Поиск подструктуры

145188

CN(C)CCNc1nc2c([N+](=O)[O-])c(O)ccc2c2c1C(=O)c1ccccc1-2
Reaction #3254
title compound
Выход 52.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(=O)C(Cc1c[nH]cn1)NC(=O)OC(C)(C)C)C(=O)OCCOc1ccc(-c2c(C#N)c(SCc3csc(-c4ccc(Cl)cc4)n3)nc(N3CCCC3)c2C#N)cc1
Reaction #174088
DOI: 10.1039/C8SC04228D
N#Cc1c(SCc2csc(-c3ccc(Cl)cc3)n2)nc(N2CC(O)C2)c(C#N)c1-c1cncs1
Reaction #178162
DOI: 10.1039/C8SC04228D
CC(C)CC(NC(=O)CCNC(=O)OC(C)(C)C)C(=O)OCCOc1ccc(-c2c(C#N)c(SCc3csc(-c4ccc(Cl)cc4)n3)nc(N3CCCC3)c2C#N)cc1
Reaction #183041
DOI: 10.1039/C8SC04228D
Cc1cc(OCCCCN2CCN(c3cccc4ccccc34)CC2)nc2c1CCC(=O)N2
Reaction #190401
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OCC#Cc1nc(-c2c(C#N)c(N)nc(SCc3csc(-c4ccc(Cl)cc4)n3)c2C#N)cs1
Reaction #198292
DOI: 10.1039/C8SC04228D
Cc1cc(OCCCCN2CCN(c3cccc4c3CCC4)CC2)nc2c1CCC(=O)N2
Reaction #221486
DOI: 10.1039/C8SC04228D
CC(NC(=O)C(CCCCNC(=O)OC(C)(C)C)NC(=O)OC(C)(C)C)C(=O)OCCOc1ccc(-c2c(C#N)c(SCc3csc(-c4ccc(Cl)cc4)n3)nc(N3CCCC3)c2C#N)cc1
Reaction #241544
DOI: 10.1039/C8SC04228D
N#Cc1c(N)nc(SCc2coc(-c3ccc(Cl)cc3)n2)c(C#N)c1-c1ccc(OCC(O)CO)cc1
Reaction #244629
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2c(C#N)c(NCCCn3ccnc3)nc3sc(C(N)=O)c(N)c23)o1
Reaction #307312
3-Amino-5-cyano-6-(3-imidazol-1-ylpropylamino)-4-(5-methylfuran-2-yl)thieno[2,3-b]-pyridine-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC[C@@H](COc2ccc(-c3c(C#N)c(N)nc(SCc4coc(-c5ccc(Cl)cc5)n4)c3C#N)cn2)O1
Reaction #329346
2′-Amino-6′-({[2-(4-chlorophenyl)-1,3-oxazol-4-yl]methyl}thio)-6-{[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]methoxy}-3,4′-bipyridine-3′,5′-dicarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(N)nc(SCc2coc(-c3ccc(Cl)cc3)n2)c(C#N)c1-c1ccc(OC[C@@H](O)CO)nc1
Reaction #329356
2′-Amino-6′-({[2-(4-chlorophenyl)-1,3-oxazol-4-yl]methyl}thio)-6-{[(2S)-2,3-dihydroxypropyl]-oxy}-3,4′-bipyridine-3′,5′-dicarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)=CNc1nccc2c1CCCC2
Reaction #378116
DOI: 10.1039/C8SC04228D
CC(NC(=O)C1CCCN1C(=O)OC(C)(C)C)C(=O)OCCOc1ccc(-c2c(C#N)c(SCc3csc(-c4ccc(Cl)cc4)n3)nc(N3CCCC3)c2C#N)cc1
Reaction #384778
DOI: 10.1039/C8SC04228D
—
Reaction #442792
polyurethane
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN)ccnc1NC(=O)OC(C)(C)C
Reaction #448561
title compound
Выход 84.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCNc1nc2c([N+](=O)[O-])c(O)ccc2c2c1C(=O)c1ccccc1-2
Reaction #464778
title compound
Выход 52.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC[C@H](COc2ccc(-c3c(C#N)c(N)nc(SCc4coc(-c5ccc(Cl)cc5)n4)c3C#N)cc2)O1
Reaction #490197
2-Amino-6-({[2-(4-chlorophenyl)-1,3-oxazol-4-yl]methyl}sulfanyl)-4-(4-{[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methoxy}phenyl)pyridine-3,5-dicarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(N)nc(SCc2coc(-c3ccc(Cl)cc3)n2)c(C#N)c1-c1ccc(OC[C@H](O)CO)cc1
Reaction #490198
2-Amino-6-({[2-(4-chlorophenyl)-1,3-oxazol-4-yl]methyl}sulfanyl)-4-(4-{[(2R)-2,3-dihydroxypropyl]oxy}phenyl)pyridine-3,5-dicarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(N)nc(SCc2coc(-c3ccc(Cl)cc3)n2)c(C#N)c1-c1ccc(OC[C@@H](O)CO)cc1
Reaction #490199
product
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее