1-aminocyclohexanecarboxylic acid

O=C(NC1(C(=O)O)CCCCC1)c1ccco1
Reaction #161000
title compound
المردود 237.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC1(C(=O)O)CCCCC1)c1ccc(=O)oc1
Reaction #161015
title compound
المردود 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC1(C(=O)O)CCCCC1)c1ccc(F)cc1
Reaction #161016
title compound
المردود 660.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1oncc1C1=NC2(CCCCC2)C(=O)O1
Reaction #161022
title compound
المردود 16.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1OC(C2CCCC2)=NC12CCCCC2
Reaction #161023
title compound
المردود 42.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)c1nccs1)OC)N(C)C(=O)[C@@H](NC(=O)C1(N)CCCCC1)C(C)C
Reaction #161926
#52
المردود 35.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC1(C(=O)O)CCCCC1)c1ccco1
Reaction #193915
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC1(C(=O)O)CCCCC1C(=O)OCC1c2ccccc2-c2ccccc21
Reaction #276975
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(NC1(C(=O)O)CCCCC1)c1ccc(F)cc1
Reaction #298214
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN(C)CCCOc1cc(-c2nc(C(=O)NC3(C(=O)O)CCCCC3)ccc2-c2ncc(Cl)cc2Cl)ccc1Cl.Cl
Reaction #331245
1-{[(3,5-dichloro-2′-{4-chloro-3-[3-(dimethylamino)propoxy]phenyl}-2,3′-bipyridin-6′-yl)carbonyl]amino}cyclohexanecarboxylic acid hydrochloride
المردود 100.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC(=O)C1(N)CCCCC1.Cl
Reaction #331250
Methyl 1-aminocyclohexanecarboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC1(N)CCCCC1=C=O
Reaction #340244
1-amino-1-methoxy-carbonylcyclohexane
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=C(NC1(C(=O)O)CCCCC1)OCc1ccccc1
Reaction #363431
1-(benzyloxycarbonylamino)cyclohexane-1-carboxylic acid
المردود 89.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
COC(=O)C1(N)CCCCC1
Reaction #372549
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1OC(C2CCCC2)=NC12CCCCC2
Reaction #407197
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)OC(=O)NC1(C(=O)O)CCCCC1
Reaction #439383
desired product
المردود 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
NC1(CO)CCCCC1
Reaction #485999
oil
المردود 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
O=C(NC1(C(=O)O)CCCCC1)c1ccco1
Reaction #535905
title compound
المردود 237.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C(NC1(C(=O)O)CCCCC1)c1ccc(=O)oc1
Reaction #535921
title compound
المردود 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C(NC1(C(=O)O)CCCCC1)c1ccc(F)cc1
Reaction #535922
title compound
المردود 660.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
الصفحة 1التالي