ES2821821T3 - Derivados de tetrahidroisoquinolina - Google Patents
Derivados de tetrahidroisoquinolina Download PDFInfo
- Publication number
- ES2821821T3 ES2821821T3 ES15775688T ES15775688T ES2821821T3 ES 2821821 T3 ES2821821 T3 ES 2821821T3 ES 15775688 T ES15775688 T ES 15775688T ES 15775688 T ES15775688 T ES 15775688T ES 2821821 T3 ES2821821 T3 ES 2821821T3
- Authority
- ES
- Spain
- Prior art keywords
- methyl
- dihydroisoquinolin
- dichlorophenyl
- ethanone
- alkyl
- Prior art date
- 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.)
- Active
Links
- 125000003039 tetrahydroisoquinolinyl group Chemical class C1(NCCC2=CC=CC=C12)* 0.000 title 1
- -1 sulfonimidoyl Chemical group 0.000 claims abstract description 669
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 231
- 150000001875 compounds Chemical class 0.000 claims abstract description 164
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 132
- 239000001257 hydrogen Substances 0.000 claims abstract description 131
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 124
- 150000002367 halogens Chemical group 0.000 claims abstract description 123
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 97
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 77
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 63
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 60
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims abstract description 49
- 150000003839 salts Chemical class 0.000 claims abstract description 47
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 45
- 125000003368 amide group Chemical group 0.000 claims abstract description 32
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims abstract description 30
- 125000001424 substituent group Chemical group 0.000 claims abstract description 30
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 28
- 125000003118 aryl group Chemical group 0.000 claims abstract description 25
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 claims abstract description 24
- 125000005257 alkyl acyl group Chemical group 0.000 claims abstract description 24
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract description 22
- 125000003277 amino group Chemical group 0.000 claims abstract description 20
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 13
- 125000005281 alkyl ureido group Chemical group 0.000 claims abstract description 12
- 125000004043 oxo group Chemical group O=* 0.000 claims abstract description 11
- 125000001091 aminosulfinyl group Chemical group [H]N([H])S(*)=O 0.000 claims abstract description 10
- VLCPQJCYZTXACO-CYBMUJFWSA-N 2-(2-fluorophenyl)-1-[(1r)-1-methyl-3,4-dihydro-1h-isoquinolin-2-yl]ethanone Chemical compound N1([C@@H](C2=CC=CC=C2CC1)C)C(=O)CC1=CC=CC=C1F VLCPQJCYZTXACO-CYBMUJFWSA-N 0.000 claims abstract description 7
- 125000005195 alkyl amino carbonyloxy group Chemical group 0.000 claims abstract description 6
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 50
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 47
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims description 40
- 125000003545 alkoxy group Chemical group 0.000 claims description 40
- 208000010877 cognitive disease Diseases 0.000 claims description 21
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 17
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 15
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 14
- 239000000460 chlorine Substances 0.000 claims description 13
- 229910052801 chlorine Inorganic materials 0.000 claims description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- DPLHZOFCAIMEMK-LBPRGKRZSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(hydroxymethyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)CO)C DPLHZOFCAIMEMK-LBPRGKRZSA-N 0.000 claims description 12
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 12
- 208000028698 Cognitive impairment Diseases 0.000 claims description 11
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 11
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 208000027061 mild cognitive impairment Diseases 0.000 claims description 10
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims description 9
- NOXFPDLKIOZYRD-UEWDXFNNSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(1-hydroxyethyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(C)O)C NOXFPDLKIOZYRD-UEWDXFNNSA-N 0.000 claims description 9
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims description 9
- 239000008194 pharmaceutical composition Substances 0.000 claims description 9
- 238000002560 therapeutic procedure Methods 0.000 claims description 9
- XCMCCVHUFKZTSL-AWEZNQCLSA-N N-[2-[(1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]ethyl]methanesulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)CCNS(=O)(=O)C)C XCMCCVHUFKZTSL-AWEZNQCLSA-N 0.000 claims description 8
- 208000018737 Parkinson disease Diseases 0.000 claims description 8
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzenecarbonitrile Natural products N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 8
- QGYITPQJFPCDLU-LBPRGKRZSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinoline-5-carbonitrile Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C#N)C QGYITPQJFPCDLU-LBPRGKRZSA-N 0.000 claims description 7
- XZMCEPFQBRRENA-UHFFFAOYSA-N 2-(2,6-dichlorophenyl)-1-(4,4-difluoro-1-methyl-1,3-dihydroisoquinolin-2-yl)ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1C(C2=CC=CC=C2C(C1)(F)F)C XZMCEPFQBRRENA-UHFFFAOYSA-N 0.000 claims description 7
- DJDVRMKDRBYGFH-ZDUSSCGKSA-N N-[3-chloro-2-[2-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]phenyl]methanesulfonamide Chemical compound ClC=1C(=C(C=CC=1)NS(=O)(=O)C)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C DJDVRMKDRBYGFH-ZDUSSCGKSA-N 0.000 claims description 7
- DNIGFIYWEYFMPH-AWEZNQCLSA-N N-[[3-chloro-2-[2-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]phenyl]methyl]methanesulfonamide Chemical compound ClC=1C(=C(CNS(=O)(=O)C)C=CC=1)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C DNIGFIYWEYFMPH-AWEZNQCLSA-N 0.000 claims description 7
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims description 7
- YLMYMDDZTDMHJH-NSHDSACASA-N 1-[(1S)-5-amino-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-(2,6-dichlorophenyl)ethanone Chemical compound NC1=C2CCN([C@H](C2=CC=C1)C)C(CC1=C(C=CC=C1Cl)Cl)=O YLMYMDDZTDMHJH-NSHDSACASA-N 0.000 claims description 6
- SEZMJKDPBUXSKD-ZDUSSCGKSA-N N-[3-chloro-2-[2-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]phenyl]acetamide Chemical compound ClC=1C(=C(C=CC=1)NC(C)=O)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C SEZMJKDPBUXSKD-ZDUSSCGKSA-N 0.000 claims description 6
- IQFZDZTWJZTELA-AWEZNQCLSA-N N-[[3-chloro-2-[2-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]phenyl]methyl]acetamide Chemical compound ClC=1C(=C(CNC(C)=O)C=CC=1)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C IQFZDZTWJZTELA-AWEZNQCLSA-N 0.000 claims description 6
- 201000000980 schizophrenia Diseases 0.000 claims description 6
- UBWUVVWDCGFYPD-AWEZNQCLSA-N 1-[(1S)-5-(6-aminopyridin-3-yl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-(2,6-dichlorophenyl)ethanone Chemical compound NC1=CC=C(C=N1)C1=C2CCN([C@H](C2=CC=C1)C)C(CC1=C(C=CC=C1Cl)Cl)=O UBWUVVWDCGFYPD-AWEZNQCLSA-N 0.000 claims description 5
- ASLJDBYXXGCHTK-LBPRGKRZSA-N 2-(2,6-dichloro-3-methylsulfanylphenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1SC)Cl)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C ASLJDBYXXGCHTK-LBPRGKRZSA-N 0.000 claims description 5
- SUTPENAAFLOLOK-UHFFFAOYSA-N 2-(2,6-dichlorophenyl)-1-(1-methyl-3,4-dihydro-1H-isoquinolin-2-yl)ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1C(C2=CC=CC=C2CC1)C SUTPENAAFLOLOK-UHFFFAOYSA-N 0.000 claims description 5
- AFUYOGBIZRNGDR-AWEZNQCLSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-(1-methylsulfonyl-4,5-dihydroimidazol-2-yl)-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C=1N(CCN=1)S(=O)(=O)C)C AFUYOGBIZRNGDR-AWEZNQCLSA-N 0.000 claims description 5
- FEOHHTHXZNSXGV-ZDUSSCGKSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-(methylsulfanylmethyl)-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)CSC)C FEOHHTHXZNSXGV-ZDUSSCGKSA-N 0.000 claims description 5
- VBNNLDHIWIOGMO-LBPRGKRZSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-methylsulfonyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)C)C VBNNLDHIWIOGMO-LBPRGKRZSA-N 0.000 claims description 5
- LZMAIRDYFYWONZ-ZDUSSCGKSA-N 2-(2-chloro-6-methoxyphenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)OC)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C LZMAIRDYFYWONZ-ZDUSSCGKSA-N 0.000 claims description 5
- PVDDJNAOTDZFOR-LBPRGKRZSA-N 5-chloro-4-[2-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]pyridine-3-carbonitrile Chemical compound ClC=1C(=C(C=NC=1)C#N)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C PVDDJNAOTDZFOR-LBPRGKRZSA-N 0.000 claims description 5
- 208000024827 Alzheimer disease Diseases 0.000 claims description 5
- 206010002942 Apathy Diseases 0.000 claims description 5
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims description 5
- 208000023105 Huntington disease Diseases 0.000 claims description 5
- 208000009829 Lewy Body Disease Diseases 0.000 claims description 5
- 201000002832 Lewy body dementia Diseases 0.000 claims description 5
- 208000016285 Movement disease Diseases 0.000 claims description 5
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims description 5
- 125000005189 alkyl hydroxy group Chemical group 0.000 claims description 5
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 5
- 230000001149 cognitive effect Effects 0.000 claims description 5
- 206010013663 drug dependence Diseases 0.000 claims description 5
- 230000002265 prevention Effects 0.000 claims description 5
- 208000019116 sleep disease Diseases 0.000 claims description 5
- 208000011117 substance-related disease Diseases 0.000 claims description 5
- 208000024891 symptom Diseases 0.000 claims description 5
- OGJAIHIWVZHTBR-NSHDSACASA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-1,3-dihydroisoquinolin-4-one Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC=C2C(C1)=O)C OGJAIHIWVZHTBR-NSHDSACASA-N 0.000 claims description 4
- TXWXJJUQVRTLIH-ZDUSSCGKSA-N 1-[[(1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]methyl]-3-methylurea Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)CNC(=O)NC)C TXWXJJUQVRTLIH-ZDUSSCGKSA-N 0.000 claims description 4
- GAWZRMSXMKMAIC-UHFFFAOYSA-N 2-(2,6-dichlorophenyl)-1-(1,4,4-trimethyl-1,3-dihydroisoquinolin-2-yl)ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1C(C2=CC=CC=C2C(C1)(C)C)C GAWZRMSXMKMAIC-UHFFFAOYSA-N 0.000 claims description 4
- QSPAZLKGXQHBEQ-GTNSWQLSSA-N 2-(2,6-dichlorophenyl)-1-[(1S,4R)-4-hydroxy-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC=C2[C@H](C1)O)C QSPAZLKGXQHBEQ-GTNSWQLSSA-N 0.000 claims description 4
- UFEWTFQRSUQGSI-QFYYESIMSA-N 2-(3,5-dichloropyridin-4-yl)-1-[(1S,4R)-4-hydroxy-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC=1C=NC=C(C=1CC(=O)N1[C@H](C2=CC=CC=C2[C@H](C1)O)C)Cl UFEWTFQRSUQGSI-QFYYESIMSA-N 0.000 claims description 4
- QBQVRHDUTRBWDJ-NSHDSACASA-N 2-(3-bromo-2,6-dichlorophenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound BrC=1C(=C(C(=CC=1)Cl)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C)Cl QBQVRHDUTRBWDJ-NSHDSACASA-N 0.000 claims description 4
- NLWJAVIIJGNCTA-ZDUSSCGKSA-N 2-(3-chloro-5-methylpyridin-4-yl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC=1C=NC=C(C=1CC(=O)N1[C@H](C2=CC=CC=C2CC1)C)C NLWJAVIIJGNCTA-ZDUSSCGKSA-N 0.000 claims description 4
- PVIKUJDBAVWCCH-UHFFFAOYSA-N 2-[2,6-dichloro-4-(hydroxymethyl)phenyl]-1-(1-methyl-3,4-dihydro-1H-isoquinolin-2-yl)ethanone Chemical compound ClC1=C(C(=CC(=C1)CO)Cl)CC(=O)N1C(C2=CC=CC=C2CC1)C PVIKUJDBAVWCCH-UHFFFAOYSA-N 0.000 claims description 4
- IHWJRMOYVWXYJG-ZDUSSCGKSA-N 3-chloro-2-[2-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C IHWJRMOYVWXYJG-ZDUSSCGKSA-N 0.000 claims description 4
- WTEDLVUUFKFFHK-ZDUSSCGKSA-N 3-chloro-2-[2-[(1S)-1-methyl-5-methylsulfonyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)C)C WTEDLVUUFKFFHK-ZDUSSCGKSA-N 0.000 claims description 4
- QYJDNVVOIRSNCU-SGTLLEGYSA-N 3-chloro-2-[2-[(1S,4R)-4-hydroxy-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC=C2[C@H](C1)O)C QYJDNVVOIRSNCU-SGTLLEGYSA-N 0.000 claims description 4
- QYJDNVVOIRSNCU-KPZWWZAWSA-N 3-chloro-2-[2-[(1S,4S)-4-hydroxy-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC=C2[C@@H](C1)O)C QYJDNVVOIRSNCU-KPZWWZAWSA-N 0.000 claims description 4
- IEFSMNYTIJENAD-ZDUSSCGKSA-N N-[(1S)-2-[2-(2-chloro-6-cyanophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]methanesulfonamide Chemical compound ClC1=C(C(=CC=C1)C#N)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)NS(=O)(=O)C)C IEFSMNYTIJENAD-ZDUSSCGKSA-N 0.000 claims description 4
- ZGIVRTJLYCOXEN-AWEZNQCLSA-N N-[(1S)-2-[2-(2-chloro-6-methylphenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]methanesulfonamide Chemical compound ClC1=C(C(=CC=C1)C)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)NS(=O)(=O)C)C ZGIVRTJLYCOXEN-AWEZNQCLSA-N 0.000 claims description 4
- KLOIHOZALSMYAE-LBPRGKRZSA-N N-[2,4-dichloro-3-[2-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]phenyl]methanesulfonamide Chemical compound ClC1=C(C=CC(=C1CC(=O)N1[C@H](C2=CC=CC=C2CC1)C)Cl)NS(=O)(=O)C KLOIHOZALSMYAE-LBPRGKRZSA-N 0.000 claims description 4
- QOJIEXOWJGSHOR-UHFFFAOYSA-N N-[2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-7-yl]methanesulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1C(C2=CC(=CC=C2CC1)NS(=O)(=O)C)C QOJIEXOWJGSHOR-UHFFFAOYSA-N 0.000 claims description 4
- KXOWBRJAIKQBMP-ZDUSSCGKSA-N N-[[(1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]methyl]acetamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)CNC(C)=O)C KXOWBRJAIKQBMP-ZDUSSCGKSA-N 0.000 claims description 4
- MYTWVYBKMJPILA-ZDUSSCGKSA-N N-[[(1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]methyl]methanesulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)CNS(=O)(=O)C)C MYTWVYBKMJPILA-ZDUSSCGKSA-N 0.000 claims description 4
- MYTWVYBKMJPILA-UHFFFAOYSA-N N-[[2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]methyl]methanesulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1C(C2=CC=CC(=C2CC1)CNS(=O)(=O)C)C MYTWVYBKMJPILA-UHFFFAOYSA-N 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 239000003176 neuroleptic agent Substances 0.000 claims description 4
- QOSVHEYJMYRRHR-LBPRGKRZSA-N 2,4-dichloro-3-[2-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC1=C(C#N)C=CC(=C1CC(=O)N1[C@H](C2=CC=CC=C2CC1)C)Cl QOSVHEYJMYRRHR-LBPRGKRZSA-N 0.000 claims description 3
- SCNQMAWDBYZJGR-UNHBDAOFSA-N 2-(2,6-dichloro-3-methylsulfinylphenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1S(=O)C)Cl)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C SCNQMAWDBYZJGR-UNHBDAOFSA-N 0.000 claims description 3
- PTZTWTDGTUFDMO-LBPRGKRZSA-N 2-(2,6-dichloro-3-methylsulfonylphenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1S(=O)(=O)C)Cl)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C PTZTWTDGTUFDMO-LBPRGKRZSA-N 0.000 claims description 3
- FBPWXOHEFLFAAM-INIZCTEOSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-(2-methylpyridin-3-yl)-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C=1C(=NC=CC=1)C)C FBPWXOHEFLFAAM-INIZCTEOSA-N 0.000 claims description 3
- YVQHJIFZMQPQOS-LYKKTTPLSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-(2-methylpyrrolidine-1-carbonyl)-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(=O)N1C(CCC1)C)C YVQHJIFZMQPQOS-LYKKTTPLSA-N 0.000 claims description 3
- PXDSVCCYLZRAMK-JCYILVPMSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(2,5-dimethylpyrrolidine-1-carbonyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(=O)N1C(CCC1C)C)C PXDSVCCYLZRAMK-JCYILVPMSA-N 0.000 claims description 3
- PFNTZZIQUVJISH-AWEZNQCLSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(3,3-difluoropyrrolidine-1-carbonyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(=O)N1CC(CC1)(F)F)C PFNTZZIQUVJISH-AWEZNQCLSA-N 0.000 claims description 3
- HVRLTTNNEXNMRN-UHFFFAOYSA-N 2-(2,6-dichlorophenyl)-1-[5-(3,5-dimethyl-1,2-oxazol-4-yl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1C(C2=CC=CC(=C2CC1)C=1C(=NOC=1C)C)C HVRLTTNNEXNMRN-UHFFFAOYSA-N 0.000 claims description 3
- ZIDZNAHLMAQBRM-NSHDSACASA-N 2-(3,5-dichloropyridin-4-yl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC=1C=NC=C(C=1CC(=O)N1[C@H](C2=CC=CC=C2CC1)C)Cl ZIDZNAHLMAQBRM-NSHDSACASA-N 0.000 claims description 3
- JNBWVGWWYDYITI-NSHDSACASA-N 2-(3,5-dichloropyridin-4-yl)-1-[(1S)-1-methyl-5-methylsulfonyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC=1C=NC=C(C=1CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)C)C)Cl JNBWVGWWYDYITI-NSHDSACASA-N 0.000 claims description 3
- BMAJZCGKOCATRJ-LBPRGKRZSA-N 2-[2-chloro-6-(trifluoromethyl)phenyl]-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)C(F)(F)F)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C BMAJZCGKOCATRJ-LBPRGKRZSA-N 0.000 claims description 3
- FDJFAQRZXYRQKH-UHFFFAOYSA-N 2-chlorobenzonitrile 2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.ClC1=CC=CC=C1C#N FDJFAQRZXYRQKH-UHFFFAOYSA-N 0.000 claims description 3
- LKUBULRTNSPQHF-HNNXBMFYSA-N 3-chloro-2-[2-[(1S)-1-methyl-5-(1-methylpyrazol-4-yl)-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C=1C=NN(C=1)C)C LKUBULRTNSPQHF-HNNXBMFYSA-N 0.000 claims description 3
- PPAVDNOISOGVED-AWEZNQCLSA-N 3-chloro-2-[2-[(1S)-1-methyl-5-(1H-pyrazol-4-yl)-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C=1C=NNC=1)C PPAVDNOISOGVED-AWEZNQCLSA-N 0.000 claims description 3
- PJUCPHICQBSRFK-INIZCTEOSA-N 3-chloro-2-[2-[(1S)-1-methyl-5-pyridin-3-yl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C=1C=NC=CC=1)C PJUCPHICQBSRFK-INIZCTEOSA-N 0.000 claims description 3
- XTVJWXOAESOVGM-INIZCTEOSA-N 3-chloro-2-[2-[(1S)-1-methyl-5-pyridin-4-yl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C1=CC=NC=C1)C XTVJWXOAESOVGM-INIZCTEOSA-N 0.000 claims description 3
- JRMASVMQKUTZAX-HNNXBMFYSA-N 3-chloro-2-[2-[(1S)-5-(3,5-dimethyl-1,2-oxazol-4-yl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C=1C(=NOC=1C)C)C JRMASVMQKUTZAX-HNNXBMFYSA-N 0.000 claims description 3
- NDVSSADFNGSALM-INIZCTEOSA-N 3-chloro-2-[2-[(1S)-5-(3,5-dimethyl-1H-pyrazol-4-yl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C=1C(=NNC=1C)C)C NDVSSADFNGSALM-INIZCTEOSA-N 0.000 claims description 3
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- LFJQMFBGPGANMS-NSHDSACASA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinoline-5-sulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)S(=O)(=O)N)C LFJQMFBGPGANMS-NSHDSACASA-N 0.000 claims description 2
- WRGTTXFYNFHYGU-LBPRGKRZSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-N-(1H-1,2,4-triazol-5-yl)-3,4-dihydro-1H-isoquinoline-5-sulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)S(=O)(=O)NC1=NN=CN1)C WRGTTXFYNFHYGU-LBPRGKRZSA-N 0.000 claims description 2
- UJXVKMDZSPTBHW-LBPRGKRZSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-N-(2,2,2-trifluoroethyl)-3,4-dihydro-1H-isoquinoline-5-sulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)S(=O)(=O)NCC(F)(F)F)C UJXVKMDZSPTBHW-LBPRGKRZSA-N 0.000 claims description 2
- JGKLARRANXRQIR-AWEZNQCLSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-N-propan-2-yl-3,4-dihydro-1H-isoquinoline-5-sulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)S(=O)(=O)NC(C)C)C JGKLARRANXRQIR-AWEZNQCLSA-N 0.000 claims description 2
- KAPXIZGAXGHGPX-LBPRGKRZSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-N,1-dimethyl-3,4-dihydro-1H-isoquinoline-5-sulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)S(=O)(=O)NC)C KAPXIZGAXGHGPX-LBPRGKRZSA-N 0.000 claims description 2
- ATUSKDMTCNISHY-NGXIVSIZSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-N,N,1-trimethyl-3,4-dihydro-1H-isoquinoline-5-sulfinamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)S(=O)N(C)C)C ATUSKDMTCNISHY-NGXIVSIZSA-N 0.000 claims description 2
- BHEZRSYREDPXOA-ZDUSSCGKSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-N-ethyl-1-methyl-3,4-dihydro-1H-isoquinoline-5-sulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)S(=O)(=O)NCC)C BHEZRSYREDPXOA-ZDUSSCGKSA-N 0.000 claims description 2
- ODCVVYDDMMVPKU-LBPRGKRZSA-N 1-[(1S)-5-(2-amino-1,1-difluoroethyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-(2,6-dichlorophenyl)ethanone Chemical compound NCC(F)(F)C1=C2CCN([C@H](C2=CC=C1)C)C(CC1=C(C=CC=C1Cl)Cl)=O ODCVVYDDMMVPKU-LBPRGKRZSA-N 0.000 claims description 2
- LEQWSDJJUWAZLL-UNHBDAOFSA-N 2-(2,6-dichloro-4-methylsulfinylphenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC(=C1)S(=O)C)Cl)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C LEQWSDJJUWAZLL-UNHBDAOFSA-N 0.000 claims description 2
- CFNCYPFRVSGCJL-RSXQAXDFSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-4-methylsulfonyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC=C2C(C1)S(=O)(=O)C)C CFNCYPFRVSGCJL-RSXQAXDFSA-N 0.000 claims description 2
- SWQNGHPASLOVAR-LBPRGKRZSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-(2H-triazol-4-yl)-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C1=NNN=C1)C SWQNGHPASLOVAR-LBPRGKRZSA-N 0.000 claims description 2
- CPMBPUWIZFWXNZ-ZDUSSCGKSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-(methylsulfonylmethyl)-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)CS(=O)(=O)C)C CPMBPUWIZFWXNZ-ZDUSSCGKSA-N 0.000 claims description 2
- VKSUHOAKXKOXDP-HNNXBMFYSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-(morpholine-4-carbonyl)-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(=O)N1CCOCC1)C VKSUHOAKXKOXDP-HNNXBMFYSA-N 0.000 claims description 2
- GZEGZRPJFFORBG-INIZCTEOSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-(oxan-4-ylmethylsulfonyl)-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)CC1CCOCC1)C GZEGZRPJFFORBG-INIZCTEOSA-N 0.000 claims description 2
- XYSIMJUAGAQTAN-INIZCTEOSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-(pyridin-3-ylmethylsulfonyl)-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)CC=1C=NC=CC=1)C XYSIMJUAGAQTAN-INIZCTEOSA-N 0.000 claims description 2
- KAVCXHLEYQACFH-HNNXBMFYSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-(pyrrolidine-1-carbonyl)-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(=O)N1CCCC1)C KAVCXHLEYQACFH-HNNXBMFYSA-N 0.000 claims description 2
- SCYLEYZRTZGLGE-WLRWDXFRSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-[(1S)-2,2,2-trifluoro-1-hydroxyethyl]-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)[C@@H](C(F)(F)F)O)C SCYLEYZRTZGLGE-WLRWDXFRSA-N 0.000 claims description 2
- DGSDYFKMUVULTA-HNNXBMFYSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-[(5-methyl-1,2-oxazol-3-yl)methylsulfonyl]-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)CC1=NOC(=C1)C)C DGSDYFKMUVULTA-HNNXBMFYSA-N 0.000 claims description 2
- MWYJFWWXQVDBOI-VDBVYFBLSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-[(S)-methylsulfinyl]-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)[S@@](=O)C)C MWYJFWWXQVDBOI-VDBVYFBLSA-N 0.000 claims description 2
- MWYJFWWXQVDBOI-UNHBDAOFSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-methylsulfinyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound C[C@@H]1N(CCC2=C1C=CC=C2S(C)=O)C(=O)CC1=C(Cl)C=CC=C1Cl MWYJFWWXQVDBOI-UNHBDAOFSA-N 0.000 claims description 2
- JGDIVOCPXSSABP-AWEZNQCLSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-propan-2-ylsulfonyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)C(C)C)C JGDIVOCPXSSABP-AWEZNQCLSA-N 0.000 claims description 2
- AYCNHQPMNMXORF-HNNXBMFYSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-pyrrolidin-1-ylsulfonyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)N1CCCC1)C AYCNHQPMNMXORF-HNNXBMFYSA-N 0.000 claims description 2
- WNSOYBPPJVGOFN-LBPRGKRZSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(1,1-difluoro-2-hydroxyethyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(CO)(F)F)C WNSOYBPPJVGOFN-LBPRGKRZSA-N 0.000 claims description 2
- FZDGCNULRKUOLW-INIZCTEOSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(1,1-difluoro-2-morpholin-4-ylethyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(CN1CCOCC1)(F)F)C FZDGCNULRKUOLW-INIZCTEOSA-N 0.000 claims description 2
- PBBZAVCIGHGMRA-AWEZNQCLSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(3,3-difluoropyrrolidin-1-yl)sulfonyl-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)N1CC(CC1)(F)F)C PBBZAVCIGHGMRA-AWEZNQCLSA-N 0.000 claims description 2
- GCFVWELXXFWZSG-HNNXBMFYSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(3,5-dimethyl-1H-pyrazol-4-yl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C=1C(=NNC=1C)C)C GCFVWELXXFWZSG-HNNXBMFYSA-N 0.000 claims description 2
- UTVSMDMIJAHLDK-AWEZNQCLSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(3-hydroxypropyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)CCCO)C UTVSMDMIJAHLDK-AWEZNQCLSA-N 0.000 claims description 2
- FOTUCWKUQVKSQZ-NGXIVSIZSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(N,S-dimethylsulfonimidoyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=NC)C)C FOTUCWKUQVKSQZ-NGXIVSIZSA-N 0.000 claims description 2
- DYWZGNMAVPSQII-DCXKMBIZSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(N-ethyl-S-methylsulfonimidoyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=NCC)C)C DYWZGNMAVPSQII-DCXKMBIZSA-N 0.000 claims description 2
- RHNUMGCBWWLSAK-ZDUSSCGKSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(methoxymethylsulfonyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)COC)C RHNUMGCBWWLSAK-ZDUSSCGKSA-N 0.000 claims description 2
- SZPWNAAVXPXAHQ-GJZGRUSLSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-[(3S)-3-hydroxypyrrolidine-1-carbonyl]-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(=O)N1C[C@H](CC1)O)C SZPWNAAVXPXAHQ-GJZGRUSLSA-N 0.000 claims description 2
- QCGOYKWCLPXXPO-ZDUSSCGKSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-[1,1-difluoro-2-(methylamino)ethyl]-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(CNC)(F)F)C QCGOYKWCLPXXPO-ZDUSSCGKSA-N 0.000 claims description 2
- KJTOLQGGDJPVCE-ZDUSSCGKSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-ethylsulfonyl-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)CC)C KJTOLQGGDJPVCE-ZDUSSCGKSA-N 0.000 claims description 2
- MVYAHFYNYPHPEM-NSHDSACASA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-hydroxy-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)O)C MVYAHFYNYPHPEM-NSHDSACASA-N 0.000 claims description 2
- QUYRYOXULZRZSQ-SGTLLEGYSA-N 2-(2,6-dichlorophenyl)-1-[(1S,4R)-4-methoxy-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC=C2[C@H](C1)OC)C QUYRYOXULZRZSQ-SGTLLEGYSA-N 0.000 claims description 2
- QSPAZLKGXQHBEQ-APPDUMDISA-N 2-(2,6-dichlorophenyl)-1-[(1S,4S)-4-hydroxy-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC=C2[C@@H](C1)O)C QSPAZLKGXQHBEQ-APPDUMDISA-N 0.000 claims description 2
- QUYRYOXULZRZSQ-KPZWWZAWSA-N 2-(2,6-dichlorophenyl)-1-[(1S,4S)-4-methoxy-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC=C2[C@@H](C1)OC)C QUYRYOXULZRZSQ-KPZWWZAWSA-N 0.000 claims description 2
- HZRJBMRCAHZXOW-ZDUSSCGKSA-N 2-(2-chloro-6-methylsulfanylphenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)SC)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C HZRJBMRCAHZXOW-ZDUSSCGKSA-N 0.000 claims description 2
- PWPVXQSWLIJMPU-LNHXHEARSA-N 2-(2-chloro-6-methylsulfinylphenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound C[C@@H]1N(CCC2=C1C=CC=C2)C(=O)CC1=C(Cl)C=CC=C1S(C)=O PWPVXQSWLIJMPU-LNHXHEARSA-N 0.000 claims description 2
- KAYRYAJECIEJHR-ZDUSSCGKSA-N 2-(2-chloro-6-methylsulfonylphenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound C[C@@H]1N(CCC2=C1C=CC=C2)C(=O)CC1=C(Cl)C=CC=C1S(C)(=O)=O KAYRYAJECIEJHR-ZDUSSCGKSA-N 0.000 claims description 2
- ZGWQBQQCISAIDW-NSHDSACASA-N 2-(3,5-dichloro-2-methoxypyridin-4-yl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC=1C(=NC=C(C=1CC(=O)N1[C@H](C2=CC=CC=C2CC1)C)Cl)OC ZGWQBQQCISAIDW-NSHDSACASA-N 0.000 claims description 2
- WTAUFGSBTGSXFK-YPMLDQLKSA-N 2-(3,5-dichloropyridin-4-yl)-1-[(1S)-1-methyl-5-[(1S)-2,2,2-trifluoro-1-hydroxyethyl]-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC=1C=NC=C(C=1CC(=O)N1[C@H](C2=CC=CC(=C2CC1)[C@@H](C(F)(F)F)O)C)Cl WTAUFGSBTGSXFK-YPMLDQLKSA-N 0.000 claims description 2
- AYOOQYTVFQAVDM-NSHDSACASA-N 2-(3,5-dichloropyridin-4-yl)-1-[(1S)-5-(hydroxymethyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC=1C=NC=C(C=1CC(=O)N1[C@H](C2=CC=CC(=C2CC1)CO)C)Cl AYOOQYTVFQAVDM-NSHDSACASA-N 0.000 claims description 2
- UOIJYYJIKGKMLE-QKVFXAPYSA-N 2-(5-chloro-1H-indol-4-yl)-1-[(1S)-1-methyl-5-[(1S)-2,2,2-trifluoro-1-hydroxyethyl]-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC=1C(=C2C=CNC2=CC=1)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)[C@@H](C(F)(F)F)O)C UOIJYYJIKGKMLE-QKVFXAPYSA-N 0.000 claims description 2
- RIIZCSYXYIHVNK-LBPRGKRZSA-N 2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC=1C(=C2C(=NC=1)NC=C2)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C RIIZCSYXYIHVNK-LBPRGKRZSA-N 0.000 claims description 2
- GDYSUYMONIMNBB-NSHDSACASA-N 2-[(1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]-2,2-difluoroacetamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(C(=O)N)(F)F)C GDYSUYMONIMNBB-NSHDSACASA-N 0.000 claims description 2
- GCXKWDABQWNELY-LBPRGKRZSA-N 2-[2,6-dichloro-3-(hydroxymethyl)phenyl]-1-[(1S)-1-methyl-5-methylsulfonyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1CO)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)C)C GCXKWDABQWNELY-LBPRGKRZSA-N 0.000 claims description 2
- DNEXEDCVTLMTOH-ZDUSSCGKSA-N 2-[2-chloro-6-(hydroxymethyl)phenyl]-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)CO)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C DNEXEDCVTLMTOH-ZDUSSCGKSA-N 0.000 claims description 2
- VEICFIKQSUFLLL-AWEZNQCLSA-N 2-[2-chloro-6-(methylsulfonylmethyl)phenyl]-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)CS(=O)(=O)C)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C VEICFIKQSUFLLL-AWEZNQCLSA-N 0.000 claims description 2
- UQMJQPDEDGRSRW-JTQLQIEISA-N 3,5-dichloro-4-[2-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]-1H-pyridin-2-one Chemical compound ClC=1C(NC=C(C=1CC(=O)N1[C@H](C2=CC=CC=C2CC1)C)Cl)=O UQMJQPDEDGRSRW-JTQLQIEISA-N 0.000 claims description 2
- DBJKODBKVNXIDA-YUNKPMOVSA-N 3-chloro-2-[2-[(1S)-1-methyl-5-[(1S)-2,2,2-trifluoro-1-hydroxyethyl]-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound C[C@@H]1N(CCC2=C1C=CC=C2[C@H](O)C(F)(F)F)C(=O)CC1=C(C=CC=C1Cl)C#N DBJKODBKVNXIDA-YUNKPMOVSA-N 0.000 claims description 2
- HCSANWUAUOUNMC-ZDUSSCGKSA-N 3-chloro-2-[2-[(1S)-1-methyl-5-[5-(trifluoromethyl)-1H-pyrazol-4-yl]-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C=1C(=NNC=1)C(F)(F)F)C HCSANWUAUOUNMC-ZDUSSCGKSA-N 0.000 claims description 2
- OUZHRNRLBJNLDA-INIZCTEOSA-N 3-chloro-2-[2-[(1S)-1-methyl-5-pyridin-2-yl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound ClC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C1=NC=CC=C1)C OUZHRNRLBJNLDA-INIZCTEOSA-N 0.000 claims description 2
- IVLFCHTXVGNPJW-AWEZNQCLSA-N 3-methoxy-2-[2-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzonitrile Chemical compound COC=1C(=C(C#N)C=CC=1)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C IVLFCHTXVGNPJW-AWEZNQCLSA-N 0.000 claims description 2
- SCCQNOIYGRUXTH-AWEZNQCLSA-N 4-[(1S)-2-[2-(2-chloro-6-cyanophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]-1H-pyrazole-5-carbonitrile Chemical compound ClC1=C(C(=CC=C1)C#N)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C=1C(=NNC=1)C#N)C SCCQNOIYGRUXTH-AWEZNQCLSA-N 0.000 claims description 2
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 2
- ZNDJCSCCKDYWSU-SZQRVLIRSA-N 6-[(1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]morpholin-3-one Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C1OCC(NC1)=O)C ZNDJCSCCKDYWSU-SZQRVLIRSA-N 0.000 claims description 2
- IPNHPNIATOHDNN-LBPRGKRZSA-N N-[(1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]methanesulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)NS(=O)(=O)C)C IPNHPNIATOHDNN-LBPRGKRZSA-N 0.000 claims description 2
- JGHZNARWTIMBRF-ZDUSSCGKSA-N N-[2-[(1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]-2,2-difluoroethyl]acetamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(CNC(C)=O)(F)F)C JGHZNARWTIMBRF-ZDUSSCGKSA-N 0.000 claims description 2
- LYRBTLUUZQMSTC-KPZWWZAWSA-N [(1S,4S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-4-yl] N-methylcarbamate Chemical compound CNC(O[C@@H]1CN([C@H](C2=CC=CC=C12)C)C(CC1=C(C=CC=C1Cl)Cl)=O)=O LYRBTLUUZQMSTC-KPZWWZAWSA-N 0.000 claims description 2
- 208000022925 sleep disturbance Diseases 0.000 claims description 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 3
- SVPHHUOSSDYMME-RSAXXLAASA-N 2-[2-[(1S)-5-(2-aminopyridin-4-yl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]-3-chlorobenzonitrile 2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.C[C@@H]1N(CCc2c1cccc2-c1ccnc(N)c1)C(=O)Cc1c(Cl)cccc1C#N SVPHHUOSSDYMME-RSAXXLAASA-N 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract description 23
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract description 15
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract description 11
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract description 6
- 239000000243 solution Substances 0.000 description 217
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 211
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 200
- 230000015572 biosynthetic process Effects 0.000 description 187
- 238000003786 synthesis reaction Methods 0.000 description 187
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 181
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 177
- 239000011541 reaction mixture Substances 0.000 description 141
- 239000000203 mixture Substances 0.000 description 131
- 235000019439 ethyl acetate Nutrition 0.000 description 89
- 239000012044 organic layer Substances 0.000 description 84
- 238000000034 method Methods 0.000 description 80
- 239000007787 solid Substances 0.000 description 80
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 79
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 76
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 66
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 64
- 239000003480 eluent Substances 0.000 description 64
- 150000002431 hydrogen Chemical group 0.000 description 63
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 63
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 60
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 59
- 239000000543 intermediate Substances 0.000 description 58
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 54
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 53
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 52
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 51
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 49
- 238000004366 reverse phase liquid chromatography Methods 0.000 description 49
- 229910052938 sodium sulfate Inorganic materials 0.000 description 49
- 235000011152 sodium sulphate Nutrition 0.000 description 49
- 239000007832 Na2SO4 Substances 0.000 description 48
- 238000005160 1H NMR spectroscopy Methods 0.000 description 47
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 46
- 229920006395 saturated elastomer Polymers 0.000 description 44
- 238000000746 purification Methods 0.000 description 41
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 39
- 238000004440 column chromatography Methods 0.000 description 37
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 33
- 235000019341 magnesium sulphate Nutrition 0.000 description 33
- 239000002904 solvent Substances 0.000 description 31
- 235000017557 sodium bicarbonate Nutrition 0.000 description 30
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 30
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 29
- 239000003921 oil Substances 0.000 description 29
- 235000019198 oils Nutrition 0.000 description 29
- 238000006243 chemical reaction Methods 0.000 description 25
- 239000002253 acid Substances 0.000 description 24
- 238000004458 analytical method Methods 0.000 description 24
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 23
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 20
- 239000012267 brine Substances 0.000 description 19
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 18
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 18
- 229910052794 bromium Inorganic materials 0.000 description 18
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 17
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 16
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 16
- 238000010828 elution Methods 0.000 description 16
- 125000001153 fluoro group Chemical group F* 0.000 description 16
- 238000004128 high performance liquid chromatography Methods 0.000 description 16
- 102000005962 receptors Human genes 0.000 description 16
- 108020003175 receptors Proteins 0.000 description 16
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 15
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 15
- 239000002585 base Substances 0.000 description 15
- 125000001425 triazolyl group Chemical group 0.000 description 15
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 14
- 235000011114 ammonium hydroxide Nutrition 0.000 description 14
- 239000000706 filtrate Substances 0.000 description 14
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 description 14
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 14
- 125000004076 pyridyl group Chemical group 0.000 description 14
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 description 13
- 229910052717 sulfur Inorganic materials 0.000 description 13
- 150000003526 tetrahydroisoquinolines Chemical class 0.000 description 13
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 12
- IYQQKMMPEFAUDG-LBPRGKRZSA-N 1-[(1S)-5-(aminomethyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-(2,6-dichlorophenyl)ethanone Chemical compound NCC1=C2CCN([C@H](C2=CC=C1)C)C(CC1=C(C=CC=C1Cl)Cl)=O IYQQKMMPEFAUDG-LBPRGKRZSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 230000002378 acidificating effect Effects 0.000 description 12
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 11
- WINHDLXZRUUNAW-UHFFFAOYSA-N 3-chloro-5-methyl-4-prop-2-enylpyridine Chemical compound ClC=1C=NC=C(C=1CC=C)C WINHDLXZRUUNAW-UHFFFAOYSA-N 0.000 description 11
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 11
- 125000002757 morpholinyl group Chemical group 0.000 description 11
- 238000000926 separation method Methods 0.000 description 11
- 239000007858 starting material Substances 0.000 description 11
- VPKHWEFDYAMWOS-UHFFFAOYSA-N 5-bromo-1-methyl-1,2,3,4-tetrahydroisoquinoline Chemical compound C1=CC=C2C(C)NCCC2=C1Br VPKHWEFDYAMWOS-UHFFFAOYSA-N 0.000 description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 10
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 10
- 229910052786 argon Inorganic materials 0.000 description 10
- 230000008878 coupling Effects 0.000 description 10
- 238000010168 coupling process Methods 0.000 description 10
- 238000005859 coupling reaction Methods 0.000 description 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 10
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 10
- 239000002798 polar solvent Substances 0.000 description 10
- 239000012279 sodium borohydride Substances 0.000 description 10
- 229910000033 sodium borohydride Inorganic materials 0.000 description 10
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 10
- 239000003643 water by type Substances 0.000 description 10
- CYPYTURSJDMMMP-WVCUSYJESA-N (1e,4e)-1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 CYPYTURSJDMMMP-WVCUSYJESA-N 0.000 description 9
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 9
- 150000001412 amines Chemical class 0.000 description 9
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 9
- 239000010410 layer Substances 0.000 description 9
- HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 description 9
- 238000004808 supercritical fluid chromatography Methods 0.000 description 9
- JNEBEMFPZPRRCB-LBPRGKRZSA-N 2-(2-chloro-6-iodophenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)I)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C JNEBEMFPZPRRCB-LBPRGKRZSA-N 0.000 description 8
- JJTWHDHLYIONDV-UHFFFAOYSA-N 2-(3-bromo-2,6-dichlorophenyl)acetic acid Chemical compound OC(=O)CC1=C(Cl)C=CC(Br)=C1Cl JJTWHDHLYIONDV-UHFFFAOYSA-N 0.000 description 8
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 8
- 239000012359 Methanesulfonyl chloride Substances 0.000 description 8
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 125000005843 halogen group Chemical group 0.000 description 8
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 8
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 8
- GTCAXTIRRLKXRU-UHFFFAOYSA-N methyl carbamate Chemical compound COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 8
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- GQLDKRHWSODCHU-BYDSUWOYSA-N (1S)-1-methyl-1,2,3,4-tetrahydroisoquinolin-4-ol Chemical compound C[C@@H]1NCC(C2=CC=CC=C12)O GQLDKRHWSODCHU-BYDSUWOYSA-N 0.000 description 7
- GEWSBHFZERUDJC-ZDUSSCGKSA-N (1S)-1-methyl-2-(4-methylphenyl)sulfonyl-1,3-dihydroisoquinolin-4-one Chemical compound C[C@@H]1N(CC(C2=CC=CC=C12)=O)S(=O)(=O)C1=CC=C(C=C1)C GEWSBHFZERUDJC-ZDUSSCGKSA-N 0.000 description 7
- ZGPVDSQEKCBAHW-LBPRGKRZSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinoline-5-carbaldehyde Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C=O)C ZGPVDSQEKCBAHW-LBPRGKRZSA-N 0.000 description 7
- FOGKWBRULVDKFN-LBPRGKRZSA-N 2-(2-amino-6-chlorophenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound NC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C FOGKWBRULVDKFN-LBPRGKRZSA-N 0.000 description 7
- ACXGOCPMJWHJBW-ZDUSSCGKSA-N 2-[2-(aminomethyl)-6-chlorophenyl]-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound NCC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C ACXGOCPMJWHJBW-ZDUSSCGKSA-N 0.000 description 7
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical class OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 7
- 239000003153 chemical reaction reagent Substances 0.000 description 7
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 7
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- WCBHPCZVWBWNDO-HKALDPMFSA-N tert-butyl (1S)-1-methyl-5-(5-oxomorpholin-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical class C[C@@H]1N(CCC2=C(C=CC=C12)C1CNC(CO1)=O)C(=O)OC(C)(C)C WCBHPCZVWBWNDO-HKALDPMFSA-N 0.000 description 7
- YPWQQEYFVLOTDF-ZDUSSCGKSA-N tert-butyl (1S)-5-(3-methoxy-3-oxopropyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound COC(CCC1=C2CCN([C@H](C2=CC=C1)C)C(=O)OC(C)(C)C)=O YPWQQEYFVLOTDF-ZDUSSCGKSA-N 0.000 description 7
- PPAKSFPSRMJQQH-CWQZNGJJSA-N (1S)-1-methyl-2-(4-methylphenyl)sulfonyl-3,4-dihydro-1H-isoquinolin-4-ol Chemical compound C[C@@H]1N(CC(C2=CC=CC=C12)O)S(=O)(=O)C1=CC=C(C=C1)C PPAKSFPSRMJQQH-CWQZNGJJSA-N 0.000 description 6
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 description 6
- KZPYGQFFRCFCPP-UHFFFAOYSA-N 1,1'-bis(diphenylphosphino)ferrocene Chemical compound [Fe+2].C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1 KZPYGQFFRCFCPP-UHFFFAOYSA-N 0.000 description 6
- ZHHMZEVJHMYDAQ-UHFFFAOYSA-N 1,3-dichloro-5-fluoro-2-prop-2-enylbenzene Chemical compound ClC1=C(C(=CC(=C1)F)Cl)CC=C ZHHMZEVJHMYDAQ-UHFFFAOYSA-N 0.000 description 6
- IXFDFHBVHBVZBR-UHFFFAOYSA-N 1-(benzenesulfonyl)-4-nitroindole Chemical compound C1=CC=2C([N+](=O)[O-])=CC=CC=2N1S(=O)(=O)C1=CC=CC=C1 IXFDFHBVHBVZBR-UHFFFAOYSA-N 0.000 description 6
- WQIVMFVWMSQAGS-ZDUSSCGKSA-N 1-[(1S)-5-(2-aminoethyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-(2,6-dichlorophenyl)ethanone Chemical compound NCCC1=C2CCN([C@H](C2=CC=C1)C)C(CC1=C(C=CC=C1Cl)Cl)=O WQIVMFVWMSQAGS-ZDUSSCGKSA-N 0.000 description 6
- QGPXACAMXUUPAV-LBPRGKRZSA-N 1-[(1S)-5-(bromomethyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-(2,6-dichlorophenyl)ethanone Chemical compound BrCC1=C2CCN([C@H](C2=CC=C1)C)C(CC1=C(C=CC=C1Cl)Cl)=O QGPXACAMXUUPAV-LBPRGKRZSA-N 0.000 description 6
- UOBLQIKFQVPGRA-NSHDSACASA-N 1-[(1S)-5-bromo-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-(2,6-dichlorophenyl)ethanone Chemical compound BrC1=C2CCN([C@H](C2=CC=C1)C)C(CC1=C(C=CC=C1Cl)Cl)=O UOBLQIKFQVPGRA-NSHDSACASA-N 0.000 description 6
- JZNQNKXUCYQJIT-UHFFFAOYSA-N 2-(2,6-dichloro-3-methoxycarbonylphenyl)acetic acid Chemical compound ClC1=C(C(=CC=C1C(=O)OC)Cl)CC(=O)O JZNQNKXUCYQJIT-UHFFFAOYSA-N 0.000 description 6
- SRPCVDHPFLWYGX-UHFFFAOYSA-N 2-(3,5-dichloro-2-methoxypyridin-4-yl)acetonitrile Chemical compound ClC=1C(=NC=C(C=1CC#N)Cl)OC SRPCVDHPFLWYGX-UHFFFAOYSA-N 0.000 description 6
- DSPHLEATCTXQIE-UHFFFAOYSA-N 2-(3-carbamoyl-2,6-dichlorophenyl)acetic acid Chemical compound C(N)(=O)C=1C(=C(C(=CC=1)Cl)CC(=O)O)Cl DSPHLEATCTXQIE-UHFFFAOYSA-N 0.000 description 6
- TWYTUWGQFSBBRA-UHFFFAOYSA-N 2-(4-bromo-2,6-dichlorophenyl)acetic acid Chemical compound OC(=O)CC1=C(Cl)C=C(Br)C=C1Cl TWYTUWGQFSBBRA-UHFFFAOYSA-N 0.000 description 6
- WUTKJZGYMPMUSI-UHFFFAOYSA-N 5-bromo-1-methyl-3,4-dihydroisoquinoline Chemical compound C1=CC=C2C(C)=NCCC2=C1Br WUTKJZGYMPMUSI-UHFFFAOYSA-N 0.000 description 6
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 6
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 6
- 238000005481 NMR spectroscopy Methods 0.000 description 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 6
- 230000003281 allosteric effect Effects 0.000 description 6
- 235000019270 ammonium chloride Nutrition 0.000 description 6
- 238000004807 desolvation Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
- 229940062627 tribasic potassium phosphate Drugs 0.000 description 6
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 6
- YBILZOWIRBPGHP-NSHDSACASA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinoline-5-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C(=O)N)C YBILZOWIRBPGHP-NSHDSACASA-N 0.000 description 5
- SSJXIUAHEKJCMH-PHDIDXHHSA-N (1r,2r)-cyclohexane-1,2-diamine Chemical compound N[C@@H]1CCCC[C@H]1N SSJXIUAHEKJCMH-PHDIDXHHSA-N 0.000 description 5
- QPILYVQSKNWRDD-QMMMGPOBSA-N (1s)-1-methyl-1,2,3,4-tetrahydroisoquinoline Chemical compound C1=CC=C2[C@H](C)NCCC2=C1 QPILYVQSKNWRDD-QMMMGPOBSA-N 0.000 description 5
- XCYSPHKJYNXUOD-UHFFFAOYSA-N 1-(7-bromo-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl)-2-(2,6-dichlorophenyl)ethanone Chemical compound BrC1=CC=C2CCN(C(C2=C1)C)C(CC1=C(C=CC=C1Cl)Cl)=O XCYSPHKJYNXUOD-UHFFFAOYSA-N 0.000 description 5
- UDNDMXOPGYGUHZ-UHFFFAOYSA-N 1-(benzenesulfonyl)-5-chloro-4-iodoindole Chemical compound C1(=CC=CC=C1)S(=O)(=O)N1C=CC2=C(C(=CC=C12)Cl)I UDNDMXOPGYGUHZ-UHFFFAOYSA-N 0.000 description 5
- LFSBOZGFABXBBK-UHFFFAOYSA-N 1-(benzenesulfonyl)-5-chloroindol-4-amine Chemical compound C1(=CC=CC=C1)S(=O)(=O)N1C=CC=2C(=C(C=CC1=2)Cl)N LFSBOZGFABXBBK-UHFFFAOYSA-N 0.000 description 5
- XQPCIFQSPLEMHI-UHFFFAOYSA-N 1-(benzenesulfonyl)indol-4-amine Chemical compound C1=CC=2C(N)=CC=CC=2N1S(=O)(=O)C1=CC=CC=C1 XQPCIFQSPLEMHI-UHFFFAOYSA-N 0.000 description 5
- XNFIMPKPIYVBEH-UHFFFAOYSA-N 2-(2,6-dichloro-3-cyanophenyl)acetic acid Chemical compound ClC1=C(C(=CC=C1C#N)Cl)CC(=O)O XNFIMPKPIYVBEH-UHFFFAOYSA-N 0.000 description 5
- HTKOICGALGBAIQ-UHFFFAOYSA-N 2-(2,6-dichloro-4-cyanophenyl)acetic acid Chemical compound ClC1=C(C(=CC(=C1)C#N)Cl)CC(=O)O HTKOICGALGBAIQ-UHFFFAOYSA-N 0.000 description 5
- MIDHYPREMXHZFD-LBPRGKRZSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-methylsulfanyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)SC)C MIDHYPREMXHZFD-LBPRGKRZSA-N 0.000 description 5
- SFAILOOQFZNOAU-UHFFFAOYSA-N 2-(2,6-dichlorophenyl)acetic acid Chemical compound OC(=O)CC1=C(Cl)C=CC=C1Cl SFAILOOQFZNOAU-UHFFFAOYSA-N 0.000 description 5
- LOWMXVMCPLJTPQ-UHFFFAOYSA-N 2-(2-bromo-6-methoxyphenyl)acetic acid Chemical compound COC1=CC=CC(Br)=C1CC(O)=O LOWMXVMCPLJTPQ-UHFFFAOYSA-N 0.000 description 5
- JJXRIEDGRJPKLP-UHFFFAOYSA-N 2-(2-bromo-6-methoxyphenyl)acetonitrile Chemical compound COC1=CC=CC(Br)=C1CC#N JJXRIEDGRJPKLP-UHFFFAOYSA-N 0.000 description 5
- UJRQVBVGNAXYCU-UHFFFAOYSA-N 2-(3,5-dichloro-2-methoxypyridin-4-yl)acetic acid Chemical compound ClC=1C(=NC=C(C=1CC(=O)O)Cl)OC UJRQVBVGNAXYCU-UHFFFAOYSA-N 0.000 description 5
- ILWZCMSVKPZKJT-UHFFFAOYSA-N 2-(3-bromo-2,6-dichlorophenyl)acetonitrile Chemical compound BrC=1C(=C(C(=CC=1)Cl)CC#N)Cl ILWZCMSVKPZKJT-UHFFFAOYSA-N 0.000 description 5
- VTVNWMIIEZTUGW-UHFFFAOYSA-N 2-(3-chloro-5-methylpyridin-4-yl)acetic acid Chemical compound CC1=CN=CC(Cl)=C1CC(O)=O VTVNWMIIEZTUGW-UHFFFAOYSA-N 0.000 description 5
- DYDORDQBILMKCL-UHFFFAOYSA-N 2-(5-chloro-1H-indazol-4-yl)acetic acid Chemical compound ClC=1C(=C2C=NNC2=CC=1)CC(=O)O DYDORDQBILMKCL-UHFFFAOYSA-N 0.000 description 5
- RCEPBBDOEJRFTA-UHFFFAOYSA-N 2-(5-chloro-1H-indol-4-yl)acetic acid Chemical compound ClC=1C(=C2C=CNC2=CC=1)CC(=O)O RCEPBBDOEJRFTA-UHFFFAOYSA-N 0.000 description 5
- PQPQLYSVDIADRY-UHFFFAOYSA-N 2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)acetic acid Chemical compound ClC=1C(=C2C(=NC=1)NC=C2)CC(=O)O PQPQLYSVDIADRY-UHFFFAOYSA-N 0.000 description 5
- WVAUWEMOURERDF-UHFFFAOYSA-N 3,5-dichloro-4-iodo-2-methoxypyridine Chemical compound ClC=1C(=NC=C(C=1I)Cl)OC WVAUWEMOURERDF-UHFFFAOYSA-N 0.000 description 5
- VARLYOBBIWKREP-UHFFFAOYSA-N 3-chloro-4-iodo-5-methylpyridine Chemical compound ClC=1C=NC=C(C=1I)C VARLYOBBIWKREP-UHFFFAOYSA-N 0.000 description 5
- WINZSCFBQMKAFJ-UHFFFAOYSA-N 4,4-difluoro-1-methyl-2,3-dihydro-1H-isoquinoline Chemical compound FC1(CNC(C2=CC=CC=C12)C)F WINZSCFBQMKAFJ-UHFFFAOYSA-N 0.000 description 5
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 5
- ODWZSTIFGXNASR-UHFFFAOYSA-N 5-chloro-4-iodo-1-(oxan-2-yl)indazole Chemical compound ClC=1C(=C2C=NN(C2=CC=1)C1OCCCC1)I ODWZSTIFGXNASR-UHFFFAOYSA-N 0.000 description 5
- WKXOECKPJPOIBK-UHFFFAOYSA-N 7-bromo-1-methyl-3,4-dihydroisoquinoline Chemical compound C1=C(Br)C=C2C(C)=NCCC2=C1 WKXOECKPJPOIBK-UHFFFAOYSA-N 0.000 description 5
- IEDMTCUEHMCUJW-UHFFFAOYSA-N 7-bromo-10b-methyl-5,6-dihydro-[1,3]oxazolo[2,3-a]isoquinoline-2,3-dione Chemical compound BrC1=C2CCN3C(C2=CC=C1)(OC(C3=O)=O)C IEDMTCUEHMCUJW-UHFFFAOYSA-N 0.000 description 5
- WZRPCODOMYHSND-UHFFFAOYSA-N 9-bromo-10b-methyl-5,6-dihydro-[1,3]oxazolo[2,3-a]isoquinoline-2,3-dione Chemical compound BrC1=CC=C2CCN3C(C2=C1)(OC(C3=O)=O)C WZRPCODOMYHSND-UHFFFAOYSA-N 0.000 description 5
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 5
- 102000003688 G-Protein-Coupled Receptors Human genes 0.000 description 5
- 108090000045 G-Protein-Coupled Receptors Proteins 0.000 description 5
- UCXLLHMIJPLMSQ-QRPNPIFTSA-N [(1S)-1-methyl-1,2,3,4-tetrahydroisoquinolin-5-yl]methanol hydrochloride Chemical compound Cl.C[C@@H]1NCCc2c(CO)cccc12 UCXLLHMIJPLMSQ-QRPNPIFTSA-N 0.000 description 5
- GPDHNZNLPKYHCN-DZOOLQPHSA-N [[(z)-(1-cyano-2-ethoxy-2-oxoethylidene)amino]oxy-morpholin-4-ylmethylidene]-dimethylazanium;hexafluorophosphate Chemical compound F[P-](F)(F)(F)(F)F.CCOC(=O)C(\C#N)=N/OC(=[N+](C)C)N1CCOCC1 GPDHNZNLPKYHCN-DZOOLQPHSA-N 0.000 description 5
- 239000013543 active substance Substances 0.000 description 5
- 239000000556 agonist Substances 0.000 description 5
- VZTDIZULWFCMLS-UHFFFAOYSA-N ammonium formate Chemical compound [NH4+].[O-]C=O VZTDIZULWFCMLS-UHFFFAOYSA-N 0.000 description 5
- CBHOOMGKXCMKIR-UHFFFAOYSA-N azane;methanol Chemical compound N.OC CBHOOMGKXCMKIR-UHFFFAOYSA-N 0.000 description 5
- MCQRPQCQMGVWIQ-UHFFFAOYSA-N boron;methylsulfanylmethane Chemical compound [B].CSC MCQRPQCQMGVWIQ-UHFFFAOYSA-N 0.000 description 5
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 229960003638 dopamine Drugs 0.000 description 5
- 239000011630 iodine Substances 0.000 description 5
- 229910052740 iodine Inorganic materials 0.000 description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
- 125000002971 oxazolyl group Chemical group 0.000 description 5
- 238000005191 phase separation Methods 0.000 description 5
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 5
- YHJIGQIWLFZKQN-UHFFFAOYSA-N tert-butyl 5-bromo-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound BrC1=C2CCN(C(C2=CC=C1)C)C(=O)OC(C)(C)C YHJIGQIWLFZKQN-UHFFFAOYSA-N 0.000 description 5
- 229910052721 tungsten Inorganic materials 0.000 description 5
- GTLDTDOJJJZVBW-UHFFFAOYSA-N zinc cyanide Chemical compound [Zn+2].N#[C-].N#[C-] GTLDTDOJJJZVBW-UHFFFAOYSA-N 0.000 description 5
- FXTPEWOXDMOOFW-NSHDSACASA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinoline-5-carboxylic acid Chemical compound C[C@@H]1N(CCC2=C1C=CC=C2C(O)=O)C(=O)CC1=C(Cl)C=CC=C1Cl FXTPEWOXDMOOFW-NSHDSACASA-N 0.000 description 4
- IPYYTLYWQXCNKF-UHFFFAOYSA-N (5-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)methanol Chemical compound ClC=1C(=C2C(=NC=1)NC=C2)CO IPYYTLYWQXCNKF-UHFFFAOYSA-N 0.000 description 4
- PYYJGBRXHSGOBY-UHFFFAOYSA-N 2-(2,6-dichloro-4-fluorophenyl)acetic acid Chemical compound ClC1=C(C(=CC(=C1)F)Cl)CC(=O)O PYYJGBRXHSGOBY-UHFFFAOYSA-N 0.000 description 4
- HVUHKUNGQXCSGG-UHFFFAOYSA-N 2-(4-bromo-2,6-dichlorophenyl)acetonitrile Chemical compound BrC1=CC(=C(C(=C1)Cl)CC#N)Cl HVUHKUNGQXCSGG-UHFFFAOYSA-N 0.000 description 4
- YRMUGERSMQJNSC-UHFFFAOYSA-N 2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)acetonitrile Chemical compound ClC=1C(=C2C(=NC=1)NC=C2)CC#N YRMUGERSMQJNSC-UHFFFAOYSA-N 0.000 description 4
- TWWISNNONCPWPM-ZDUSSCGKSA-N 2-[(1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]acetonitrile Chemical compound C[C@@H]1N(CCC2=C1C=CC=C2CC#N)C(=O)CC1=C(Cl)C=CC=C1Cl TWWISNNONCPWPM-ZDUSSCGKSA-N 0.000 description 4
- IFONQEGIKZHAEC-UHFFFAOYSA-N 2-[(2,4-dimethoxyphenyl)methyl]-4,4-difluoro-1-methyl-1,3-dihydroisoquinoline Chemical compound COC1=C(CN2C(C3=CC=CC=C3C(C2)(F)F)C)C=CC(=C1)OC IFONQEGIKZHAEC-UHFFFAOYSA-N 0.000 description 4
- UKIYLORHZIGTSN-AWEZNQCLSA-N 2-[(4-methylphenyl)sulfonyl-[(1S)-1-phenylethyl]amino]acetic acid Chemical compound CC1=CC=C(C=C1)S(=O)(=O)N([C@@H](C)C1=CC=CC=C1)CC(=O)O UKIYLORHZIGTSN-AWEZNQCLSA-N 0.000 description 4
- QGYITPQJFPCDLU-UHFFFAOYSA-N 2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinoline-5-carbonitrile Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1C(C=2C=CC=C(C=2CC1)C#N)C QGYITPQJFPCDLU-UHFFFAOYSA-N 0.000 description 4
- DZWQOBDLOFXIKA-UHFFFAOYSA-N 3,5-dichloro-2-methoxypyridin-4-amine Chemical compound ClC=1C(=NC=C(C=1N)Cl)OC DZWQOBDLOFXIKA-UHFFFAOYSA-N 0.000 description 4
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 4
- XYPKOVNHRMXWKO-UHFFFAOYSA-N 5-chloro-4-iodo-1H-indazole Chemical compound ClC=1C(=C2C=NNC2=CC=1)I XYPKOVNHRMXWKO-UHFFFAOYSA-N 0.000 description 4
- IUCHSFLGJZJMLN-LLTODGECSA-N 6-[(1S)-1-methyl-1,2,3,4-tetrahydroisoquinolin-5-yl]morpholin-3-one Chemical class C[C@@H]1NCCC2=C1C=CC=C2C1CNC(=O)CO1 IUCHSFLGJZJMLN-LLTODGECSA-N 0.000 description 4
- PPAKSFPSRMJQQH-GUYCJALGSA-N C[C@@H]1N(C[C@@H](C2=CC=CC=C12)O)S(=O)(=O)C1=CC=C(C=C1)C Chemical compound C[C@@H]1N(C[C@@H](C2=CC=CC=C12)O)S(=O)(=O)C1=CC=C(C=C1)C PPAKSFPSRMJQQH-GUYCJALGSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- OFKDYCMYTGQBIX-UHFFFAOYSA-N N-(2,3-dichlorophenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)NC(=O)N1C(C2=CC=CC=C2CC1)C OFKDYCMYTGQBIX-UHFFFAOYSA-N 0.000 description 4
- MQGBDRZWPMGKLY-UHFFFAOYSA-N N-(2,4-dichlorophenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound ClC1=C(C=CC(=C1)Cl)NC(=O)N1C(C2=CC=CC=C2CC1)C MQGBDRZWPMGKLY-UHFFFAOYSA-N 0.000 description 4
- NNAGIUAAGNEDIR-UHFFFAOYSA-N N-(2,6-dimethylphenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound CC1=C(C(=CC=C1)C)NC(=O)N1C(C2=CC=CC=C2CC1)C NNAGIUAAGNEDIR-UHFFFAOYSA-N 0.000 description 4
- NNCYHQAVFRGUBF-UHFFFAOYSA-N N-(2-bromophenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound BrC1=C(C=CC=C1)NC(=O)N1C(C2=CC=CC=C2CC1)C NNCYHQAVFRGUBF-UHFFFAOYSA-N 0.000 description 4
- BERXXVMLFCHFAQ-UHFFFAOYSA-N N-(2-fluorophenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound FC1=C(C=CC=C1)NC(=O)N1C(C2=CC=CC=C2CC1)C BERXXVMLFCHFAQ-UHFFFAOYSA-N 0.000 description 4
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 125000002252 acyl group Chemical group 0.000 description 4
- 125000004103 aminoalkyl group Chemical group 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 230000009286 beneficial effect Effects 0.000 description 4
- MUALRAIOVNYAIW-UHFFFAOYSA-N binap Chemical compound C1=CC=CC=C1P(C=1C(=C2C=CC=CC2=CC=1)C=1C2=CC=CC=C2C=CC=1P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 MUALRAIOVNYAIW-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N chloroform Substances ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- GKIRPKYJQBWNGO-OCEACIFDSA-N clomifene Chemical compound C1=CC(OCCN(CC)CC)=CC=C1C(\C=1C=CC=CC=1)=C(\Cl)C1=CC=CC=C1 GKIRPKYJQBWNGO-OCEACIFDSA-N 0.000 description 4
- 239000012230 colorless oil Substances 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- WQOXQRCZOLPYPM-UHFFFAOYSA-N dimethyl disulfide Chemical group CSSC WQOXQRCZOLPYPM-UHFFFAOYSA-N 0.000 description 4
- 201000010099 disease Diseases 0.000 description 4
- 208000035475 disorder Diseases 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 235000019253 formic acid Nutrition 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 239000005457 ice water Substances 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 239000003446 ligand Substances 0.000 description 4
- LDDHMLJTFXJGPI-UHFFFAOYSA-N memantine hydrochloride Chemical compound Cl.C1C(C2)CC3(C)CC1(C)CC2(N)C3 LDDHMLJTFXJGPI-UHFFFAOYSA-N 0.000 description 4
- JEOVCKQSVVSXMU-QMMMGPOBSA-N methyl (1S)-1-methyl-1,2,3,4-tetrahydroisoquinoline-5-carboxylate Chemical compound C[C@@H]1NCCC=2C(=CC=CC1=2)C(=O)OC JEOVCKQSVVSXMU-QMMMGPOBSA-N 0.000 description 4
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 4
- PQIOSYKVBBWRRI-UHFFFAOYSA-N methylphosphonyl difluoride Chemical group CP(F)(F)=O PQIOSYKVBBWRRI-UHFFFAOYSA-N 0.000 description 4
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 description 4
- 238000002414 normal-phase solid-phase extraction Methods 0.000 description 4
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 4
- 150000002940 palladium Chemical class 0.000 description 4
- 229910052763 palladium Inorganic materials 0.000 description 4
- 125000003386 piperidinyl group Chemical group 0.000 description 4
- 229940126027 positive allosteric modulator Drugs 0.000 description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 description 4
- FASDKYOPVNHBLU-ZETCQYMHSA-N pramipexole Chemical compound C1[C@@H](NCCC)CCC2=C1SC(N)=N2 FASDKYOPVNHBLU-ZETCQYMHSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 4
- YHJIGQIWLFZKQN-JTQLQIEISA-N tert-butyl (1S)-5-bromo-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound BrC1=C2CCN([C@H](C2=CC=C1)C)C(=O)OC(C)(C)C YHJIGQIWLFZKQN-JTQLQIEISA-N 0.000 description 4
- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 4
- 238000004809 thin layer chromatography Methods 0.000 description 4
- 125000003396 thiol group Chemical group [H]S* 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- 238000004704 ultra performance liquid chromatography Methods 0.000 description 4
- CXNIUSPIQKWYAI-UHFFFAOYSA-N xantphos Chemical compound C=12OC3=C(P(C=4C=CC=CC=4)C=4C=CC=CC=4)C=CC=C3C(C)(C)C2=CC=CC=1P(C=1C=CC=CC=1)C1=CC=CC=C1 CXNIUSPIQKWYAI-UHFFFAOYSA-N 0.000 description 4
- IKFRHDBFUZKIBM-QRPNPIFTSA-N (1S)-1-methyl-5-methylsulfonyl-1,2,3,4-tetrahydroisoquinoline hydrochloride Chemical compound Cl.C[C@@H]1NCCc2c1cccc2S(C)(=O)=O IKFRHDBFUZKIBM-QRPNPIFTSA-N 0.000 description 3
- ALWVFJCCPZFJJH-KRWDZBQOSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-N,N-di(propan-2-yl)-3,4-dihydro-1H-isoquinoline-5-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C(=O)N(C(C)C)C(C)C)C ALWVFJCCPZFJJH-KRWDZBQOSA-N 0.000 description 3
- REIKCVUSKMBFKX-HNNXBMFYSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-N-pyridin-2-yl-3,4-dihydro-1H-isoquinoline-5-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C(=O)NC1=NC=CC=C1)C REIKCVUSKMBFKX-HNNXBMFYSA-N 0.000 description 3
- HMWWXWYWVDLTSE-LBPRGKRZSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-N,1-dimethyl-3,4-dihydro-1H-isoquinoline-5-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C(=O)NC)C HMWWXWYWVDLTSE-LBPRGKRZSA-N 0.000 description 3
- SRLTXOBTZZNBCQ-ZDUSSCGKSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-N,N,1-trimethyl-3,4-dihydro-1H-isoquinoline-5-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C(=O)N(C)C)C SRLTXOBTZZNBCQ-ZDUSSCGKSA-N 0.000 description 3
- GQLDKRHWSODCHU-OIBJUYFYSA-N (1S,4S)-1-methyl-1,2,3,4-tetrahydroisoquinolin-4-ol Chemical compound C[C@@H]1NC[C@H](C2=CC=CC=C12)O GQLDKRHWSODCHU-OIBJUYFYSA-N 0.000 description 3
- PPAKSFPSRMJQQH-SUMWQHHRSA-N (1S,4S)-1-methyl-2-(4-methylphenyl)sulfonyl-3,4-dihydro-1H-isoquinolin-4-ol Chemical compound C[C@@H]1N(C[C@@H](O)C2=C1C=CC=C2)S(=O)(=O)C1=CC=C(C)C=C1 PPAKSFPSRMJQQH-SUMWQHHRSA-N 0.000 description 3
- RBZWBNPBOMHNHO-UHFFFAOYSA-N (5-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)methyl methanesulfonate Chemical compound CS(=O)(=O)OCC1=C2C(=NC=C1Cl)NC=C2 RBZWBNPBOMHNHO-UHFFFAOYSA-N 0.000 description 3
- UOBLQIKFQVPGRA-UHFFFAOYSA-N 1-(5-bromo-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl)-2-(2,6-dichlorophenyl)ethanone Chemical compound BrC1=C2CCN(C(C2=CC=C1)C)C(CC1=C(C=CC=C1Cl)Cl)=O UOBLQIKFQVPGRA-UHFFFAOYSA-N 0.000 description 3
- JRSXZJXUCSYNGP-UHFFFAOYSA-N 1-methyl-n-(2-methylphenyl)-3,4-dihydro-1h-isoquinoline-2-carboxamide Chemical compound C1CC2=CC=CC=C2C(C)N1C(=O)NC1=CC=CC=C1C JRSXZJXUCSYNGP-UHFFFAOYSA-N 0.000 description 3
- KYSSMAJDZWFOSM-SRDKQIOZSA-N 2,2,2-trifluoro-1-[(1S)-1-methyl-1,2,3,4-tetrahydroisoquinolin-5-yl]ethanol hydrochloride Chemical compound Cl.C[C@@H]1NCCc2c(cccc12)C(O)C(F)(F)F KYSSMAJDZWFOSM-SRDKQIOZSA-N 0.000 description 3
- FJJMYFGRRPXIQI-UHFFFAOYSA-N 2-(2,6-dichloro-4-methoxycarbonylphenyl)acetic acid Chemical compound ClC1=C(C(=CC(=C1)C(=O)OC)Cl)CC(=O)O FJJMYFGRRPXIQI-UHFFFAOYSA-N 0.000 description 3
- NFABMQBFRVQFIC-ZDUSSCGKSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-5-(4,5-dihydro-1H-imidazol-2-yl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C=1NCCN=1)C NFABMQBFRVQFIC-ZDUSSCGKSA-N 0.000 description 3
- INRYRGOCXKASRB-ZDUSSCGKSA-N 2-(2-bromo-6-methoxyphenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound BrC1=C(C(=CC=C1)OC)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C INRYRGOCXKASRB-ZDUSSCGKSA-N 0.000 description 3
- DYUHSHZRQWHRRN-UHFFFAOYSA-N 2-[(2,4-dimethoxyphenyl)methyl]-4,4-difluoro-1-methyl-1H-isoquinolin-3-one Chemical compound COC1=C(CN2C(C3=CC=CC=C3C(C2=O)(F)F)C)C=CC(=C1)OC DYUHSHZRQWHRRN-UHFFFAOYSA-N 0.000 description 3
- PCCKECKDOJJGBE-LBPRGKRZSA-N 3-chloro-2-[2-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]benzoic acid Chemical compound ClC=1C(=C(C(=O)O)C=CC=1)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C PCCKECKDOJJGBE-LBPRGKRZSA-N 0.000 description 3
- MKPIKRDCFGEBEK-UHFFFAOYSA-N 7-bromo-1-methyl-1,2,3,4-tetrahydroisoquinoline hydrochloride Chemical compound Cl.CC1NCCc2ccc(Br)cc12 MKPIKRDCFGEBEK-UHFFFAOYSA-N 0.000 description 3
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 239000012448 Lithium borohydride Substances 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- DGGPQRATAOCBML-UHFFFAOYSA-N N-(8-methyl-1,2,3,4-tetrahydroisoquinolin-5-yl)methanesulfonamide hydrochloride Chemical compound Cl.Cc1ccc(NS(C)(=O)=O)c2CCNCc12 DGGPQRATAOCBML-UHFFFAOYSA-N 0.000 description 3
- NVTVJHYKELSKIC-QRPNPIFTSA-N N-[(1S)-1-methyl-1,2,3,4-tetrahydroisoquinolin-5-yl]methanesulfonamide hydrochloride Chemical compound Cl.C[C@@H]1NCCc2c(NS(C)(=O)=O)cccc12 NVTVJHYKELSKIC-QRPNPIFTSA-N 0.000 description 3
- JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- XSVMFMHYUFZWBK-NSHDSACASA-N Rivastigmine Chemical compound CCN(C)C(=O)OC1=CC=CC([C@H](C)N(C)C)=C1 XSVMFMHYUFZWBK-NSHDSACASA-N 0.000 description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 3
- 239000012346 acetyl chloride Substances 0.000 description 3
- 125000004442 acylamino group Chemical group 0.000 description 3
- 125000003282 alkyl amino group Chemical group 0.000 description 3
- 125000005907 alkyl ester group Chemical group 0.000 description 3
- 239000000164 antipsychotic agent Substances 0.000 description 3
- 229940005529 antipsychotics Drugs 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 125000001246 bromo group Chemical group Br* 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 3
- 229910000024 caesium carbonate Inorganic materials 0.000 description 3
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 150000001879 copper Chemical class 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 230000006806 disease prevention Effects 0.000 description 3
- XWAIAVWHZJNZQQ-UHFFFAOYSA-N donepezil hydrochloride Chemical compound [H+].[Cl-].O=C1C=2C=C(OC)C(OC)=CC=2CC1CC(CC1)CCN1CC1=CC=CC=C1 XWAIAVWHZJNZQQ-UHFFFAOYSA-N 0.000 description 3
- 239000002552 dosage form Substances 0.000 description 3
- 150000003840 hydrochlorides Chemical class 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- DSDSZSSATAFGOF-LBPRGKRZSA-N methyl (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinoline-5-carboxylate Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C(=O)OC)C DSDSZSSATAFGOF-LBPRGKRZSA-N 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 230000035790 physiological processes and functions Effects 0.000 description 3
- 229960003089 pramipexole Drugs 0.000 description 3
- UHSKFQJFRQCDBE-UHFFFAOYSA-N ropinirole Chemical compound CCCN(CCC)CCC1=CC=CC2=C1CC(=O)N2 UHSKFQJFRQCDBE-UHFFFAOYSA-N 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- MEZLKOACVSPNER-GFCCVEGCSA-N selegiline Chemical compound C#CCN(C)[C@H](C)CC1=CC=CC=C1 MEZLKOACVSPNER-GFCCVEGCSA-N 0.000 description 3
- 150000003384 small molecules Chemical class 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- 239000012453 solvate Substances 0.000 description 3
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 description 3
- QWHFXPBBVCAWJQ-NSHDSACASA-N tert-butyl (1S)-1-methyl-5-methylsulfonyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound C[C@@H]1N(CCC2=C(C=CC=C12)S(=O)(=O)C)C(=O)OC(C)(C)C QWHFXPBBVCAWJQ-NSHDSACASA-N 0.000 description 3
- MBEGRCQVNUSEEZ-VPHXOMNUSA-N tert-butyl (1S)-5-(1-hydroxy-2-nitroethyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound OC(C[N+](=O)[O-])C1=C2CCN([C@H](C2=CC=C1)C)C(=O)OC(C)(C)C MBEGRCQVNUSEEZ-VPHXOMNUSA-N 0.000 description 3
- OTVHPFUQANAEGW-NSHDSACASA-N tert-butyl (1S)-5-formyl-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound C(=O)C1=C2CCN([C@H](C2=CC=C1)C)C(=O)OC(C)(C)C OTVHPFUQANAEGW-NSHDSACASA-N 0.000 description 3
- LEIMLDGFXIOXMT-UHFFFAOYSA-N trimethylsilyl cyanide Chemical compound C[Si](C)(C)C#N LEIMLDGFXIOXMT-UHFFFAOYSA-N 0.000 description 3
- PMXIQDLWZGKMRF-LBPRGKRZSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-N-(1H-1,2,4-triazol-5-yl)-3,4-dihydro-1H-isoquinoline-5-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C(=O)NC1=NN=CN1)C PMXIQDLWZGKMRF-LBPRGKRZSA-N 0.000 description 2
- XJXXMWCYUJMTOU-LBPRGKRZSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-N-(2,2,2-trifluoroethyl)-3,4-dihydro-1H-isoquinoline-5-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C(=O)NCC(F)(F)F)C XJXXMWCYUJMTOU-LBPRGKRZSA-N 0.000 description 2
- GNEBWGGAWPGZMM-AWEZNQCLSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-N-propan-2-yl-3,4-dihydro-1H-isoquinoline-5-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C(=O)NC(C)C)C GNEBWGGAWPGZMM-AWEZNQCLSA-N 0.000 description 2
- LECWWZVJSFYUAL-ZETCQYMHSA-N (1S)-5-bromo-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid Chemical compound C[C@H]1C2=C(CCN1C(=O)O)C(=CC=C2)Br LECWWZVJSFYUAL-ZETCQYMHSA-N 0.000 description 2
- GQLDKRHWSODCHU-XVKPBYJWSA-N (1S,4R)-1-methyl-1,2,3,4-tetrahydroisoquinolin-4-ol Chemical compound C[C@@H]1NC[C@@H](C2=CC=CC=C12)O GQLDKRHWSODCHU-XVKPBYJWSA-N 0.000 description 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 description 2
- KWTSXDURSIMDCE-QMMMGPOBSA-N (S)-amphetamine Chemical compound C[C@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-QMMMGPOBSA-N 0.000 description 2
- VMKAFJQFKBASMU-QGZVFWFLSA-N (r)-2-methyl-cbs-oxazaborolidine Chemical compound C([C@@H]12)CCN1B(C)OC2(C=1C=CC=CC=1)C1=CC=CC=C1 VMKAFJQFKBASMU-QGZVFWFLSA-N 0.000 description 2
- SCXREHYVJCTSER-UHFFFAOYSA-N 1-[5-(aminomethyl)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-(2,6-dichlorophenyl)ethanone 2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.CC1N(CCc2c(CN)cccc12)C(=O)Cc1c(Cl)cccc1Cl SCXREHYVJCTSER-UHFFFAOYSA-N 0.000 description 2
- QPILYVQSKNWRDD-UHFFFAOYSA-N 1-methyl-1,2,3,4-tetrahydroisoquinoline Chemical compound C1=CC=C2C(C)NCCC2=C1 QPILYVQSKNWRDD-UHFFFAOYSA-N 0.000 description 2
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
- AXVMMTQNEXNSDI-RGENBBCFSA-N 2,2,2-trifluoro-1-[(1S)-1-methyl-1,2,3,4-tetrahydroisoquinolin-5-yl]ethanol Chemical compound FC(C(O)C1=C2CCN[C@H](C2=CC=C1)C)(F)F AXVMMTQNEXNSDI-RGENBBCFSA-N 0.000 description 2
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 2
- RDKYJKZEYXPWSS-BTDLBPIBSA-N 2-(2,6-dichloro-4-fluorophenyl)-1-[(1S,4R)-4-hydroxy-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC(=C1)F)Cl)CC(=O)N1[C@H](C2=CC=CC=C2[C@H](C1)O)C RDKYJKZEYXPWSS-BTDLBPIBSA-N 0.000 description 2
- QSPAZLKGXQHBEQ-PIJUOJQZSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-4-hydroxy-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC=C2C(C1)O)C QSPAZLKGXQHBEQ-PIJUOJQZSA-N 0.000 description 2
- UNVMEDILGAIEPM-IFGYVTRGSA-N 2-(2-chloro-6-fluorophenyl)-1-[(1S)-1-methyl-5-(2,2,2-trifluoro-1-hydroxyethyl)-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)F)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(C(F)(F)F)O)C UNVMEDILGAIEPM-IFGYVTRGSA-N 0.000 description 2
- BVKHCBMSGJTJAJ-LBPRGKRZSA-N 2-(2-chloro-6-nitrophenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)[N+](=O)[O-])CC(=O)N1[C@H](C2=CC=CC=C2CC1)C BVKHCBMSGJTJAJ-LBPRGKRZSA-N 0.000 description 2
- SPDSOXQKGPJGBE-NSHDSACASA-N 2-O-tert-butyl 5-O-methyl (1S)-1-methyl-3,4-dihydro-1H-isoquinoline-2,5-dicarboxylate Chemical compound C[C@@H]1N(CCC=2C(=CC=CC1=2)C(=O)OC)C(=O)OC(C)(C)C SPDSOXQKGPJGBE-NSHDSACASA-N 0.000 description 2
- ZBCODQPFVNDLTD-LBPRGKRZSA-N 2-[2-[(1S)-5-bromo-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxoethyl]-3-chlorobenzonitrile Chemical compound BrC1=C2CCN([C@H](C2=CC=C1)C)C(CC1=C(C#N)C=CC=C1Cl)=O ZBCODQPFVNDLTD-LBPRGKRZSA-N 0.000 description 2
- OQDPVLVUJFGPGQ-UHFFFAOYSA-N 2-[4-(1,3-benzodioxol-5-ylmethyl)-1-piperazinyl]pyrimidine Chemical compound C=1C=C2OCOC2=CC=1CN(CC1)CCN1C1=NC=CC=N1 OQDPVLVUJFGPGQ-UHFFFAOYSA-N 0.000 description 2
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 2
- 229960000549 4-dimethylaminophenol Drugs 0.000 description 2
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
- IIEQAICPNKOLQI-LEMICQRHSA-N 6-[(1S)-1-methyl-1,2,3,4-tetrahydroisoquinolin-5-yl]morpholin-3-one hydrochloride Chemical compound Cl.C[C@@H]1NCCc2c1cccc2C1CNC(=O)CO1 IIEQAICPNKOLQI-LEMICQRHSA-N 0.000 description 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- LPJKCPQBAVUOIP-FJXQXJEOSA-N Cl.BrC1=C2CCN[C@H](C2=CC=C1)C Chemical compound Cl.BrC1=C2CCN[C@H](C2=CC=C1)C LPJKCPQBAVUOIP-FJXQXJEOSA-N 0.000 description 2
- GJSURZIOUXUGAL-UHFFFAOYSA-N Clonidine Chemical compound ClC1=CC=CC(Cl)=C1NC1=NCCN1 GJSURZIOUXUGAL-UHFFFAOYSA-N 0.000 description 2
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 2
- HCYAFALTSJYZDH-UHFFFAOYSA-N Desimpramine Chemical compound C1CC2=CC=CC=C2N(CCCNC)C2=CC=CC=C21 HCYAFALTSJYZDH-UHFFFAOYSA-N 0.000 description 2
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 2
- 235000004694 Eucalyptus leucoxylon Nutrition 0.000 description 2
- 244000166102 Eucalyptus leucoxylon Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 2
- 102000010909 Monoamine Oxidase Human genes 0.000 description 2
- 108010062431 Monoamine oxidase Proteins 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- HOKKHZGPKSLGJE-GSVOUGTGSA-N N-Methyl-D-aspartic acid Chemical compound CN[C@@H](C(O)=O)CC(O)=O HOKKHZGPKSLGJE-GSVOUGTGSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 235000019502 Orange oil Nutrition 0.000 description 2
- 101150003085 Pdcl gene Proteins 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- 229940121991 Serotonin and norepinephrine reuptake inhibitor Drugs 0.000 description 2
- 238000006069 Suzuki reaction reaction Methods 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 description 2
- 150000001299 aldehydes Chemical group 0.000 description 2
- 150000001345 alkine derivatives Chemical group 0.000 description 2
- 239000002168 alkylating agent Substances 0.000 description 2
- 229940100198 alkylating agent Drugs 0.000 description 2
- DKNWSYNQZKUICI-UHFFFAOYSA-N amantadine Chemical compound C1C(C2)CC3CC2CC1(N)C3 DKNWSYNQZKUICI-UHFFFAOYSA-N 0.000 description 2
- 229960003805 amantadine Drugs 0.000 description 2
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 2
- 239000005557 antagonist Substances 0.000 description 2
- 239000000935 antidepressant agent Substances 0.000 description 2
- 229940005513 antidepressants Drugs 0.000 description 2
- VMWNQDUVQKEIOC-CYBMUJFWSA-N apomorphine Chemical compound C([C@H]1N(C)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 VMWNQDUVQKEIOC-CYBMUJFWSA-N 0.000 description 2
- 229940049706 benzodiazepine Drugs 0.000 description 2
- 150000001557 benzodiazepines Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 2
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 2
- YKPUWZUDDOIDPM-SOFGYWHQSA-N capsaicin Chemical compound COC1=CC(CNC(=O)CCCC\C=C\C(C)C)=CC=C1O YKPUWZUDDOIDPM-SOFGYWHQSA-N 0.000 description 2
- 125000002837 carbocyclic group Chemical group 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical group 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical group OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 2
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 2
- DGBIGWXXNGSACT-UHFFFAOYSA-N clonazepam Chemical compound C12=CC([N+](=O)[O-])=CC=C2NC(=O)CN=C1C1=CC=CC=C1Cl DGBIGWXXNGSACT-UHFFFAOYSA-N 0.000 description 2
- 229960003120 clonazepam Drugs 0.000 description 2
- 229960002896 clonidine Drugs 0.000 description 2
- 238000002648 combination therapy Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 229960003914 desipramine Drugs 0.000 description 2
- NKLCNNUWBJBICK-UHFFFAOYSA-N dess–martin periodinane Chemical compound C1=CC=C2I(OC(=O)C)(OC(C)=O)(OC(C)=O)OC(=O)C2=C1 NKLCNNUWBJBICK-UHFFFAOYSA-N 0.000 description 2
- 229910052805 deuterium Inorganic materials 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 229960003529 diazepam Drugs 0.000 description 2
- AAOVKJBEBIDNHE-UHFFFAOYSA-N diazepam Chemical compound N=1CC(=O)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 AAOVKJBEBIDNHE-UHFFFAOYSA-N 0.000 description 2
- 125000000950 dibromo group Chemical group Br* 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000006274 endogenous ligand Substances 0.000 description 2
- JRURYQJSLYLRLN-BJMVGYQFSA-N entacapone Chemical compound CCN(CC)C(=O)C(\C#N)=C\C1=CC(O)=C(O)C([N+]([O-])=O)=C1 JRURYQJSLYLRLN-BJMVGYQFSA-N 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 238000002868 homogeneous time resolved fluorescence Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- BCGWQEUPMDMJNV-UHFFFAOYSA-N imipramine Chemical compound C1CC2=CC=CC=C2N(CCCN(C)C)C2=CC=CC=C21 BCGWQEUPMDMJNV-UHFFFAOYSA-N 0.000 description 2
- 229960004801 imipramine Drugs 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
- 125000000468 ketone group Chemical group 0.000 description 2
- 239000012280 lithium aluminium hydride Substances 0.000 description 2
- 239000007937 lozenge Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- 238000004949 mass spectrometry Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229960004640 memantine Drugs 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 2
- KZVQLTXPBQRFGI-PPHPATTJSA-N methyl 3-[(1S)-1-methyl-1,2,3,4-tetrahydroisoquinolin-5-yl]propanoate hydrochloride Chemical compound Cl.COC(=O)CCc1cccc2[C@H](C)NCCc12 KZVQLTXPBQRFGI-PPHPATTJSA-N 0.000 description 2
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 2
- VSEAAEQOQBMPQF-UHFFFAOYSA-N morpholin-3-one Chemical compound O=C1COCCN1 VSEAAEQOQBMPQF-UHFFFAOYSA-N 0.000 description 2
