مشارك في 482 تفاعل

408216

CC(C)(C)OC(=O)N1CC=C(c2cnc(C(=O)O)cn2)CC1
Reaction #45138
5-[1-[(2-methylpropan-2-yl)oxycarbonyl]-3,6-dihydro-2H -pyridin-4-yl]pyrazine-2-carboxylic acid
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc(C2=CCN(C(=O)OC(C)(C)C)CC2)c2oc(C#N)c(Cc3ccccc3)c2c1
Reaction #46467
4-(3-benzyl-2-cyano-5-methyl-benzofuran-7-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CC=C(c2cc3c(Br)ccnc3n2S(=O)(=O)c2ccccc2)CC1
Reaction #57201
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCC(=O)c1cc(C)c(C)cc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #58002
84
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1(C)CC(c2ccccc2C2=CCN(C(=O)OC(C)(C)C)CC2)CC(C)(C)C1
Reaction #60531
title compound
المردود 70.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(C2=CCN(C(=O)OC(C)(C)C)CC2)c(C2CC(C)(C)CC(C)(C)C2)c1
Reaction #60537
title compound
المردود 63.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)c1ncccc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #69893
3′,6′-dihydro-2′H-[3,4]bipyridinyl-2,1′-dicarboxylic acid 1′-t-butyl ester 2-methyl ester
المردود 64.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1cnccc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #69897
3,6-dihydro-2H-[4,4]bipyridinyl-1,3′-dicarboxylic acid 1-t-butyl ester 3′-methyl ester
المردود 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1ccncc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #69901
3′,6′-dihydro-2′H-[3,4′]bipyridinyl-4,1′-dicarboxylic acid 1′-t-butyl ester 4-methyl ester
المردود 85.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1occc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #69907
4-(2-methoxycarbonylfuran-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid t-butyl ester
المردود 69.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1ccoc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #69913
4-(3-methoxycarbonylfuran-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid t-butyl ester
المردود 75.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1sccc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #69919
4-(2-methoxycarbonylthiophen-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid t-butyl ester
المردود 34.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1cscc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #69923
4-(4-methoxycarbonylthiophen-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid t-butyl ester
المردود 53.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1ccsc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #69927
4-(3-methoxycarbonylthiophen-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid t-butyl ester
المردود 92.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)N1CC=C(c2ccc(NC(=O)c3ccc(S(C)(=O)=O)cc3)nc2)CC1
Reaction #70416
title compound
المردود 22.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)N1CC=C(c2ccc(COc3ccc(S(C)(=O)=O)cc3)nn2)CC1
Reaction #70419
title compound
المردود 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(C(F)(F)F)cc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #74602
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)N1CC=C(c2cccc(-n3ncc4cnc(Cl)cc43)n2)CC1
Reaction #86139
tert-butyl 4-[6-(6-chloropyrazolo[4,3-c]pyridin-1-yl)-2-pyridyl]-3,6-dihydro-2H-pyridine-1-carboxylate
المردود 92.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)N1CC=C(c2ccc(N)c([N+](=O)[O-])c2)CC1
Reaction #86418
title compound
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)N1CC=C(c2ccc(F)c(F)c2C(F)(F)F)CC1
Reaction #86696
tert-butyl 4-(3,4-difluoro-2-(trifluoromethyl)phenyl)-5,6-dihydropyridine-1(2H)-carboxylate
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
الصفحة 1التالي