JP2010509334A5 - - Google Patents
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- JP2010509334A5 JP2010509334A5 JP2009536293A JP2009536293A JP2010509334A5 JP 2010509334 A5 JP2010509334 A5 JP 2010509334A5 JP 2009536293 A JP2009536293 A JP 2009536293A JP 2009536293 A JP2009536293 A JP 2009536293A JP 2010509334 A5 JP2010509334 A5 JP 2010509334A5
- Authority
- JP
- Japan
- Prior art keywords
- amine
- hexane
- alkyl
- bicyclo
- dichlorophenyl
- 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.)
- Pending
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- 125000000217 alkyl group Chemical group 0.000 claims 64
- 150000001875 compounds Chemical class 0.000 claims 50
- 125000003545 alkoxy group Chemical group 0.000 claims 47
- 125000000304 alkynyl group Chemical group 0.000 claims 24
- 125000004093 cyano group Chemical group *C#N 0.000 claims 24
- 229910052736 halogen Inorganic materials 0.000 claims 24
- 125000005843 halogen group Chemical group 0.000 claims 24
- 238000000034 method Methods 0.000 claims 24
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 16
- 125000003342 alkenyl group Chemical group 0.000 claims 16
- 125000003282 alkyl amino group Chemical group 0.000 claims 16
- 125000004104 aryloxy group Chemical group 0.000 claims 16
- 150000002367 halogens Chemical class 0.000 claims 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 16
- 125000001424 substituent group Chemical group 0.000 claims 16
- 229910052739 hydrogen Inorganic materials 0.000 claims 15
- 239000001257 hydrogen Substances 0.000 claims 15
- 125000003118 aryl group Chemical group 0.000 claims 14
- -1 chloro, bromo, iodo Chemical group 0.000 claims 13
- 150000002431 hydrogen Chemical class 0.000 claims 10
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 claims 9
- 125000001624 naphthyl group Chemical group 0.000 claims 9
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims 8
- 125000001589 carboacyl group Chemical group 0.000 claims 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 8
- 125000001153 fluoro group Chemical group F* 0.000 claims 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 8
- 125000004438 haloalkoxy group Chemical group 0.000 claims 7
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- HQLZFBUAULNEGP-UHFFFAOYSA-N hexan-3-amine Chemical compound CCCC(N)CC HQLZFBUAULNEGP-UHFFFAOYSA-N 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 7
- 210000003169 central nervous system Anatomy 0.000 claims 6
- 208000015114 central nervous system disease Diseases 0.000 claims 6
- 238000006243 chemical reaction Methods 0.000 claims 6
- 230000007062 hydrolysis Effects 0.000 claims 6
- 238000006460 hydrolysis reaction Methods 0.000 claims 6
