بحث البنية الفرعية

4672

CN(CCO)C(=O)c1ccco1
Reaction #3167
N-(2-hydroxyethyl)-N-methylfuranamide
المردود 57.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(-c2ccccc2)nc(-c2cccc([N+](=O)[O-])c2)c1CN1CCN(C(=O)c2ccco2)CC1
Reaction #4785
6-methyl-5-[4-(2-furoyl)piperazin-1-ylmethyl]-4-(3-nitrophenyl)-2-phenylpyrimidine
المردود 97.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCSc1ccncc1)c1ccco1
Reaction #6216
desired compound
المردود 87.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(CNC(=O)c4ccco4)c3C2=O)C(=O)N1
Reaction #10063
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}-2-furylcarboxamide
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccco4)c3C2=O)C(=O)N1
Reaction #10079
product
المردود 88.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Cc2ccc(F)cc2)o1
Reaction #11334
5-(4-fluorobenzyl)-2-furan carboxylic acid chloride
المردود 100.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)c1ccco1)[C@H](Oc1ccc2c(cnn2-c2ccncc2)c1)c1ccccc1
Reaction #41415
title compound
المردود 65.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2ncc3cc(O[C@H](c4ccccc4)[C@H](C)NC(=O)c4ccco4)ccc32)cc1
Reaction #41419
title compound
المردود 48.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(Nc1ccc2sc(C(=O)N[C@H]3CN4CCC3CC4)cc2c1)c1ccco1
Reaction #43756
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(F)c2oc(-c3ccco3)nc2c1C#N
Reaction #45638
compound
المردود 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N(NC(=O)c1ccccc1)C(=O)c1ccco1
Reaction #49933
N'-t-butyl-N-benzoyl-N'-(2-furoyl)hydrazine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2c(N3CCN(C(=O)c4ccco4)CC3)n(-c3ccccc3)c3ccccc23)CC1
Reaction #54487
2-[4-(2-furoyl)-1-piperazinyl]-1-phenyl-indole 3-carboxylic acid 4-methyl-piperazide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Br)cc1)c1cc2ccccc2o1
Reaction #57560
N-(4-bromophenyl)-1-benzofuran-2-carboxamide
المردود 82.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](C(C)C)N(C)S(=O)(=O)c1ccc(-c2ccc(NC(=O)c3cc4ccccc4o3)cc2)cc1
Reaction #57594
methyl N-({4′-[(1-benzofuran-2-ylcarbonyl)amino]-1,1′-biphenyl-4-yl}sulfonyl)-N-methyl-D-valinate
المردود 86.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(=O)c2ccc(C#N)o2)c(N2CCCCC2)c1
Reaction #61167
title compound
المردود 60.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)Nc2ccc(-n3ccnc3)cc2N2CCCCC2)o1
Reaction #61170
title compound
المردود 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc(NC(=O)c2ccc(C#N)o2)c(N2CCCCC2)c1
Reaction #61174
title compound
المردود 63.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)Nc2ccccc2N2CCC(F)(F)CC2)o1
Reaction #61176
title compound
المردود 36.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(NC(=O)c2ccc(C#N)o2)c(N2CCCCC2)c1
Reaction #61179
title compound
المردود 54.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)Nc2cccc(Cl)c2N2CCCCC2)o1
Reaction #61182
title compound
المردود 10.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي