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c1nc[nH]n1

COc1ccc(-c2nnc(CC(=O)O)n2-c2ccccc2)cc1
Reaction #4695
5-(4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole-3-acetic acid
Выход 98.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N(Cc2ccc(Cl)c(O)c2)n2cnnc2)cc1
Reaction #48203
4-[(4-Chloro-3-hydroxy-benzyl)-[1,2,4]triazol-4-yl-amino]-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N(Cc2ccc(Cl)c(OS(N)(=O)=O)c2)n2cnnc2)cc1
Reaction #48204
Sulfamic Acid 2-chloro-5-{[(4-cyano-phenyl)-[1,2,4]triazol-4-yl-amino]-methyl}-phenyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncn(-c2cc(F)ccc2CNC(=O)c2nc3n(c(=O)c2O)CCOC3(CO)CCl)n1
Reaction #56658
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(SCCCC=O)nnc1-c1ccc2ncccc2c1
Reaction #61508
title compound
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)c1ccc2c(c1)CCN(CCCCSc1nnc(-c3ccc4ncccc4c3)n1C)CC2
Reaction #61509
title compound
Выход 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)[nH]1
Reaction #64528
title compound
Выход 19.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1
Reaction #64529
title compound
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cccc([N+](=O)[O-])c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1
Reaction #64538
title compound
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1
Reaction #64555
title compound
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(Br)cc1F
Reaction #64566
title compound
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(Br)cc1F
Reaction #64571
title compound
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1F
Reaction #64577
title compound
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(-c2c(F)cccc2Cl)nn1-c1ccc(Br)cc1
Reaction #87504
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)C#Cc1ccc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)cc1
Reaction #87507
desired product
Выход 107.3%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc(Cl)c1-c1nc(Cl)n(-c2ccc(Br)cc2)n1
Reaction #87508
desired product
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)cc1
Reaction #87534
desired product
DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccc(Cl)c(-c2nn(-c3ccc(Cl)c(F)c3)c(=O)[nH]2)c1
Reaction #87643
5-(5-(Aminomethyl)-2-chlorophenyl)-2-(4-chloro-3-fluorophenyl)-2H-1,2,4-triazol-3(4H)-one
Выход 95.4%DOI: 10.6084/m9.figshare.5104873.v1
NCc1cc(-c2nn(-c3ccc(Cl)cc3)c(=O)[nH]2)c(Cl)cc1F
Reaction #87646
desired product
Выход 55.6%DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccc(Cl)c(-c2nn(-c3ccc(F)c(Cl)c3)c(=O)[nH]2)c1
Reaction #87673
desired product
Выход 63.6%DOI: 10.6084/m9.figshare.5104873.v1
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