- 239000012453 solvate Substances 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- WGBBUURBHXLGFM-UHFFFAOYSA-N hexan-2-amine Chemical compound CCCCC(C)N WGBBUURBHXLGFM-UHFFFAOYSA-N 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- 239000000651 prodrug Substances 0.000 claims 5
- 229940002612 prodrug Drugs 0.000 claims 5
- 150000001412 amines Chemical class 0.000 claims 4
- 238000005888 cyclopropanation reaction Methods 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- CYWNXJDAHXCTDY-UHFFFAOYSA-N n,n-dimethyl-1-naphthalen-1-ylbicyclo[3.1.0]hexan-3-amine Chemical compound C1=CC=C2C(C34CC3CC(C4)N(C)C)=CC=CC2=C1 CYWNXJDAHXCTDY-UHFFFAOYSA-N 0.000 claims 4
- BJHKEGAQSFMVQE-UHFFFAOYSA-N n-methyl-1-naphthalen-1-ylbicyclo[3.1.0]hexan-3-amine Chemical compound C1=CC=C2C(C34CC3CC(C4)NC)=CC=CC2=C1 BJHKEGAQSFMVQE-UHFFFAOYSA-N 0.000 claims 4
- GTAVXMAPXFMUMZ-UHFFFAOYSA-N n-methyl-1-naphthalen-2-ylbicyclo[3.1.0]hexan-3-amine Chemical compound C1=CC=CC2=CC(C34CC3CC(C4)NC)=CC=C21 GTAVXMAPXFMUMZ-UHFFFAOYSA-N 0.000 claims 4
- JZLBUIIHIYKZQA-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-n,n-dimethylbicyclo[3.1.0]hexan-2-amine Chemical compound CN(C)C1CCC2CC12C1=CC=C(Cl)C(Cl)=C1 JZLBUIIHIYKZQA-UHFFFAOYSA-N 0.000 claims 3
- WAEQWTAGGVBEBY-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-n-methylbicyclo[3.1.0]hexan-2-amine Chemical compound CNC1CCC2CC12C1=CC=C(Cl)C(Cl)=C1 WAEQWTAGGVBEBY-UHFFFAOYSA-N 0.000 claims 3
- AKSYYBWFPSRFMM-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)bicyclo[3.1.0]hexan-2-amine Chemical compound NC1CCC2CC12C1=CC=C(Cl)C(Cl)=C1 AKSYYBWFPSRFMM-UHFFFAOYSA-N 0.000 claims 3
- BOPSAQVEGQKJPU-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)bicyclo[3.1.0]hexan-3-amine Chemical compound C1C(N)CC2CC21C1=CC=C(Cl)C(Cl)=C1 BOPSAQVEGQKJPU-UHFFFAOYSA-N 0.000 claims 3
- 208000019901 Anxiety disease Diseases 0.000 claims 3
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims 3
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims 3
- 239000003638 chemical reducing agent Substances 0.000 claims 3
- 239000003795 chemical substances by application Substances 0.000 claims 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 3
- 239000003937 drug carrier Substances 0.000 claims 3
- 230000002140 halogenating effect Effects 0.000 claims 3
- 230000026030 halogenation Effects 0.000 claims 3
- 238000005658 halogenation reaction Methods 0.000 claims 3
- 208000035231 inattentive type attention deficit hyperactivity disease Diseases 0.000 claims 3
- DWRTZTKSEPTGOG-UHFFFAOYSA-N n,n-dimethyl-1-(4-methylphenyl)bicyclo[3.1.0]hexan-2-amine Chemical compound CN(C)C1CCC2CC12C1=CC=C(C)C=C1 DWRTZTKSEPTGOG-UHFFFAOYSA-N 0.000 claims 3
- BWDGXSGYSZASAX-UHFFFAOYSA-N n,n-dimethyl-1-naphthalen-1-ylbicyclo[3.1.0]hexan-4-amine Chemical compound C1=CC=C2C(C34CCC(C3C4)N(C)C)=CC=CC2=C1 BWDGXSGYSZASAX-UHFFFAOYSA-N 0.000 claims 3
- OUFATBSGEBXXAP-UHFFFAOYSA-N n-methyl-1-(4-methylphenyl)bicyclo[3.1.0]hexan-3-amine Chemical compound C1C(NC)CC2CC21C1=CC=C(C)C=C1 OUFATBSGEBXXAP-UHFFFAOYSA-N 0.000 claims 3
- WMEPENWGXQHPML-UHFFFAOYSA-N n-methyl-1-(4-methylphenyl)bicyclo[3.1.0]hexan-4-amine Chemical compound C1C2C(NC)CCC21C1=CC=C(C)C=C1 WMEPENWGXQHPML-UHFFFAOYSA-N 0.000 claims 3
- NOHMVCZNSGEVCK-UHFFFAOYSA-N n-methyl-1-naphthalen-1-ylbicyclo[3.1.0]hexan-4-amine Chemical compound C1=CC=C2C(C34CCC(C3C4)NC)=CC=CC2=C1 NOHMVCZNSGEVCK-UHFFFAOYSA-N 0.000 claims 3
- GPDDOMZRRYENNX-UHFFFAOYSA-N n-methyl-1-naphthalen-2-ylbicyclo[3.1.0]hexan-4-amine Chemical compound C1=CC=CC2=CC(C34CCC(C3C4)NC)=CC=C21 GPDDOMZRRYENNX-UHFFFAOYSA-N 0.000 claims 3
- 238000006722 reduction reaction Methods 0.000 claims 3
- 238000006268 reductive amination reaction Methods 0.000 claims 3
- 238000007363 ring formation reaction Methods 0.000 claims 3
- 208000024891 symptom Diseases 0.000 claims 3
- BOPSAQVEGQKJPU-AUTRQRHGSA-N (1r,3s,5r)-1-(3,4-dichlorophenyl)bicyclo[3.1.0]hexan-3-amine Chemical compound C1([C@@]23C[C@@H]2C[C@@H](C3)N)=CC=C(Cl)C(Cl)=C1 BOPSAQVEGQKJPU-AUTRQRHGSA-N 0.000 claims 2
- QOERHOWUEYOSMZ-HEHGZKQESA-N (1r,3s,5r)-1-naphthalen-1-ylbicyclo[3.1.0]hexan-3-amine Chemical compound C1=CC=C2C([C@@]34C[C@@H]3C[C@@H](C4)N)=CC=CC2=C1 QOERHOWUEYOSMZ-HEHGZKQESA-N 0.000 claims 2
- QOERHOWUEYOSMZ-GMRULEOSSA-N (1r,5r)-1-naphthalen-1-ylbicyclo[3.1.0]hexan-3-amine Chemical compound C1=CC=C2C([C@@]34C[C@@H]3CC(C4)N)=CC=CC2=C1 QOERHOWUEYOSMZ-GMRULEOSSA-N 0.000 claims 2
- ZALDYBSAVFVVJR-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-n,n-dimethylbicyclo[3.1.0]hexan-4-amine Chemical compound C1C2C(N(C)C)CCC21C1=CC=C(Cl)C(Cl)=C1 ZALDYBSAVFVVJR-UHFFFAOYSA-N 0.000 claims 2
- MIOACJKLZCNKBE-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-n-methylbicyclo[3.1.0]hexan-3-amine Chemical compound C1C(NC)CC2CC21C1=CC=C(Cl)C(Cl)=C1 MIOACJKLZCNKBE-UHFFFAOYSA-N 0.000 claims 2
- VRJQNBKWKVEZJL-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-n-methylbicyclo[3.1.0]hexan-4-amine Chemical compound C1C2C(NC)CCC21C1=CC=C(Cl)C(Cl)=C1 VRJQNBKWKVEZJL-UHFFFAOYSA-N 0.000 claims 2
- KCYNWEONSBNBPP-UHFFFAOYSA-N 1-(4-methylphenyl)bicyclo[3.1.0]hexan-2-amine Chemical compound C1=CC(C)=CC=C1C1(C(CC2)N)C2C1 KCYNWEONSBNBPP-UHFFFAOYSA-N 0.000 claims 2
- ZIHMRFCEZLROBE-UHFFFAOYSA-N 1-(4-methylphenyl)bicyclo[3.1.0]hexan-4-amine Chemical compound C1=CC(C)=CC=C1C1(CCC2N)C2C1 ZIHMRFCEZLROBE-UHFFFAOYSA-N 0.000 claims 2
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims 2
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims 2
- PVXPMXRWNGMGRF-UHFFFAOYSA-N bicyclo[3.1.0]hexan-2-amine Chemical compound NC1CCC2CC12 PVXPMXRWNGMGRF-UHFFFAOYSA-N 0.000 claims 2
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- GQJJTPIKRQRPGE-UHFFFAOYSA-N n,n-dimethyl-1-(4-methylphenyl)bicyclo[3.1.0]hexan-3-amine Chemical compound C1C(N(C)C)CC2CC21C1=CC=C(C)C=C1 GQJJTPIKRQRPGE-UHFFFAOYSA-N 0.000 claims 2
- IOGUNWAJSSFGTM-UHFFFAOYSA-N n,n-dimethyl-1-(4-methylphenyl)bicyclo[3.1.0]hexan-4-amine Chemical compound C1C2C(N(C)C)CCC21C1=CC=C(C)C=C1 IOGUNWAJSSFGTM-UHFFFAOYSA-N 0.000 claims 2
- IQAWRFUHTQGEFO-UHFFFAOYSA-N n-methyl-1-(4-methylphenyl)bicyclo[3.1.0]hexan-2-amine Chemical compound CNC1CCC2CC12C1=CC=C(C)C=C1 IQAWRFUHTQGEFO-UHFFFAOYSA-N 0.000 claims 2
- 230000001590 oxidative effect Effects 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 claims 2
- 238000000926 separation method Methods 0.000 claims 2
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 claims 2
- 239000003981 vehicle Substances 0.000 claims 2
- SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 claims 1
- BOPSAQVEGQKJPU-SBMIAAHKSA-N (1r,3r,5r)-1-(3,4-dichlorophenyl)bicyclo[3.1.0]hexan-3-amine Chemical compound C1([C@@]23C[C@@H]2C[C@H](C3)N)=CC=C(Cl)C(Cl)=C1 BOPSAQVEGQKJPU-SBMIAAHKSA-N 0.000 claims 1
- QOERHOWUEYOSMZ-WOSRLPQWSA-N (1r,3r,5r)-1-naphthalen-1-ylbicyclo[3.1.0]hexan-3-amine Chemical compound C1=CC=C2C([C@@]34C[C@@H]3C[C@H](C4)N)=CC=CC2=C1 QOERHOWUEYOSMZ-WOSRLPQWSA-N 0.000 claims 1
- BOPSAQVEGQKJPU-OYGLUPDLSA-N (1r,5r)-1-(3,4-dichlorophenyl)bicyclo[3.1.0]hexan-3-amine Chemical compound C1([C@@]23C[C@@H]2CC(C3)N)=CC=C(Cl)C(Cl)=C1 BOPSAQVEGQKJPU-OYGLUPDLSA-N 0.000 claims 1
- BOPSAQVEGQKJPU-YKXYSFTHSA-N (1s,5s)-1-(3,4-dichlorophenyl)bicyclo[3.1.0]hexan-3-amine Chemical compound C1([C@]23C[C@H]2CC(C3)N)=CC=C(Cl)C(Cl)=C1 BOPSAQVEGQKJPU-YKXYSFTHSA-N 0.000 claims 1
- QOERHOWUEYOSMZ-LRRQEPCHSA-N (1s,5s)-1-naphthalen-1-ylbicyclo[3.1.0]hexan-3-amine Chemical compound C1=CC=C2C([C@]34C[C@H]3CC(C4)N)=CC=CC2=C1 QOERHOWUEYOSMZ-LRRQEPCHSA-N 0.000 claims 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 1
- XIBILYUXEMBUGY-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-n,n-dimethylbicyclo[3.1.0]hexan-3-amine Chemical compound C1C(N(C)C)CC2CC21C1=CC=C(Cl)C(Cl)=C1 XIBILYUXEMBUGY-UHFFFAOYSA-N 0.000 claims 1
- DKBYLKRWTWSWJM-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)bicyclo[3.1.0]hexan-4-amine Chemical compound C1C2C(N)CCC21C1=CC=C(Cl)C(Cl)=C1 DKBYLKRWTWSWJM-UHFFFAOYSA-N 0.000 claims 1
- NRBMWIVJOBMUPX-UHFFFAOYSA-N 1-(4-methylphenyl)bicyclo[3.1.0]hexan-3-amine Chemical compound C1=CC(C)=CC=C1C1(CC(N)C2)C2C1 NRBMWIVJOBMUPX-UHFFFAOYSA-N 0.000 claims 1
- DTWCFCILAJVNPE-UHFFFAOYSA-N 3-methoxycyclopent-2-en-1-one Chemical compound COC1=CC(=O)CC1 DTWCFCILAJVNPE-UHFFFAOYSA-N 0.000 claims 1
- 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 claims 1
- YUOQNYSTGJUYGJ-UHFFFAOYSA-N CC1(CCC2C1(C2)C)N Chemical compound CC1(CCC2C1(C2)C)N YUOQNYSTGJUYGJ-UHFFFAOYSA-N 0.000 claims 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims 1
- HAEHSFVDBQNHOX-UHFFFAOYSA-N bicyclo[3.1.0]hexan-3-amine Chemical compound C1C(N)CC2CC21 HAEHSFVDBQNHOX-UHFFFAOYSA-N 0.000 claims 1
- 230000000035 biogenic effect Effects 0.000 claims 1
- 230000031709 bromination Effects 0.000 claims 1
- 238000005893 bromination reaction Methods 0.000 claims 1
- 230000004700 cellular uptake Effects 0.000 claims 1
- 229960003638 dopamine Drugs 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 150000004677 hydrates Chemical class 0.000 claims 1
- 230000003834 intracellular effect Effects 0.000 claims 1
- 210000004962 mammalian cell Anatomy 0.000 claims 1
- 239000002858 neurotransmitter agent Substances 0.000 claims 1
- 229960002748 norepinephrine Drugs 0.000 claims 1
- SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 claims 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 230000002829 reductive effect Effects 0.000 claims 1
- 229940076279 serotonin Drugs 0.000 claims 1
- 0 CC(C1(*)C(*)C(*)C2*)C12[Al] Chemical compound CC(C1(*)C(*)C(*)C2*)C12[Al] 0.000 description 11
- KKNFDVOWVMDKSH-UHFFFAOYSA-N N#CC1(C(CO)C1)[AlH2] Chemical compound N#CC1(C(CO)C1)[AlH2] KKNFDVOWVMDKSH-UHFFFAOYSA-N 0.000 description 4
- QBVKKIOYIGJWPE-UHFFFAOYSA-N O=C(CC1C2)CC12[AlH2] Chemical compound O=C(CC1C2)CC12[AlH2] QBVKKIOYIGJWPE-UHFFFAOYSA-N 0.000 description 4
- XBGGZYQBIQAYII-UHFFFAOYSA-N CSCS(c1ccccc1)(=O)=O Chemical compound CSCS(c1ccccc1)(=O)=O XBGGZYQBIQAYII-UHFFFAOYSA-N 0.000 description 2
- WTRGSJZKMXRUAN-UHFFFAOYSA-N O=C(CC1)C=C1[AlH2] Chemical compound O=C(CC1)C=C1[AlH2] WTRGSJZKMXRUAN-UHFFFAOYSA-N 0.000 description 2
- ZKYGYYQFDBLDTA-UHFFFAOYSA-N [AlH2]C1(CBr)C(CBr)C1 Chemical compound [AlH2]C1(CBr)C(CBr)C1 ZKYGYYQFDBLDTA-UHFFFAOYSA-N 0.000 description 2
- QGIRJOZKFABRQW-UHFFFAOYSA-N CSC(CC1C2)(C[C@]12[AlH2])C(C(c1ccccc1)=O)=O Chemical compound CSC(CC1C2)(C[C@]12[AlH2])C(C(c1ccccc1)=O)=O QGIRJOZKFABRQW-UHFFFAOYSA-N 0.000 description 1
- YRFBEHLXLHSHMV-BRJRFNKRSA-N N#CC1[C@@H](CO)C1 Chemical compound N#CC1[C@@H](CO)C1 YRFBEHLXLHSHMV-BRJRFNKRSA-N 0.000 description 1
- YRFBEHLXLHSHMV-RFZPGFLSSA-N N#C[C@@H]1[C@@H](CO)C1 Chemical compound N#C[C@@H]1[C@@H](CO)C1 YRFBEHLXLHSHMV-RFZPGFLSSA-N 0.000 description 1
- GTRJVJIYBULAFO-UHFFFAOYSA-N N=C1OCC(C2)C12[AlH2] Chemical compound N=C1OCC(C2)C12[AlH2] GTRJVJIYBULAFO-UHFFFAOYSA-N 0.000 description 1
- JKBHGPZVUHEWGP-UHFFFAOYSA-N O=C(CC1)C(C2)C12[AlH2] Chemical compound O=C(CC1)C(C2)C12[AlH2] JKBHGPZVUHEWGP-UHFFFAOYSA-N 0.000 description 1
- IQDJKWJLZKSMGB-UHFFFAOYSA-N O=C(CCC1C2)C12[AlH2] Chemical compound O=C(CCC1C2)C12[AlH2] IQDJKWJLZKSMGB-UHFFFAOYSA-N 0.000 description 1
- HGJBPBRHSNPZSW-UHFFFAOYSA-N O=C1OCC(C2)C12[AlH2] Chemical compound O=C1OCC(C2)C12[AlH2] HGJBPBRHSNPZSW-UHFFFAOYSA-N 0.000 description 1
- SPUSBSLWVCFSGN-UHFFFAOYSA-N OC(CC1)C(C2)C12[AlH2] Chemical compound OC(CC1)C(C2)C12[AlH2] SPUSBSLWVCFSGN-UHFFFAOYSA-N 0.000 description 1
