بحث البنية الفرعية

1292619

CN1CCc2cc(Nc3cc(Br)cn(C)c3=O)ccc2C1
Reaction #190643
DOI: 10.1039/C8SC04228D
CCOC(=O)C(OCC)n1cccc(Nc2ccccc2)c1=O
Reaction #230991
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC[C@H]1C(=O)Nc1ccccc1
Reaction #313421
BOC-proline anilide
المردود 129.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c(Nc2ccccc2)cc(-c2ccccn2)cn1-c1ccccc1
Reaction #316863
subject compound
المردود 85.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(NC(=O)c2ccc(C(C)(C)C)cc2)cccc1-c1cc(Nc2ccc(C(=O)N3CCC(O)CC3)cc2)c(=O)n(C)c1
Reaction #371333
DOI: 10.1039/C8SC04228D
CCOC(C(=O)NCc1ccc2c(N)noc2c1)n1cccc(Nc2ccccc2)c1=O
Reaction #388695
DOI: 10.1039/C8SC04228D
N#Cc1ccccc1-c1ccc(CNc2c(NCc3ccccc3)cc[nH]c2=O)cc1
Reaction #569672
4-benzylamino-3-(2'-cyanobiphenyl-4-ylmethylamino)-1,2-dihydro-2-oxopyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c(Nc2ccccc2)cc(-c2ccccn2)cn1-c1ccccc1
Reaction #585026
subject compound
المردود 85.5%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2ccc(Br)cc2c(O)c1Nc1ccccc1
Reaction #608030
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c(Nc2ccccc2)cc(-c2ccccn2)cn1-c1ccccc1
Reaction #634894
subject compound
المردود 85.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(Nc2cc(-c3cccc(NC(=O)c4ccc(C(C)(C)C)cc4)c3C)cn(C)c2=O)cc1
Reaction #639030
4-{5-[3-(4-tert-butyl-benzoylamino)-2-methylphenyl]-1-methyl-2-oxo-1,2-dihydropyridin-3-ylamino}-benzoic acid ethyl ester
المردود 77.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(NC(=O)c2ccc(C(C)(C)C)cc2)cccc1-c1cc(Nc2ccc(C(=O)O)cc2)c(=O)n(C)c1
Reaction #639031
4-{5-[3-(4-tert-butyl-benzoylamino)-2-methyl-phenyl]-1-methyl-2-oxo-1,2-dihydropyridin-3-ylamino}-benzoic acid
المردود 56.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(NC(=O)c2ccc(C(C)(C)C)cc2)cccc1-c1cc(Nc2ccc(C(=O)N3CCC(O)CC3)cc2)c(=O)n(C)c1
Reaction #639032
4-tert-butyl-N-(3-{5-[4-(4-hydroxy-piperidine-1-carbonyl)-phenylamino]-1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl}-2-methyl-phenyl)-benzamide
المردود 61.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCc1c(-c2cc(Nc3ccc(C4CN(C)C4)cc3)c(=O)n(C)c2)ccnc1N1CCn2c(cc3c2CCCC3)C1=O
Reaction #680147
239d
المردود 54.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cc([N+](=O)[O-])cn(C)c2=O)c(C)c1
Reaction #685238
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)c1cc(Nc2ccc(C)cc2C)c(=O)n(C)c1
Reaction #685239
product
المردود 3.7%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2ccc(Br)cc2c(O)c1Nc1ccccc1
Reaction #711155
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(c1ccccc1)c1c(O)c2cc(Br)ccc2[nH]c1=O
Reaction #711156
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(c1ccccc1)c1c(O)c2cc(Br)ccc2[nH]c1=O
Reaction #711157
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(c1ccccc1)c1c(O)c2cc(Br)ccc2[nH]c1=O
Reaction #711158
title compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي