gabapentin

COC(=O)C[C@H](NC(=O)OC(C)(C)C)C(=O)O.NCC1(CC(=O)O)CCCCC1
Reaction #57043
Boc-Asp(OMe) Gabapentin
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)O.NCC1(CC(=O)O)CCCCC1
Reaction #57044
Boc-Tyr Gabapentin
Yield 106.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cl.NCC1(CC(=O)OCc2ccccc2)CCCCC1
Reaction #58790
product ( 6 )
Yield 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=CCOC(=O)CC1(CN)CCCCC1.Cl
Reaction #58793
product ( 13 )
Yield 88.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(O)CC1(CNC(=O)OC2CCCCC2=O)CCCCC1
Reaction #339483
compound 46
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(=O)O[C@@H]1CCC[C@H]1OC(=O)NCC1(CC(=O)O)CCCCC1
Reaction #339485
compound 48
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CCOC(=O)CC1(CN)CCCCC1
Reaction #458906
Ethyl 1-aminomethyl-1-cyclohexane-acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
CC(C)C(Cl)OC(=O)NCC1(CC(=O)O)CCCCC1
Reaction #471724
title compound
Yield 77.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C1CC[NH2+]CC1.CC(=O)C=C(C)NCC1(CC(=O)[O-])CCCCC1
Reaction #471737
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C1CC[NH2+]CC1.O=C([O-])CC1(CNCC=C2CCOC2=O)CCCCC1
Reaction #471738
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C1CC[NH2+]CC1.COC(=O)C1=C(NCC2(CC(=O)[O-])CCCCC2)CCC1
Reaction #471739
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C1CC[NH2+]CC1.CCOC(=O)C(C(=O)OCC)=C(C)NCC1(CC(=O)[O-])CCCCC1
Reaction #471740
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCCC[N+](CCCC)(CCCC)CCCC.NCC1(CC(=O)[O-])CCCCC1
Reaction #476540
title compound ( 11 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(OC(=O)NCC1(CC(=O)O)CCCCC1)OC(=O)C(C)C
Reaction #476541
title compound ( 12 )
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(C)C(Cl)OC(=O)NCC1(CC(=O)O)CCCCC1
Reaction #544463
title compound
Yield 77.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
C1CC[NH2+]CC1.CC(=O)C=C(C)NCC1(CC(=O)[O-])CCCCC1
Reaction #544476
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
C1CC[NH2+]CC1.O=C([O-])CC1(CNCC=C2CCOC2=O)CCCCC1
Reaction #544477
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
C1CC[NH2+]CC1.COC(=O)C1=C(NCC2(CC(=O)[O-])CCCCC2)CCC1
Reaction #544478
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
C1CC[NH2+]CC1.CCOC(=O)C(C(=O)OCC)=C(C)NCC1(CC(=O)[O-])CCCCC1
Reaction #544479
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
CCCC(Cl)OC(=O)NCC1(CC(=O)O)CCCCC1
Reaction #544481
crude product ( 133 )
Yield 62.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
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