRZQPASX-UHFFFAOYSA-N 2-(5-tert-butyl-1h-pyrazol-3-yl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound N1N=C(C(C)(C)C)C=C1N1C(=O)C2=C(NCC=3C=CN=CC=3)C=CC=C2C1 QZLCBACRZQPASX-UHFFFAOYSA-N 0.000 claims description 3
• UAMCWQXBRGVRRS-UHFFFAOYSA-N 2-[3-(oxolan-3-yloxy)-5-(trifluoromethyl)phenyl]-7-(pyridin-4-ylamino)-3h-isoindol-1-one Chemical compound C=1C(N2C(C3=C(NC=4C=CN=CC=4)C=CC=C3C2)=O)=CC(C(F)(F)F)=CC=1OC1CCOC1 UAMCWQXBRGVRRS-UHFFFAOYSA-N 0.000 claims description 3
• GKECDORWWXXNRY-UHFFFAOYSA-N 2h-pyridin-3-one Chemical compound O=C1CN=CC=C1 GKECDORWWXXNRY-UHFFFAOYSA-N 0.000 claims description 3
• QLWPUIYXTHKZLF-UHFFFAOYSA-N 4-[(2-aminopyridin-4-yl)methylamino]-2-(4-tert-butylphenyl)-1h-pyrrolo[3,4-c]pyridin-3-one Chemical compound C1=CC(C(C)(C)C)=CC=C1N1C(=O)C2=C(NCC=3C=C(N)N=CC=3)N=CC=C2C1 QLWPUIYXTHKZLF-UHFFFAOYSA-N 0.000 claims description 3
• 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims description 3
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
• 125000001041 indolyl group Chemical group 0.000 claims description 3
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
• 125000000714 pyrimidinyl group Chemical group 0.000 claims description 3
• 125000001113 thiadiazolyl group Chemical group 0.000 claims description 3
• 125000004607 1,2,3,4-tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 claims description 2
• 125000005877 1,4-benzodioxanyl group Chemical group 0.000 claims description 2
• ZYEXXLASDABUPX-UHFFFAOYSA-N 2-(2-phenylethyl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound C1C2=CC=CC(NCC=3C=CN=CC=3)=C2C(=O)N1CCC1=CC=CC=C1 ZYEXXLASDABUPX-UHFFFAOYSA-N 0.000 claims description 2
• BTBOMRLNHNZBBU-UHFFFAOYSA-N 2-(3-chlorophenyl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound ClC1=CC=CC(N2C(C3=C(NCC=4C=CN=CC=4)C=CC=C3C2)=O)=C1 BTBOMRLNHNZBBU-UHFFFAOYSA-N 0.000 claims description 2
• KBALXVGDUJNLLE-UHFFFAOYSA-N 2-(3-methylphenyl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound CC1=CC=CC(N2C(C3=C(NCC=4C=CN=CC=4)C=CC=C3C2)=O)=C1 KBALXVGDUJNLLE-UHFFFAOYSA-N 0.000 claims description 2
• FORARFUZEXMMNJ-UHFFFAOYSA-N 2-(3-tert-butylphenyl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound CC(C)(C)C1=CC=CC(N2C(C3=C(NCC=4C=CN=CC=4)C=CC=C3C2)=O)=C1 FORARFUZEXMMNJ-UHFFFAOYSA-N 0.000 claims description 2
• AJIBKXDARQXECE-UHFFFAOYSA-N 2-(4-butan-2-ylphenyl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound C1=CC(C(C)CC)=CC=C1N1C(=O)C2=C(NCC=3C=CN=CC=3)C=CC=C2C1 AJIBKXDARQXECE-UHFFFAOYSA-N 0.000 claims description 2
• JVQNOBVPNMKRMH-UHFFFAOYSA-N 2-(4-butan-2-ylphenyl)-7-[(2-methoxypyridin-4-yl)methylamino]-3h-isoindol-1-one Chemical compound C1=CC(C(C)CC)=CC=C1N1C(=O)C2=C(NCC=3C=C(OC)N=CC=3)C=CC=C2C1 JVQNOBVPNMKRMH-UHFFFAOYSA-N 0.000 claims description 2
• PYKPRWVUSABCJJ-UHFFFAOYSA-N 2-(4-butan-2-ylphenyl)-7-[(4-fluorophenyl)methylamino]-3h-isoindol-1-one Chemical compound C1=CC(C(C)CC)=CC=C1N1C(=O)C2=C(NCC=3C=CC(F)=CC=3)C=CC=C2C1 PYKPRWVUSABCJJ-UHFFFAOYSA-N 0.000 claims description 2
• JJLDBGSGVOCULM-UHFFFAOYSA-N 2-(4-methylphenyl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound C1=CC(C)=CC=C1N1C(=O)C2=C(NCC=3C=CN=CC=3)C=CC=C2C1 JJLDBGSGVOCULM-UHFFFAOYSA-N 0.000 claims description 2
• PIQOJBXOWOQKTG-UHFFFAOYSA-N 2-(4-phenoxyphenyl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound C=12C(=O)N(C=3C=CC(OC=4C=CC=CC=4)=CC=3)CC2=CC=CC=1NCC1=CC=NC=C1 PIQOJBXOWOQKTG-UHFFFAOYSA-N 0.000 claims description 2
• SJRUEPKVLFHWID-UHFFFAOYSA-N 2-(4-phenoxyphenyl)-7-(quinolin-6-ylmethylamino)-3h-isoindol-1-one Chemical compound C1C2=CC=CC(NCC=3C=C4C=CC=NC4=CC=3)=C2C(=O)N1C(C=C1)=CC=C1OC1=CC=CC=C1 SJRUEPKVLFHWID-UHFFFAOYSA-N 0.000 claims description 2
• CPGJXHGLZOOISC-UHFFFAOYSA-N 2-(4-phenyl-1,3-thiazol-2-yl)-7-(pyridin-4-ylmethylamino)-3h-isoindol-1-one Chemical compound C=12C(=O)N(C=3SC=C(N=3)C=3C=CC=CC=3)CC2=CC=CC=1NCC1=CC=NC=C1 CPGJXHGLZOOISC-UHFFFAOYSA-N 0.000 claims description 2
• BXPUHWFOLYYJRL-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-4-(1h-indazol-6-ylamino)-1h-pyrrolo[3,4-c]pyridin-3-one Chemical compound C1=CC(C(C)(C)C)=CC=C1N1C(=O)C2=C(NC=3C=C4NN=CC4=CC=3)N=CC=C2C1 BXPUHWFOLYYJRL-UHFFFAOYSA-N 0.000 claims description 2
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