6-aminohexanoic acid methyl ester hydrochloride salt

COC(=O)CCCCCNC(=O)C(F)(F)F
Reaction #47713
product ( 3 )
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)CCCCCNS(=O)(=O)c1cccc2ccccc12
Reaction #78885
6(1-naphthalenesulfonyl)aminocaproic acid methyl ester
المردود 54.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
—
Reaction #313369
oil
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COC(=O)CCCCCNS(=O)(=O)c1cccnc1
Reaction #313370
title compound
المردود 76.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COC(=O)CCCCCNC(=O)CCNC(=O)OCc1ccccc1
Reaction #336810
desired product ( 35 )
المردود 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COC(=O)CCCCCNC(=O)c1c(C)[nH]c(C=NN=C2C(=O)Nc3ccc(F)cc32)c1C
Reaction #338845
title compound
المردود 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COC(=O)CCCCCNC(=O)c1ccc(C=NN=C2C(=O)Nc3ccc(F)cc32)cc1
Reaction #338865
title compound
المردود 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COC(=O)CCCCCNC(=O)c1ccc(C=C2C(=O)Nc3ccc(F)cc32)cc1
Reaction #338873
title compound
المردود 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COC(=O)CCCCCNC(=O)c1cccc(C=C2C(=O)Nc3ccc(F)cc32)c1
Reaction #338878
title compound
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COC(=O)CCCCCNC(=O)C(COC1CCCCO1)NS(=O)(=O)c1ccc(Cl)cc1
Reaction #353455
(RS)-2-(4-chlorobenzenesulfonylamino)-N-(5-methoxycarbonylpentyl)-3-(tetrahydropyran-2-yloxy)propanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
—
Reaction #438275
oil
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)CCCCCNS(=O)(=O)c1cccnc1
Reaction #438276
title compound
المردود 76.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)CCCCCNC(C)=O
Reaction #691384
methyl 6-acetylamino-hexanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
COC(=O)CCCCCNC(=O)[C@@H](C)NC(=O)OC(C)(C)C
Reaction #707919
Boc-(D)Ala-NH(CH2)5CO2Me
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_04
COC(=O)CCCCCNC(=O)c1cccc(OC)c1O
Reaction #812307
title compound
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
COC(=O)CCCCCN1Cc2c(Br)cccc2C1=O
Reaction #1107598
title compound
المردود 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
COC(=O)CCCCCNC(=O)c1cccc(Br)c1C
Reaction #1107614
title compound
المردود 31.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
COC(=O)CCCCCNC(=O)C(F)(F)F
Reaction #1159404
product ( 3 )
المردود 86.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_06
COC(=O)CCCCCNC(=O)C(F)(F)F
Reaction #1328399
product ( 3 )
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
COC(=O)CCCCCNC(=O)/C=C/C=C/c1ccccc1[N+](=O)[O-]
Reaction #1449734
title compound
المردود 89.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
الصفحة 1التالي