- 229940126662 negative allosteric modulator Drugs 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- 239000010502 orange oil Substances 0.000 description 2
- 125000006299 oxetan-3-yl group Chemical group [H]C1([H])OC([H])([H])C1([H])* 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- MUJIDPITZJWBSW-UHFFFAOYSA-N palladium(2+) Chemical compound [Pd+2] MUJIDPITZJWBSW-UHFFFAOYSA-N 0.000 description 2
- LXNAVEXFUKBNMK-UHFFFAOYSA-N palladium(II) acetate Substances [Pd].CC(O)=O.CC(O)=O LXNAVEXFUKBNMK-UHFFFAOYSA-N 0.000 description 2
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 2
- 238000007911 parenteral administration Methods 0.000 description 2
- 229960004310 piribedil Drugs 0.000 description 2
- 229910000160 potassium phosphate Inorganic materials 0.000 description 2
- 235000011009 potassium phosphates Nutrition 0.000 description 2
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229960001534 risperidone Drugs 0.000 description 2
- RAPZEAPATHNIPO-UHFFFAOYSA-N risperidone Chemical compound FC1=CC=C2C(C3CCN(CC3)CCC=3C(=O)N4CCCCC4=NC=3C)=NOC2=C1 RAPZEAPATHNIPO-UHFFFAOYSA-N 0.000 description 2
- KFQYTPMOWPVWEJ-INIZCTEOSA-N rotigotine Chemical compound CCCN([C@@H]1CC2=CC=CC(O)=C2CC1)CCC1=CC=CS1 KFQYTPMOWPVWEJ-INIZCTEOSA-N 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 229940124834 selective serotonin reuptake inhibitor Drugs 0.000 description 2
- 239000012896 selective serotonin reuptake inhibitor Substances 0.000 description 2
- 239000003775 serotonin noradrenalin reuptake inhibitor Substances 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 238000010898 silica gel chromatography Methods 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000012312 sodium hydride Substances 0.000 description 2
- 229910000104 sodium hydride Inorganic materials 0.000 description 2
- RMBAVIFYHOYIFM-UHFFFAOYSA-M sodium methanethiolate Chemical compound [Na+].[S-]C RMBAVIFYHOYIFM-UHFFFAOYSA-M 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 2
- ZQKRSQBXSICCKW-NSHDSACASA-N tert-butyl (1S)-5-(hydroxymethyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound OCC1=C2CCN([C@H](C2=CC=C1)C)C(=O)OC(C)(C)C ZQKRSQBXSICCKW-NSHDSACASA-N 0.000 description 2
- OGZYPZCIGVWZLD-NSHDSACASA-N tert-butyl (1S)-5-(methanesulfonamido)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound C[C@@H]1N(CCC2=C(C=CC=C12)NS(=O)(=O)C)C(=O)OC(C)(C)C OGZYPZCIGVWZLD-NSHDSACASA-N 0.000 description 2
- FRHFXCLSLTUMOM-LXKVQUBZSA-N tert-butyl (1S)-5-[(E)-3-methoxy-3-oxoprop-1-enyl]-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound COC(/C=C/C1=C2CCN([C@H](C2=CC=C1)C)C(=O)OC(C)(C)C)=O FRHFXCLSLTUMOM-LXKVQUBZSA-N 0.000 description 2
- KWVOPIOERWGBHA-HKALDPMFSA-N tert-butyl (1S)-5-[2-[(2-chloroacetyl)amino]-1-hydroxyethyl]-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound ClCC(=O)NCC(O)C1=C2CCN([C@H](C2=CC=C1)C)C(=O)OC(C)(C)C KWVOPIOERWGBHA-HKALDPMFSA-N 0.000 description 2
- ZYKGQBWJSBEIAF-UHFFFAOYSA-N tert-butyl 1-methyl-3,4-dihydro-1h-isoquinoline-2-carboxylate Chemical compound C1=CC=C2C(C)N(C(=O)OC(C)(C)C)CCC2=C1 ZYKGQBWJSBEIAF-UHFFFAOYSA-N 0.000 description 2
- BFNYNEMRWHFIMR-UHFFFAOYSA-N tert-butyl 2-cyanoacetate Chemical compound CC(C)(C)OC(=O)CC#N BFNYNEMRWHFIMR-UHFFFAOYSA-N 0.000 description 2
- OGZYPZCIGVWZLD-UHFFFAOYSA-N tert-butyl 5-(methanesulfonamido)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound CC1N(CCC2=C1C=CC=C2NS(C)(=O)=O)C(=O)OC(C)(C)C OGZYPZCIGVWZLD-UHFFFAOYSA-N 0.000 description 2
- IOGXOCVLYRDXLW-UHFFFAOYSA-N tert-butyl nitrite Chemical compound CC(C)(C)ON=O IOGXOCVLYRDXLW-UHFFFAOYSA-N 0.000 description 2
- 239000012414 tert-butyl nitrite Substances 0.000 description 2
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 2
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 238000000844 transformation Methods 0.000 description 2
- QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 description 2
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 2
- BRVQQHPKPWSRQU-ZDUSSCGKSA-N (1S)-2-[2-(2,6-dichlorophenyl)acetyl]-N-ethyl-1-methyl-3,4-dihydro-1H-isoquinoline-5-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C=2C=CC=C(C=2CC1)C(=O)NCC)C BRVQQHPKPWSRQU-ZDUSSCGKSA-N 0.000 description 1
- VJGXOACAPIGNKO-NSHDSACASA-N (1S)-N-(2,6-dichlorophenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)NC(=O)N1[C@H](C2=CC=CC=C2CC1)C VJGXOACAPIGNKO-NSHDSACASA-N 0.000 description 1
- CMWLWNUPWSLAMB-NSHDSACASA-N (1S)-N-(2,6-dichlorophenyl)-1-methyl-5-methylsulfonyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)NC(=O)N1[C@H](C2=CC=CC(=C2CC1)S(=O)(=O)C)C CMWLWNUPWSLAMB-NSHDSACASA-N 0.000 description 1
- OTYALRNHSCZPDG-NSHDSACASA-N (1S)-N-(2,6-dichlorophenyl)-5-(hydroxymethyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)NC(=O)N1[C@H](C2=CC=CC(=C2CC1)CO)C OTYALRNHSCZPDG-NSHDSACASA-N 0.000 description 1
- JGSWXBCVCWXNII-NSHDSACASA-N (1S)-N-(2,6-dichlorophenyl)-5-(methanesulfonamido)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)NC(=O)N1[C@H](C2=CC=CC(=C2CC1)NS(=O)(=O)C)C JGSWXBCVCWXNII-NSHDSACASA-N 0.000 description 1
- NNAGIUAAGNEDIR-HNNXBMFYSA-N (1S)-N-(2,6-dimethylphenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound CC1=C(C(=CC=C1)C)NC(=O)N1[C@H](C2=CC=CC=C2CC1)C NNAGIUAAGNEDIR-HNNXBMFYSA-N 0.000 description 1
- ZSOPVUPULBKTCQ-NSHDSACASA-N (1S)-N-(2-bromo-6-fluorophenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound BrC1=C(C(=CC=C1)F)NC(=O)N1[C@H](C2=CC=CC=C2CC1)C ZSOPVUPULBKTCQ-NSHDSACASA-N 0.000 description 1
- QOAUXJGHYDWTRN-LBPRGKRZSA-N (1S)-N-(2-bromo-6-methoxyphenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound BrC1=C(C(=CC=C1)OC)NC(=O)N1[C@H](C2=CC=CC=C2CC1)C QOAUXJGHYDWTRN-LBPRGKRZSA-N 0.000 description 1
- NNCYHQAVFRGUBF-LBPRGKRZSA-N (1S)-N-(2-bromophenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound BrC1=C(C=CC=C1)NC(=O)N1[C@H](C2=CC=CC=C2CC1)C NNCYHQAVFRGUBF-LBPRGKRZSA-N 0.000 description 1
- YWSALMYNNFUEEZ-ZDUSSCGKSA-N (1S)-N-(2-chloro-6-methylphenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound ClC1=C(C(=CC=C1)C)NC(=O)N1[C@H](C2=CC=CC=C2CC1)C YWSALMYNNFUEEZ-ZDUSSCGKSA-N 0.000 description 1
- OXEUWLUBSNWQEA-NSHDSACASA-N (1S)-N-(5-bromo-2-chlorophenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound C[C@@H]1N(CCC2=C1C=CC=C2)C(=O)NC1=C(Cl)C=CC(Br)=C1 OXEUWLUBSNWQEA-NSHDSACASA-N 0.000 description 1
- WBUIHUIBJWJQBY-ZDUSSCGKSA-N (1S)-N-(cyanomethyl)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinoline-5-sulfonamide Chemical compound C(#N)CNS(=O)(=O)C=1C=2CCN([C@H](C=2C=CC=1)C)C(CC1=C(C=CC=C1Cl)Cl)=O WBUIHUIBJWJQBY-ZDUSSCGKSA-N 0.000 description 1
- XMZUHDZJOKXWTP-BONVTDFDSA-N (1S,4R)-N-(2,6-dichlorophenyl)-4-hydroxy-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound C[C@@H]1N(C[C@H](O)C2=C1C=CC=C2)C(=O)NC1=C(Cl)C=CC=C1Cl XMZUHDZJOKXWTP-BONVTDFDSA-N 0.000 description 1
- XMZUHDZJOKXWTP-ZUZCIYMTSA-N (1S,4S)-N-(2,6-dichlorophenyl)-4-hydroxy-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)NC(=O)N1[C@H](C2=CC=CC=C2[C@@H](C1)O)C XMZUHDZJOKXWTP-ZUZCIYMTSA-N 0.000 description 1
- FCYUPOCBNOAMHF-VGMFFHCQSA-N (1s)-1-phenylethanamine Chemical compound C[C@H](N)C1=CC=CC=C1.C[C@H](N)C1=CC=CC=C1 FCYUPOCBNOAMHF-VGMFFHCQSA-N 0.000 description 1
- VPKHWEFDYAMWOS-ZETCQYMHSA-N (1s)-5-bromo-1-methyl-1,2,3,4-tetrahydroisoquinoline Chemical compound C1=CC=C2[C@H](C)NCCC2=C1Br VPKHWEFDYAMWOS-ZETCQYMHSA-N 0.000 description 1
- SSJXIUAHEKJCMH-WDSKDSINSA-N (1s,2s)-cyclohexane-1,2-diamine Chemical compound N[C@H]1CCCC[C@@H]1N SSJXIUAHEKJCMH-WDSKDSINSA-N 0.000 description 1
- QOWBXWFYRXSBAS-UHFFFAOYSA-N (2,4-dimethoxyphenyl)methanamine Chemical compound COC1=CC=C(CN)C(OC)=C1 QOWBXWFYRXSBAS-UHFFFAOYSA-N 0.000 description 1
- VLPIATFUUWWMKC-SNVBAGLBSA-N (2r)-1-(2,6-dimethylphenoxy)propan-2-amine Chemical compound C[C@@H](N)COC1=C(C)C=CC=C1C VLPIATFUUWWMKC-SNVBAGLBSA-N 0.000 description 1
- DIIFZCPZIRQDIJ-UHFFFAOYSA-N (3,5-dimethyl-1,2-oxazol-4-yl)boronic acid Chemical compound CC1=NOC(C)=C1B(O)O DIIFZCPZIRQDIJ-UHFFFAOYSA-N 0.000 description 1
- PRRIGGBFRPGBRY-UHFFFAOYSA-N (3-diphenylphosphanyl-1-naphthalen-1-ylnaphthalen-2-yl)-diphenylphosphane Chemical group C1=CC=CC=C1P(C=1C(=C(C=2C3=CC=CC=C3C=CC=2)C2=CC=CC=C2C=1)P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 PRRIGGBFRPGBRY-UHFFFAOYSA-N 0.000 description 1
- VMKAFJQFKBASMU-KRWDZBQOSA-N (3as)-1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole Chemical compound C([C@H]12)CCN1B(C)OC2(C=1C=CC=CC=1)C1=CC=CC=C1 VMKAFJQFKBASMU-KRWDZBQOSA-N 0.000 description 1
- DIWRORZWFLOCLC-HNNXBMFYSA-N (3s)-7-chloro-5-(2-chlorophenyl)-3-hydroxy-1,3-dihydro-1,4-benzodiazepin-2-one Chemical compound N([C@H](C(NC1=CC=C(Cl)C=C11)=O)O)=C1C1=CC=CC=C1Cl DIWRORZWFLOCLC-HNNXBMFYSA-N 0.000 description 1
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 description 1
- RTHCYVBBDHJXIQ-MRXNPFEDSA-N (R)-fluoxetine Chemical compound O([C@H](CCNC)C=1C=CC=CC=1)C1=CC=C(C(F)(F)F)C=C1 RTHCYVBBDHJXIQ-MRXNPFEDSA-N 0.000 description 1
- 125000001359 1,2,3-triazol-4-yl group Chemical group [H]N1N=NC([*])=C1[H] 0.000 description 1
- 125000001305 1,2,4-triazol-3-yl group Chemical group [H]N1N=C([*])N=C1[H] 0.000 description 1
- PIMNFNXBTGPCIL-UHFFFAOYSA-N 1-(2-bromophenyl)ethanone Chemical compound CC(=O)C1=CC=CC=C1Br PIMNFNXBTGPCIL-UHFFFAOYSA-N 0.000 description 1
- MEJFSMMBMUHMAU-UHFFFAOYSA-N 1-bromo-2-(bromomethyl)-3-methoxybenzene Chemical compound COC1=CC=CC(Br)=C1CBr MEJFSMMBMUHMAU-UHFFFAOYSA-N 0.000 description 1
- JFTDNAXWZYOWHC-UHFFFAOYSA-N 1-bromo-3-(bromomethyl)-2,4-dichlorobenzene Chemical compound ClC1=CC=C(Br)C(Cl)=C1CBr JFTDNAXWZYOWHC-UHFFFAOYSA-N 0.000 description 1
- GQLDKRHWSODCHU-UHFFFAOYSA-N 1-methyl-1,2,3,4-tetrahydroisoquinolin-4-ol Chemical compound C1=CC=C2C(C)NCC(O)C2=C1 GQLDKRHWSODCHU-UHFFFAOYSA-N 0.000 description 1
- KEZNMOUMHOZFRA-UHFFFAOYSA-N 1h-pyrazol-4-ylboronic acid Chemical compound OB(O)C=1C=NNC=1 KEZNMOUMHOZFRA-UHFFFAOYSA-N 0.000 description 1
- 125000004778 2,2-difluoroethyl group Chemical group [H]C([H])(*)C([H])(F)F 0.000 description 1
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
- YAUYKCFMKMZTEX-UHFFFAOYSA-N 2,6-dichloro-4-fluoroaniline Chemical compound NC1=C(Cl)C=C(F)C=C1Cl YAUYKCFMKMZTEX-UHFFFAOYSA-N 0.000 description 1
- RDKYJKZEYXPWSS-DYZYQPBXSA-N 2-(2,6-dichloro-4-fluorophenyl)-1-[(1S,4S)-4-hydroxy-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC(=C1)F)Cl)CC(=O)N1[C@H](C2=CC=CC=C2[C@@H](C1)O)C RDKYJKZEYXPWSS-DYZYQPBXSA-N 0.000 description 1
- SUTPENAAFLOLOK-LBPRGKRZSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC=C2CC1)C SUTPENAAFLOLOK-LBPRGKRZSA-N 0.000 description 1
- SVWOSUUMPFKLAJ-HNNXBMFYSA-N 2-(2,6-dichlorophenyl)-1-[(1S)-1-methyl-5-[4-(trifluoromethyl)piperidine-1-carbonyl]-3,4-dihydro-1H-isoquinolin-2-yl]ethanone Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@H](C2=CC=CC(=C2CC1)C(=O)N1CCC(CC1)C(F)(F)F)C SVWOSUUMPFKLAJ-HNNXBMFYSA-N 0.000 description 1
- DVHQMZULSWDQIF-UHFFFAOYSA-N 2-(2-chloro-6-methoxyphenyl)acetic acid Chemical compound COC1=CC=CC(Cl)=C1CC(O)=O DVHQMZULSWDQIF-UHFFFAOYSA-N 0.000 description 1
- KTHGBTRAQOAOBS-UHFFFAOYSA-N 2-(2-chloro-6-nitrophenyl)acetic acid Chemical compound OC(=O)CC1=C(Cl)C=CC=C1[N+]([O-])=O KTHGBTRAQOAOBS-UHFFFAOYSA-N 0.000 description 1
- YFGHCGITMMYXAQ-UHFFFAOYSA-N 2-[(diphenylmethyl)sulfinyl]acetamide Chemical compound C=1C=CC=CC=1C(S(=O)CC(=O)N)C1=CC=CC=C1 YFGHCGITMMYXAQ-UHFFFAOYSA-N 0.000 description 1
- QVSWFQSUELDCNS-UHFFFAOYSA-N 2-[2-chloro-6-(trifluoromethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=C(Cl)C=CC=C1C(F)(F)F QVSWFQSUELDCNS-UHFFFAOYSA-N 0.000 description 1
- XWSGEVNYFYKXCP-UHFFFAOYSA-N 2-[carboxymethyl(methyl)amino]acetic acid Chemical compound OC(=O)CN(C)CC(O)=O XWSGEVNYFYKXCP-UHFFFAOYSA-N 0.000 description 1
- IMRWILPUOVGIMU-UHFFFAOYSA-N 2-bromopyridine Chemical compound BrC1=CC=CC=N1 IMRWILPUOVGIMU-UHFFFAOYSA-N 0.000 description 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 1
- SVEQHRSELNPKJJ-UHFFFAOYSA-N 2-methoxypyridin-4-amine Chemical compound COC1=CC(N)=CC=N1 SVEQHRSELNPKJJ-UHFFFAOYSA-N 0.000 description 1
- APIXJSLKIYYUKG-UHFFFAOYSA-N 3 Isobutyl 1 methylxanthine Chemical compound O=C1N(C)C(=O)N(CC(C)C)C2=C1N=CN2 APIXJSLKIYYUKG-UHFFFAOYSA-N 0.000 description 1
- LSVPLFVLCXIYHM-UHFFFAOYSA-N 3,4-dichloro-5-nitropyridine Chemical compound [O-][N+](=O)C1=CN=CC(Cl)=C1Cl LSVPLFVLCXIYHM-UHFFFAOYSA-N 0.000 description 1
- GLKVMXXYMNTCJX-UHFFFAOYSA-N 3-chloro-5-methylpyridin-4-amine Chemical compound CC1=CN=CC(Cl)=C1N GLKVMXXYMNTCJX-UHFFFAOYSA-N 0.000 description 1
- WBUOVKBZJOIOAE-UHFFFAOYSA-N 3-chlorobenzonitrile Chemical compound ClC1=CC=CC(C#N)=C1 WBUOVKBZJOIOAE-UHFFFAOYSA-N 0.000 description 1
- XPSYZCWYRWHVCC-UHFFFAOYSA-N 3-o-tert-butyl 1-o-methyl propanedioate Chemical compound COC(=O)CC(=O)OC(C)(C)C XPSYZCWYRWHVCC-UHFFFAOYSA-N 0.000 description 1
- PMXMIIMHBWHSKN-UHFFFAOYSA-N 3-{2-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]ethyl}-9-hydroxy-2-methyl-6,7,8,9-tetrahydropyrido[1,2-a]pyrimidin-4-one Chemical compound FC1=CC=C2C(C3CCN(CC3)CCC=3C(=O)N4CCCC(O)C4=NC=3C)=NOC2=C1 PMXMIIMHBWHSKN-UHFFFAOYSA-N 0.000 description 1
- YMHIEPNFCBNQQU-UHFFFAOYSA-N 4,4,5,5-tetramethyl-2-prop-2-enyl-1,3,2-dioxaborolane Chemical compound CC1(C)OB(CC=C)OC1(C)C YMHIEPNFCBNQQU-UHFFFAOYSA-N 0.000 description 1
- LAVZKLJDKGRZJG-UHFFFAOYSA-N 4-nitro-1h-indole Chemical compound [O-][N+](=O)C1=CC=CC2=C1C=CN2 LAVZKLJDKGRZJG-UHFFFAOYSA-N 0.000 description 1
- FDWFIQWULNKHOP-UHFFFAOYSA-N 5-bromo-2-(bromomethyl)-1,3-dichlorobenzene Chemical compound ClC1=CC(Br)=CC(Cl)=C1CBr FDWFIQWULNKHOP-UHFFFAOYSA-N 0.000 description 1
- BHOSWVZIGTVQNK-UHFFFAOYSA-N 5-chloro-1h-indazol-4-amine Chemical compound NC1=C(Cl)C=CC2=C1C=NN2 BHOSWVZIGTVQNK-UHFFFAOYSA-N 0.000 description 1
- PHZFFVFGFZWMFD-UHFFFAOYSA-N 5-chloro-1h-pyrrolo[2,3-b]pyridine-4-carbaldehyde Chemical compound ClC1=CN=C2NC=CC2=C1C=O PHZFFVFGFZWMFD-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- CEUORZQYGODEFX-UHFFFAOYSA-N Aripirazole Chemical compound ClC1=CC=CC(N2CCN(CCCCOC=3C=C4NC(=O)CCC4=CC=3)CC2)=C1Cl CEUORZQYGODEFX-UHFFFAOYSA-N 0.000 description 1
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- KPYSYYIEGFHWSV-UHFFFAOYSA-N Baclofen Chemical compound OC(=O)CC(CN)C1=CC=C(Cl)C=C1 KPYSYYIEGFHWSV-UHFFFAOYSA-N 0.000 description 1
- CYGODHVAJQTCBG-UHFFFAOYSA-N Bifeprunox Chemical compound C=12OC(=O)NC2=CC=CC=1N(CC1)CCN1CC(C=1)=CC=CC=1C1=CC=CC=C1 CYGODHVAJQTCBG-UHFFFAOYSA-N 0.000 description 1
- COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 description 1
- 239000002126 C01EB10 - Adenosine Substances 0.000 description 1
- LECWWZVJSFYUAL-UHFFFAOYSA-N CC(C1=CC=CC(Br)=C1CC1)N1C(O)=O Chemical compound CC(C1=CC=CC(Br)=C1CC1)N1C(O)=O LECWWZVJSFYUAL-UHFFFAOYSA-N 0.000 description 1
- 101100079984 Caenorhabditis elegans nhr-9 gene Proteins 0.000 description 1
- 229940127291 Calcium channel antagonist Drugs 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 102000000844 Cell Surface Receptors Human genes 0.000 description 1
- 108010001857 Cell Surface Receptors Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 1
- GDLIGKIOYRNHDA-UHFFFAOYSA-N Clomipramine Chemical compound C1CC2=CC=C(Cl)C=C2N(CCCN(C)C)C2=CC=CC=C21 GDLIGKIOYRNHDA-UHFFFAOYSA-N 0.000 description 1
- 229910021589 Copper(I) bromide Inorganic materials 0.000 description 1
- 241001480079 Corymbia calophylla Species 0.000 description 1
- IVOMOUWHDPKRLL-KQYNXXCUSA-N Cyclic adenosine monophosphate Chemical compound C([C@H]1O2)OP(O)(=O)O[C@H]1[C@@H](O)[C@@H]2N1C(N=CN=C2N)=C2N=C1 IVOMOUWHDPKRLL-KQYNXXCUSA-N 0.000 description 1
- 229940081615 DOPA decarboxylase inhibitor Drugs 0.000 description 1
- BUDQDWGNQVEFAC-UHFFFAOYSA-N Dihydropyran Chemical compound C1COC=CC1 BUDQDWGNQVEFAC-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- 102000015554 Dopamine receptor Human genes 0.000 description 1
- 108050004812 Dopamine receptor Proteins 0.000 description 1
- 208000012661 Dyskinesia Diseases 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 239000007995 HEPES buffer Substances 0.000 description 1
- 102000004384 Histamine H3 receptors Human genes 0.000 description 1
- 108090000981 Histamine H3 receptors Proteins 0.000 description 1
- 208000001953 Hypotension Diseases 0.000 description 1
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 description 1
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- WTDRDQBEARUVNC-LURJTMIESA-N L-DOPA Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-LURJTMIESA-N 0.000 description 1
- WTDRDQBEARUVNC-UHFFFAOYSA-N L-Dopa Natural products OC(=O)C(N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- NNJVILVZKWQKPM-UHFFFAOYSA-N Lidocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 description 1
- 235000006552 Liquidambar styraciflua Nutrition 0.000 description 1
- 229930045534 Me ester-Cyclohexaneundecanoic acid Natural products 0.000 description 1
- 244000246386 Mentha pulegium Species 0.000 description 1
- 235000016257 Mentha pulegium Nutrition 0.000 description 1
- 235000004357 Mentha x piperita Nutrition 0.000 description 1
- DUGOZIWVEXMGBE-UHFFFAOYSA-N Methylphenidate Chemical compound C=1C=CC=CC=1C(C(=O)OC)C1CCCCN1 DUGOZIWVEXMGBE-UHFFFAOYSA-N 0.000 description 1
- UEQUQVLFIPOEMF-UHFFFAOYSA-N Mianserin Chemical compound C1C2=CC=CC=C2N2CCN(C)CC2C2=CC=CC=C21 UEQUQVLFIPOEMF-UHFFFAOYSA-N 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 241001139947 Mida Species 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- VJGXOACAPIGNKO-UHFFFAOYSA-N N-(2,6-dichlorophenyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxamide Chemical compound ClC1=C(C(=CC=C1)Cl)NC(=O)N1C(C2=CC=CC=C2CC1)C VJGXOACAPIGNKO-UHFFFAOYSA-N 0.000 description 1
- IPNHPNIATOHDNN-GFCCVEGCSA-N N-[(1R)-2-[2-(2,6-dichlorophenyl)acetyl]-1-methyl-3,4-dihydro-1H-isoquinolin-5-yl]methanesulfonamide Chemical compound ClC1=C(C(=CC=C1)Cl)CC(=O)N1[C@@H](C2=CC=CC(=C2CC1)NS(=O)(=O)C)C IPNHPNIATOHDNN-GFCCVEGCSA-N 0.000 description 1
- YLXDSYKOBKBWJQ-LBPRGKRZSA-N N-[2-[(8S)-2,6,7,8-tetrahydro-1H-cyclopenta[e]benzofuran-8-yl]ethyl]propanamide Chemical compound C1=C2OCCC2=C2[C@H](CCNC(=O)CC)CCC2=C1 YLXDSYKOBKBWJQ-LBPRGKRZSA-N 0.000 description 1
- PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 description 1
- XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methylthiourea Natural products CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 description 1
- 101100030361 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pph-3 gene Proteins 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- CXOFVDLJLONNDW-UHFFFAOYSA-N Phenytoin Chemical compound N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 description 1
- XDXHAEQXIBQUEZ-UHFFFAOYSA-N Ropinirole hydrochloride Chemical compound Cl.CCCN(CCC)CCC1=CC=CC2=C1CC(=O)N2 XDXHAEQXIBQUEZ-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 102000004357 Transferases Human genes 0.000 description 1
- 108090000992 Transferases Proteins 0.000 description 1
- 229940123445 Tricyclic antidepressant Drugs 0.000 description 1
- OKJPEAGHQZHRQV-UHFFFAOYSA-N Triiodomethane Natural products IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical group [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 description 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 229960001138 acetylsalicylic acid Drugs 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 229960005305 adenosine Drugs 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001347 alkyl bromides Chemical class 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 1
- 229960004538 alprazolam Drugs 0.000 description 1
- VREFGVBLTWBCJP-UHFFFAOYSA-N alprazolam Chemical compound C12=CC(Cl)=CC=C2N2C(C)=NN=C2CN=C1C1=CC=CC=C1 VREFGVBLTWBCJP-UHFFFAOYSA-N 0.000 description 1
- WOLHOYHSEKDWQH-UHFFFAOYSA-N amantadine hydrochloride Chemical compound [Cl-].C1C(C2)CC3CC2CC1([NH3+])C3 WOLHOYHSEKDWQH-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229960000836 amitriptyline Drugs 0.000 description 1
- KRMDCWKBEZIMAB-UHFFFAOYSA-N amitriptyline Chemical compound C1CC2=CC=CC=C2C(=CCCN(C)C)C2=CC=CC=C21 KRMDCWKBEZIMAB-UHFFFAOYSA-N 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 229940025084 amphetamine Drugs 0.000 description 1
- 229940035676 analgesics Drugs 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 230000003288 anthiarrhythmic effect Effects 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000049 anti-anxiety effect Effects 0.000 description 1
- 230000003474 anti-emetic effect Effects 0.000 description 1
- 230000003561 anti-manic effect Effects 0.000 description 1
- 230000000648 anti-parkinson Effects 0.000 description 1
- 230000001663 anti-spastic effect Effects 0.000 description 1
- 239000003416 antiarrhythmic agent Substances 0.000 description 1
- 229940065524 anticholinergics inhalants for obstructive airway diseases Drugs 0.000 description 1
- 229940125681 anticonvulsant agent Drugs 0.000 description 1
- 239000001961 anticonvulsive agent Substances 0.000 description 1
- 229940125683 antiemetic agent Drugs 0.000 description 1
- 239000002111 antiemetic agent Substances 0.000 description 1
- 229940082988 antihypertensives serotonin antagonists Drugs 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000000939 antiparkinson agent Substances 0.000 description 1
- 239000003420 antiserotonin agent Substances 0.000 description 1
- 239000003443 antiviral agent Substances 0.000 description 1
- 229940121357 antivirals Drugs 0.000 description 1
- 239000002249 anxiolytic agent Substances 0.000 description 1
- 229940070343 apokyn Drugs 0.000 description 1
- 229960004046 apomorphine Drugs 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 229940039856 aricept Drugs 0.000 description 1
- 229960004372 aripiprazole Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- VHGCDTVCOLNTBX-QGZVFWFLSA-N atomoxetine Chemical compound O([C@H](CCNC)C=1C=CC=CC=1)C1=CC=CC=C1C VHGCDTVCOLNTBX-QGZVFWFLSA-N 0.000 description 1
- 229960002430 atomoxetine Drugs 0.000 description 1
- 125000004566 azetidin-1-yl group Chemical group N1(CCC1)* 0.000 description 1
- 229960000794 baclofen Drugs 0.000 description 1
- 239000003637 basic solution Substances 0.000 description 1
- 230000003542 behavioural effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- GIJXKZJWITVLHI-PMOLBWCYSA-N benzatropine Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(C=1C=CC=CC=1)C1=CC=CC=C1 GIJXKZJWITVLHI-PMOLBWCYSA-N 0.000 description 1
- 229960001081 benzatropine Drugs 0.000 description 1
- CPFJLLXFNPCTDW-BWSPSPBFSA-N benzatropine mesylate Chemical compound CS([O-])(=O)=O.O([C@H]1C[C@H]2CC[C@@H](C1)[NH+]2C)C(C=1C=CC=CC=1)C1=CC=CC=C1 CPFJLLXFNPCTDW-BWSPSPBFSA-N 0.000 description 1
- CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 1
- RROBIDXNTUAHFW-UHFFFAOYSA-N benzotriazol-1-yloxy-tris(dimethylamino)phosphanium Chemical compound C1=CC=C2N(O[P+](N(C)C)(N(C)C)N(C)C)N=NC2=C1 RROBIDXNTUAHFW-UHFFFAOYSA-N 0.000 description 1
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 229950009087 bifeprunox Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 238000012925 biological evaluation Methods 0.000 description 1
- HTJWUNNIRKDDIV-UHFFFAOYSA-N bis(1-adamantyl)-butylphosphane Chemical compound C1C(C2)CC(C3)CC2CC13P(CCCC)C1(C2)CC(C3)CC2CC3C1 HTJWUNNIRKDDIV-UHFFFAOYSA-N 0.000 description 1
- UORVGPXVDQYIDP-BJUDXGSMSA-N borane Chemical class [10BH3] UORVGPXVDQYIDP-BJUDXGSMSA-N 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 230000003491 cAMP production Effects 0.000 description 1
- 229960001948 caffeine Drugs 0.000 description 1
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 description 1
- 239000000480 calcium channel blocker Substances 0.000 description 1
- 229960002504 capsaicin Drugs 0.000 description 1
- 235000017663 capsaicin Nutrition 0.000 description 1
- FFGPTBGBLSHEPO-UHFFFAOYSA-N carbamazepine Chemical compound C1=CC2=CC=CC=C2N(C(=O)N)C2=CC=CC=C21 FFGPTBGBLSHEPO-UHFFFAOYSA-N 0.000 description 1
- 229960000623 carbamazepine Drugs 0.000 description 1
- 229960004205 carbidopa Drugs 0.000 description 1
- TZFNLOMSOLWIDK-JTQLQIEISA-N carbidopa (anhydrous) Chemical compound NN[C@@](C(O)=O)(C)CC1=CC=C(O)C(O)=C1 TZFNLOMSOLWIDK-JTQLQIEISA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 235000015218 chewing gum Nutrition 0.000 description 1
- ZPEIMTDSQAKGNT-UHFFFAOYSA-N chlorpromazine Chemical compound C1=C(Cl)C=C2N(CCCN(C)C)C3=CC=CC=C3SC2=C1 ZPEIMTDSQAKGNT-UHFFFAOYSA-N 0.000 description 1
- 229960001076 chlorpromazine Drugs 0.000 description 1
- 239000000812 cholinergic antagonist Substances 0.000 description 1
- 239000000544 cholinesterase inhibitor Substances 0.000 description 1
- 238000013375 chromatographic separation Methods 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 229960004606 clomipramine Drugs 0.000 description 1
- 229940097480 cogentin Drugs 0.000 description 1
- 230000019771 cognition Effects 0.000 description 1
- 230000003920 cognitive function Effects 0.000 description 1
- 229940075614 colloidal silicon dioxide Drugs 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000004590 computer program Methods 0.000 description 1
- 229940087613 comtan Drugs 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012004 corey–bakshi–shibata catalyst Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- NXQGGXCHGDYOHB-UHFFFAOYSA-L cyclopenta-1,4-dien-1-yl(diphenyl)phosphane;dichloropalladium;iron(2+) Chemical compound [Fe+2].Cl[Pd]Cl.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 NXQGGXCHGDYOHB-UHFFFAOYSA-L 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 239000012351 deprotecting agent Substances 0.000 description 1
- 238000010511 deprotection reaction Methods 0.000 description 1
- 238000000586 desensitisation Methods 0.000 description 1
- 229960000632 dexamfetamine Drugs 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- NIJJYAXOARWZEE-UHFFFAOYSA-N di-n-propyl-acetic acid Natural products CCCC(C(O)=O)CCC NIJJYAXOARWZEE-UHFFFAOYSA-N 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 125000005047 dihydroimidazolyl group Chemical group N1(CNC=C1)* 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 208000037765 diseases and disorders Diseases 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- ADEBPBSSDYVVLD-UHFFFAOYSA-N donepezil Natural products O=C1C=2C=C(OC)C(OC)=CC=2CC1CC(CC1)CCN1CC1=CC=CC=C1 ADEBPBSSDYVVLD-UHFFFAOYSA-N 0.000 description 1
- 229960003135 donepezil hydrochloride Drugs 0.000 description 1
- 239000000534 dopa decarboxylase inhibitor Substances 0.000 description 1
- 239000003136 dopamine receptor stimulating agent Substances 0.000 description 1
- 238000007876 drug discovery Methods 0.000 description 1
- 238000000132 electrospray ionisation Methods 0.000 description 1
- 229940071670 emsam Drugs 0.000 description 1
- 150000002085 enols Chemical class 0.000 description 1
- 229960003337 entacapone Drugs 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- GBBSUAFBMRNDJC-INIZCTEOSA-N eszopiclone Chemical compound C1CN(C)CCN1C(=O)O[C@H]1C2=NC=CN=C2C(=O)N1C1=CC=C(Cl)C=N1 GBBSUAFBMRNDJC-INIZCTEOSA-N 0.000 description 1
- 229960001578 eszopiclone Drugs 0.000 description 1
- DHLHPTWUARLUHM-UHFFFAOYSA-N ethyl 2-[1-(benzenesulfonyl)-5-chloroindol-4-yl]acetate Chemical compound C1(=CC=CC=C1)S(=O)(=O)N1C=CC2=C(C(=CC=C12)Cl)CC(=O)OCC DHLHPTWUARLUHM-UHFFFAOYSA-N 0.000 description 1
- IRSJDVYTJUCXRV-UHFFFAOYSA-N ethyl 2-bromo-2,2-difluoroacetate Chemical compound CCOC(=O)C(F)(F)Br IRSJDVYTJUCXRV-UHFFFAOYSA-N 0.000 description 1
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 125000006260 ethylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940108366 exelon Drugs 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229960002464 fluoxetine Drugs 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000007903 gelatin capsule Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229960003878 haloperidol Drugs 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000005554 hypnotics and sedatives Substances 0.000 description 1
- 230000036543 hypotension Effects 0.000 description 1
- 229960001680 ibuprofen Drugs 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 230000000155 isotopic effect Effects 0.000 description 1
- IQVRBWUUXZMOPW-PKNBQFBNSA-N istradefylline Chemical compound CN1C=2C(=O)N(CC)C(=O)N(CC)C=2N=C1\C=C\C1=CC=C(OC)C(OC)=C1 IQVRBWUUXZMOPW-PKNBQFBNSA-N 0.000 description 1
- 229950009028 istradefylline Drugs 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229960004502 levodopa Drugs 0.000 description 1
- 229960004194 lidocaine Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 239000003589 local anesthetic agent Substances 0.000 description 1
- 229960004391 lorazepam Drugs 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- VXWPONVCMVLXBW-UHFFFAOYSA-M magnesium;carbanide;iodide Chemical compound [CH3-].[Mg+2].[I-] VXWPONVCMVLXBW-UHFFFAOYSA-M 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- NTNUDYROPUKXNA-UHFFFAOYSA-N methyl 2-(triphenyl-$l^{5}-phosphanylidene)acetate Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=CC(=O)OC)C1=CC=CC=C1 NTNUDYROPUKXNA-UHFFFAOYSA-N 0.000 description 1
- YDCHPLOFQATIDS-UHFFFAOYSA-N methyl 2-bromoacetate Chemical compound COC(=O)CBr YDCHPLOFQATIDS-UHFFFAOYSA-N 0.000 description 1
- 125000006261 methyl amino sulfonyl group Chemical group [H]N(C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- CXHHBNMLPJOKQD-UHFFFAOYSA-M methyl carbonate Chemical compound COC([O-])=O CXHHBNMLPJOKQD-UHFFFAOYSA-M 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
- 229960001047 methyl salicylate Drugs 0.000 description 1
- NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 1
- 125000004458 methylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])[H] 0.000 description 1
- 239000012022 methylating agents Substances 0.000 description 1
- 230000001035 methylating effect Effects 0.000 description 1
- 229960001344 methylphenidate Drugs 0.000 description 1
- 229960003404 mexiletine Drugs 0.000 description 1
- 229960003955 mianserin Drugs 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229940101972 mirapex Drugs 0.000 description 1
- 229960001165 modafinil Drugs 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000004050 mood stabilizer Substances 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940033872 namenda Drugs 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000004081 narcotic agent Substances 0.000 description 1
- 229940020452 neupro Drugs 0.000 description 1
- 230000003705 neurological process Effects 0.000 description 1
- 210000002569 neuron Anatomy 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 239000002767 noradrenalin uptake inhibitor Substances 0.000 description 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
- 229940127221 norepinephrine reuptake inhibitor Drugs 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 229960005017 olanzapine Drugs 0.000 description 1
- KVWDHTXUZHCGIO-UHFFFAOYSA-N olanzapine Chemical compound C1CN(C)CCN1C1=NC2=CC=CC=C2NC2=C1C=C(C)S2 KVWDHTXUZHCGIO-UHFFFAOYSA-N 0.000 description 1
- 239000000014 opioid analgesic Substances 0.000 description 1
- 229940005483 opioid analgesics Drugs 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229960001057 paliperidone Drugs 0.000 description 1
- 229960005489 paracetamol Drugs 0.000 description 1
- 229940026768 parcopa Drugs 0.000 description 1
- 102000014187 peptide receptors Human genes 0.000 description 1
- 108010011903 peptide receptors Proteins 0.000 description 1
- 239000008177 pharmaceutical agent Substances 0.000 description 1
- 239000008024 pharmaceutical diluent Substances 0.000 description 1
- 150000002990 phenothiazines Chemical class 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
- 229960002036 phenytoin Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 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 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229940124606 potential therapeutic agent Drugs 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 229940002612 prodrug Drugs 0.000 description 1
- 239000000651 prodrug Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 125000003072 pyrazolidinyl group Chemical group 0.000 description 1
- 229960004431 quetiapine Drugs 0.000 description 1
- URKOMYMAXPYINW-UHFFFAOYSA-N quetiapine Chemical compound C1CN(CCOCCO)CCN1C1=NC2=CC=CC=C2SC2=CC=CC=C12 URKOMYMAXPYINW-UHFFFAOYSA-N 0.000 description 1
- 229960001150 ramelteon Drugs 0.000 description 1
- RUOKEQAAGRXIBM-GFCCVEGCSA-N rasagiline Chemical compound C1=CC=C2[C@H](NCC#C)CCC2=C1 RUOKEQAAGRXIBM-GFCCVEGCSA-N 0.000 description 1
- 229960000245 rasagiline Drugs 0.000 description 1
- 239000000018 receptor agonist Substances 0.000 description 1
- 229940044601 receptor agonist Drugs 0.000 description 1
- 229940044551 receptor antagonist Drugs 0.000 description 1
- 239000002464 receptor antagonist Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229940113775 requip Drugs 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 229960004136 rivastigmine Drugs 0.000 description 1
- 229960001879 ropinirole Drugs 0.000 description 1
- 229960003179 rotigotine Drugs 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 229960003946 selegiline Drugs 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229940001089 sinemet Drugs 0.000 description 1
- 238000009097 single-agent therapy Methods 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 229940001584 sodium metabisulfite Drugs 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 1
- 239000008259 solid foam Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000000527 sonication Methods 0.000 description 1
- 229940103422 stalevo Drugs 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 125000005555 sulfoximide group Chemical group 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 230000003956 synaptic plasticity Effects 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 229940000238 tasmar Drugs 0.000 description 1
- LQPZDJHBTUZFNB-XLLULAGJSA-N tert-butyl (1S)-1-methyl-5-(2,2,2-trifluoro-1-hydroxyethyl)-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound C[C@@H]1N(CCC2=C(C=CC=C12)C(C(F)(F)F)O)C(=O)OC(C)(C)C LQPZDJHBTUZFNB-XLLULAGJSA-N 0.000 description 1
- PUQJKWVPAWYSOU-NSHDSACASA-N tert-butyl (1S)-1-methyl-5-methylsulfanyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound C[C@@H]1N(CCC2=C(C=CC=C12)SC)C(=O)OC(C)(C)C PUQJKWVPAWYSOU-NSHDSACASA-N 0.000 description 1
- FNUQLSPFXBDGNI-VPHXOMNUSA-N tert-butyl (1S)-5-(2-amino-1-hydroxyethyl)-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound NCC(O)C1=C2CCN([C@H](C2=CC=C1)C)C(=O)OC(C)(C)C FNUQLSPFXBDGNI-VPHXOMNUSA-N 0.000 description 1
- XCBHHKQAWFCCNI-UHFFFAOYSA-N tert-butyl 1h-isoquinoline-2-carboxylate Chemical compound C1=CC=C2C=CN(C(=O)OC(C)(C)C)CC2=C1 XCBHHKQAWFCCNI-UHFFFAOYSA-N 0.000 description 1
- KKXRPHONDRYDRT-UHFFFAOYSA-N tert-butyl 5-amino-1-methyl-3,4-dihydro-1h-isoquinoline-2-carboxylate Chemical compound C1=CC=C2C(C)N(C(=O)OC(C)(C)C)CCC2=C1N KKXRPHONDRYDRT-UHFFFAOYSA-N 0.000 description 1
- YDHBUUMOFPRPNV-UHFFFAOYSA-N tert-butyl 5-azido-1-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylate Chemical compound N(=[N+]=[N-])C1=C2CCN(C(C2=CC=C1)C)C(=O)OC(C)(C)C YDHBUUMOFPRPNV-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- 125000000147 tetrahydroquinolinyl group Chemical class N1(CCCC2=CC=CC=C12)* 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- MIQPIUSUKVNLNT-UHFFFAOYSA-N tolcapone Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC(O)=C(O)C([N+]([O-])=O)=C1 MIQPIUSUKVNLNT-UHFFFAOYSA-N 0.000 description 1
- 229960004603 tolcapone Drugs 0.000 description 1
- PHLBKPHSAVXXEF-UHFFFAOYSA-N trazodone Chemical compound ClC1=CC=CC(N2CCN(CCCN3C(N4C=CC=CC4=N3)=O)CC2)=C1 PHLBKPHSAVXXEF-UHFFFAOYSA-N 0.000 description 1
- 229960003991 trazodone Drugs 0.000 description 1
- 239000003029 tricyclic antidepressant agent Substances 0.000 description 1
- KIEXGUUJAYEUSM-UHFFFAOYSA-N trifluoromethylsilane Chemical compound FC(F)(F)[SiH3] KIEXGUUJAYEUSM-UHFFFAOYSA-N 0.000 description 1
- MWKJTNBSKNUMFN-UHFFFAOYSA-N trifluoromethyltrimethylsilane Chemical compound C[Si](C)(C)C(F)(F)F MWKJTNBSKNUMFN-UHFFFAOYSA-N 0.000 description 1
- 125000004953 trihalomethyl group Chemical group 0.000 description 1
- UCPYLLCMEDAXFR-UHFFFAOYSA-N triphosgene Chemical compound ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl UCPYLLCMEDAXFR-UHFFFAOYSA-N 0.000 description 1
- BWHDROKFUHTORW-UHFFFAOYSA-N tritert-butylphosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(C)(C)C BWHDROKFUHTORW-UHFFFAOYSA-N 0.000 description 1
- 125000005500 uronium group Chemical group 0.000 description 1
- MSRILKIQRXUYCT-UHFFFAOYSA-M valproate semisodium Chemical compound [Na+].CCCC(C(O)=O)CCC.CCCC(C([O-])=O)CCC MSRILKIQRXUYCT-UHFFFAOYSA-M 0.000 description 1
- 229960000604 valproic acid Drugs 0.000 description 1
- 239000008215 water for injection Substances 0.000 description 1
- 229940068543 zelapar Drugs 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229960000607 ziprasidone Drugs 0.000 description 1
- MVWVFYHBGMAFLY-UHFFFAOYSA-N ziprasidone Chemical compound C1=CC=C2C(N3CCN(CC3)CCC3=CC=4CC(=O)NC=4C=C3Cl)=NSC2=C1 MVWVFYHBGMAFLY-UHFFFAOYSA-N 0.000 description 1
- ZAFYATHCZYHLPB-UHFFFAOYSA-N zolpidem Chemical compound N1=C2C=CC(C)=CN2C(CC(=O)N(C)C)=C1C1=CC=C(C)C=C1 ZAFYATHCZYHLPB-UHFFFAOYSA-N 0.000 description 1
- 229960001475 zolpidem Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
- C07D217/06—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with the ring nitrogen atom acylated by carboxylic or carbonic acids, or with sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Epidemiology (AREA)
- Addiction (AREA)
- Hospice & Palliative Care (AREA)
- Anesthesiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14188174 | 2014-10-08 | ||
| PCT/EP2015/073053 WO2016055479A1 (en) | 2014-10-08 | 2015-10-06 | Tetrahydroisoquinoline derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2821821T3 true ES2821821T3 (es) | 2021-04-27 |
Family
ID=51790569
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES15775688T Active ES2821821T3 (es) | 2014-10-08 | 2015-10-06 | Derivados de tetrahidroisoquinolina |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US10105359B2 (enExample) |
| EP (1) | EP3204359B1 (enExample) |
| JP (1) | JP6622299B2 (enExample) |
| CN (1) | CN107001278B (enExample) |
| BR (1) | BR112017007123B1 (enExample) |
| CA (1) | CA2963951C (enExample) |
| CY (1) | CY1123417T1 (enExample) |
| DK (1) | DK3204359T3 (enExample) |
| EA (1) | EA035544B1 (enExample) |
| ES (1) | ES2821821T3 (enExample) |
| HR (1) | HRP20201469T1 (enExample) |
| HU (1) | HUE050664T2 (enExample) |
| LT (1) | LT3204359T (enExample) |
| PL (1) | PL3204359T3 (enExample) |
| PT (1) | PT3204359T (enExample) |
| RS (1) | RS60933B1 (enExample) |
| SI (1) | SI3204359T1 (enExample) |
| WO (1) | WO2016055479A1 (enExample) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA3012560A1 (en) * | 2016-02-25 | 2017-08-31 | Asceneuron S.A. | Glycosidase inhibitors |
| JP6908623B2 (ja) * | 2016-04-13 | 2021-07-28 | ユーシービー バイオファルマ エスアールエル | テトラヒドロイソキノリン誘導体 |
| CN107698433A (zh) * | 2017-09-12 | 2018-02-16 | 潍坊滨海石油化工有限公司 | 苯乙酸的制备方法 |
| EA202091323A1 (ru) | 2017-12-01 | 2020-10-09 | Юсб Байофарма Срл | Визуализирующие средства |
| TWI725408B (zh) * | 2018-04-20 | 2021-04-21 | 美商美國禮來大藥廠 | 多巴胺d1受體正向異位調節劑 |
| CN114008032B (zh) * | 2019-07-01 | 2023-11-10 | Ucb生物制药有限责任公司 | 作为d1正变构调节剂的取代的四氢异喹啉衍生物 |
| AU2020299953B2 (en) * | 2019-07-01 | 2025-06-05 | UCB Biopharma SRL | A substituted tetrahydroisoquinoline derivative as a D1 positive allosteric modulator |
| CN115916338A (zh) * | 2020-04-24 | 2023-04-04 | 加利福尼亚大学董事会 | Nurr1受体调节剂及其用途 |
| CN111943930B (zh) * | 2020-08-25 | 2022-11-01 | 南京三元阳普医药科技有限公司 | Lasmiditan的合成工艺 |
| DK4200280T3 (da) * | 2020-10-07 | 2024-03-04 | Lilly Co Eli | Phenyl-3,4-dihydroisoquinolin-2(1H)-yl-ethan-on-derivater som positive allosteriske modulatorer af dopamin-D1-receptorer |
| WO2022117678A1 (en) | 2020-12-03 | 2022-06-09 | UCB Biopharma SRL | Octahydroisoquinolinyl derivatives |
| US20240083875A1 (en) | 2020-12-18 | 2024-03-14 | UCB Biopharma SRL | Dihydroisoquinolinyl derivatives |
| CN116601161A (zh) * | 2020-12-18 | 2023-08-15 | Ucb生物制药有限责任公司 | 2-(3,5-二氯-1-甲基-吲唑-4-基)-1-[(1s,3r)-3-(羟基甲基)-5-(1-羟基-1-甲基-乙基)-1-甲基-3,4-二氢-1h-异喹啉-2-基]乙酮的前药 |
| US20240000769A1 (en) * | 2020-12-18 | 2024-01-04 | UCB Biopharma SRL | Amorphous solid dispersions |
| PL4263517T3 (pl) * | 2020-12-18 | 2025-03-31 | UCB Biopharma SRL | Podstawiona pochodna tetrahydroizochinoliny jako pozytywny modulator allosteryczny d1 |
| AU2022234744B2 (en) | 2021-03-08 | 2025-06-26 | Eli Lilly And Company | Use of mevidalen and other d1 positive allosteric modulators in the treatment of hallucinations and dementia-related psychosis |
| CN117337173A (zh) | 2021-03-09 | 2024-01-02 | 伊莱利利公司 | 美维达林和其他d1正向别构调节剂用于减缓帕金森氏病进展的用途 |
| CN114671810B (zh) * | 2022-03-21 | 2024-03-22 | 济南鸿湾生物技术有限公司 | 一种咪唑苯脲的制备方法 |
| CN115611768B (zh) * | 2022-11-14 | 2024-03-05 | 郑州大学 | 一种3,4-二氯苯腈的合成方法 |
| CN118724764B (zh) * | 2024-06-07 | 2025-11-18 | 绍兴文理学院 | 一种芳基伯磺酰胺类化合物的制备方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4766131A (en) * | 1980-10-17 | 1988-08-23 | Pennwalt Corporation | 2-amino (or hydroxy) phenethyl-1,2,3,4-tetrahydroisoquinolines as analgesics |
| MXPA04005988A (es) * | 2001-12-19 | 2004-09-27 | Lundbeck & Co As H | 3,4-dihidro-1h-isoquinolin-2-il-derivados. |
| JP4685861B2 (ja) * | 2004-04-29 | 2011-05-18 | アベンティス・ファーマスーティカルズ・インコーポレイテツド | ドーパミンアゴニストとしての3−ピペリジニルイソクロマン−5−オール |
| MX2009009415A (es) * | 2007-03-01 | 2009-09-11 | Janssen Pharmaceutica Nv | Compuestos de tetrahidroisoquinolina como moduladores del receptor h3 de la histamina. |
-
2015
- 2015-10-06 LT LTEP15775688.3T patent/LT3204359T/lt unknown
- 2015-10-06 HU HUE15775688A patent/HUE050664T2/hu unknown
- 2015-10-06 EP EP15775688.3A patent/EP3204359B1/en active Active
- 2015-10-06 PL PL15775688.3T patent/PL3204359T3/pl unknown
- 2015-10-06 HR HRP20201469TT patent/HRP20201469T1/hr unknown
- 2015-10-06 DK DK15775688.3T patent/DK3204359T3/da active
- 2015-10-06 EA EA201790785A patent/EA035544B1/ru not_active IP Right Cessation
- 2015-10-06 RS RS20201139A patent/RS60933B1/sr unknown
- 2015-10-06 CN CN201580064005.3A patent/CN107001278B/zh not_active Expired - Fee Related
- 2015-10-06 US US15/517,795 patent/US10105359B2/en active Active
- 2015-10-06 PT PT157756883T patent/PT3204359T/pt unknown
- 2015-10-06 CA CA2963951A patent/CA2963951C/en active Active
- 2015-10-06 JP JP2017518989A patent/JP6622299B2/ja active Active
- 2015-10-06 SI SI201531348T patent/SI3204359T1/sl unknown
- 2015-10-06 BR BR112017007123-1A patent/BR112017007123B1/pt not_active IP Right Cessation
- 2015-10-06 WO PCT/EP2015/073053 patent/WO2016055479A1/en not_active Ceased
- 2015-10-06 ES ES15775688T patent/ES2821821T3/es active Active
-
2020
- 2020-09-30 CY CY20201100923T patent/CY1123417T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| RS60933B1 (sr) | 2020-11-30 |
| EA201790785A1 (ru) | 2017-10-31 |
| US10105359B2 (en) | 2018-10-23 |
| LT3204359T (lt) | 2020-10-12 |
| CA2963951C (en) | 2023-02-28 |
| HRP20201469T1 (hr) | 2020-12-11 |
| BR112017007123B1 (pt) | 2023-01-31 |
| BR112017007123A2 (pt) | 2017-12-19 |
| WO2016055479A1 (en) | 2016-04-14 |
| DK3204359T3 (da) | 2020-09-14 |
| PL3204359T3 (pl) | 2021-03-22 |
| EA035544B1 (ru) | 2020-07-03 |
| EP3204359A1 (en) | 2017-08-16 |
| HUE050664T2 (hu) | 2020-12-28 |
| CA2963951A1 (en) | 2016-04-14 |
| JP2017530185A (ja) | 2017-10-12 |
| PT3204359T (pt) | 2020-09-24 |
| CN107001278B (zh) | 2020-11-24 |
| CN107001278A (zh) | 2017-08-01 |
| CY1123417T1 (el) | 2021-12-31 |
| SI3204359T1 (sl) | 2020-10-30 |
| EP3204359B1 (en) | 2020-07-01 |
| US20170304292A1 (en) | 2017-10-26 |
| JP6622299B2 (ja) | 2019-12-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2821821T3 (es) | Derivados de tetrahidroisoquinolina | |
| ES2955037T3 (es) | Nuevos compuestos heterocíclicos | |
| CN109715613B (zh) | 杂环化合物 | |
| CN113214287B (zh) | Hpk1抑制剂及其使用方法 | |
| JP6529085B2 (ja) | 複素環化合物 | |
| BR112021008986A2 (pt) | composto, composto da fórmula, composto ou sal farmaceuticamente aceitável, composição farmacêutica, métodos para tratar o câncer, para regular a atividade de uma proteína mutante g12c k-ras, para inibir a proliferação de uma população de células, para tratar um distúrbio mediado, para preparar uma proteína e para inibir metástase de tumor e uso | |
| JP2022515879A (ja) | 複素環式化合物、中間体、その製造方法及び応用 本願は、出願日が2018年12月29日の中国特許出願cn 201811642319、出願日が2019年05月24日の中国特許出願cn201910440214.3及び出願日が2019年10月24日の中国特許出願cn201911016158.7に基づいて優先権を主張する。また、上記中国特許出願の全文は本願に援用される。 | |
| JP2022516469A (ja) | ユビキチン特異的プロテアーゼ1を阻害するための組成物 | |
| TW201710255A (zh) | 雜環化合物 | |
| EA021126B1 (ru) | Замещенные изохинолиноны и хинализолиноны | |
| BR112017023147B1 (pt) | Derivados de azabenzimidazóis, seus usos como moduladores do receptor de ampa e composições farmacêuticas | |
| JPWO2017069173A1 (ja) | 複素環化合物 | |
| CN105745209A (zh) | 三唑并吡啶化合物、组合物及其使用方法 | |
| CN112334450A (zh) | 作为RORγt的调节剂的苯基和吡啶基取代的咪唑 | |
| ES2960408T3 (es) | Compuesto heterocíclico y su uso como modulador alostérico positivo del receptor M1 muscarínico colinérgico | |
| JP2022540825A (ja) | Mcl-1阻害剤としての大環状スピロ環誘導体 | |
| WO2019189555A1 (ja) | 複素環化合物 | |
| ES2729490T3 (es) | Derivados de isoindolina | |
| JP2022544700A (ja) | 筋萎縮性側索硬化症および関連障害の治療のためにtdp-43に結合する分子 | |
| CN114555573A (zh) | 前列腺素e2(pge2)ep4受体拮抗剂 | |
| ES3001126T3 (es) | Derivados de 1-((1H-pirazol-4-il)metil)-3-(fenil)-1,3-dihidro-2H-imidazol-2-ona y compuestos relacionados como antagonistas de GPR139 para el tratamiento de la depresión | |
| BR112019026096A2 (pt) | composto, medicamento, métodos para modulação alostérica positiva do receptor muscarínico colinérgico m1 e para a profilaxia ou o tratamento de constipação, e, uso do composto | |
| RU2809257C2 (ru) | Новые гетероциклические соединения | |
| HK40057478B (zh) | Hpk1抑制剂及其使用方法 | |
| KR20230104163A (ko) | 암 치료용 벤조[h]퀴나졸린-4-아민 및 티에노[3,2-h]퀴나졸린-4-아민 유도체 |