(1S,2S)—N,N′-dimethyl-cyclohexane-1,2-diamine

COC(=O)c1cc(-c2ccc(C)cn2)c2cnn(-c3ccccc3)c2c1
Reaction #88089
4-(5-Methyl-pyridin-2-yl)-1-phenyl-1H-indazole-6-carboxylic acid methyl ester
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)c1cc(N)n(-c2ccc(F)c(O)c2)n1
Reaction #88905
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)[Si](Oc1ccc(-n2nc(C(C)(C)C)cc2N)cc1CO)(C(C)C)C(C)C
Reaction #88932
title compound
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(-n2cccn2)c(C(=O)N2CCC[C@H](C)[C@@H]2CNc2ccc(C(F)(F)F)cn2)c1
Reaction #89156
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(-n2nccn2)c(C(=O)O)c1
Reaction #89187
title compound
Ausbeute 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(-n2cccn2)c(C#N)n1
Reaction #89366
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(F)c(C(=O)O)c1-n1nccn1
Reaction #89552
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc2c(c1)C(C)(C)c1[nH]c3c(N)c(C#N)ccc3c1C2=O
Reaction #90133
title compound
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccc2cnn(-c3ccccc3)c2c1
Reaction #533414
1-phenyl-1H-indazole-6-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C1CCCN1c1ccc(-c2cnc3ncc(C4(c5ccc6ncccc6c5)CC4)n3c2)cc1F
Reaction #587378
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
Cc1ccn(-c2ccc(C3(C(=O)N4CCC5(C4)OC(=O)c4cnccc45)CC3)cc2)n1
Reaction #591484
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C1O[C@]2(CCN(C(=O)C3(c4ccc(-n5cc6ccccc6n5)cc4)CC3)C2)c2ccncc21
Reaction #591485
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C1O[C@]2(CCN(C(=O)C3(c4ccc(-n5cnc6ccccc65)cc4)CC3)C2)c2ccncc21
Reaction #591486
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C1O[C@]2(CCN(C(=O)C3(c4ccc(-n5ncc6ccccc65)cc4)CCC3)C2)c2ccncc21
Reaction #591496
(1R)-1′-({1-[4-(1H-Indazol-1-yl)phenyl]cyclobutyl}carbonyl)-3H-spiro[furo[3,4-c]pyridine-1,3′-pyrrolidin]-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C1O[C@]2(CCN(C(=O)C3(c4ccc(-n5ccccc5=O)cc4)CC3)C2)c2ccccc21
Reaction #591527
(1R)-1′-({1-[4-(2-Oxopyridin-1(2H)-yl)phenyl]cyclopropyl}carbonyl)-3H-spiro[2-benzofuran-1,3′-pyrrolidin]-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
N#CC1(c2ccc(-n3ccc(C(F)(F)F)n3)cc2)CC1
Reaction #591534
1-{4-[3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}cyclopropanecarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC(C)(C)OC(=O)NCc1cccc(-n2cccn2)c1
Reaction #600479
tert-butyl-3-(1H-pyrazol-1-yl)benzylcarbamate
Ausbeute 70.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
Cc1ccn(-c2ccc(C3(C(=O)N4CCC5(C4)OC(=O)c4cnccc45)CC3)cc2)n1
Reaction #645022
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O=C1O[C@]2(CCN(C(=O)C3(c4ccc(-n5cc6ccccc6n5)cc4)CC3)C2)c2ccncc21
Reaction #645023
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O=C1O[C@]2(CCN(C(=O)C3(c4ccc(-n5cnc6ccccc65)cc4)CC3)C2)c2ccncc21
Reaction #645024
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
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