- UTPPKDJBJUSOJG-UHFFFAOYSA-N OC(CC1)C=C1[AlH2] Chemical compound OC(CC1)C=C1[AlH2] UTPPKDJBJUSOJG-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85766706P | 2006-11-07 | 2006-11-07 | |
| US11/936,016 US8138377B2 (en) | 2006-11-07 | 2007-11-06 | Arylbicyclo[3.1.0]hexylamines and methods and compositions for their preparation and use |
| PCT/US2007/023506 WO2008057575A2 (en) | 2006-11-07 | 2007-11-07 | Novel arylbicyclo[3.1.0]hexylamines and methods and compositions for their preparation and use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010509334A JP2010509334A (ja) | 2010-03-25 |
| JP2010509334A5 true JP2010509334A5 (https=) | 2012-01-05 |
Family
ID=39365134
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009536293A Pending JP2010509334A (ja) | 2006-11-07 | 2007-11-07 | 新規アリールビシクロ［３．１．０］ヘキシルアミンならびにそれらの調製および使用のための方法および組成物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8138377B2 (https=) |
| EP (1) | EP2086328A4 (https=) |
| JP (1) | JP2010509334A (https=) |
| KR (1) | KR20090079984A (https=) |
| BR (1) | BRPI0718654A2 (https=) |
| CA (1) | CA2705457A1 (https=) |
| RU (1) | RU2009121553A (https=) |
| WO (1) | WO2008057575A2 (https=) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070043100A1 (en) | 2005-08-16 | 2007-02-22 | Hagen Eric J | Novel polymorphs of azabicyclohexane |
| EP1915146A4 (en) | 2005-07-27 | 2010-06-02 | Dov Pharmaceutical Inc | NOVEL 1-ARYL-3-AZABICYCLO [3.1.0] HEXANEES. PREPARATION AND USE FOR THE TREATMENT OF NEUROPSYCHIATRIC DISEASES |
| US20080045725A1 (en) | 2006-04-28 | 2008-02-21 | Murry Jerry A | Process For The Synthesis of (+) And (-)-1-(3,4-Dichlorophenyl)-3-Azabicyclo[3.1.0]Hexane |
| US20080269348A1 (en) * | 2006-11-07 | 2008-10-30 | Phil Skolnick | Novel Arylbicyclo[3.1.0]Hexylamines And Methods And Compositions For Their Preparation And Use |
| US9133159B2 (en) | 2007-06-06 | 2015-09-15 | Neurovance, Inc. | 1-heteroaryl-3-azabicyclo[3.1.0]hexanes, methods for their preparation and their use as medicaments |
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2007
- 2007-11-06 US US11/936,016 patent/US8138377B2/en not_active Expired - Fee Related
- 2007-11-07 CA CA2705457A patent/CA2705457A1/en not_active Abandoned
- 2007-11-07 JP JP2009536293A patent/JP2010509334A/ja active Pending
- 2007-11-07 EP EP07861821A patent/EP2086328A4/en not_active Withdrawn
- 2007-11-07 RU RU2009121553/04A patent/RU2009121553A/ru not_active Application Discontinuation
- 2007-11-07 KR KR1020097011844A patent/KR20090079984A/ko not_active Ceased
- 2007-11-07 BR BRPI0718654-1A patent/BRPI0718654A2/pt not_active IP Right Cessation
- 2007-11-07 WO PCT/US2007/023506 patent/WO2008057575A2/en not_active Ceased
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