Substructure Search

N#Cc1ccc(N)cc1

Cc1c(C#N)c(N)c([N+](=O)[O-])c(N2CC[C@H](N(C)C)C2)c1-c1ccccc1
Reaction #45831
compound
Yield 90.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(N)c(N)c(N2CC[C@H](N(C)C)C2)c1-c1ccccc1
Reaction #45832
compound
Yield 97.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(N)c(NC(=O)C(C)(C)C)c(N2CC[C@H](N(C)C)C2)c1-c1ccccc1
Reaction #45833
compound
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2[nH]c(C(C)(C)C)nc2c1C#N
Reaction #45834
2-tert-Butyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-6-phenyl-1H-benzimidazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2ccc(C#N)cc2)CC1
Reaction #48143
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCOCC2)n3-c2ccc(C#N)cc2)CC1
Reaction #48149
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSC(N)=Nc1ccc(C#N)cc1
Reaction #53321
methyl N′-(4-cyanophenyl)-carbamimidothioate
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(c2ccc(C#N)c(C(F)(F)F)c2)C(=O)N1CCCCOCc1ccccc1
Reaction #64225
expected product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N)c(I)c1
Reaction #86912
title compound
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[Si](CC)(CC)c1[nH]c2ccc(C#N)cc2c1CCO
Reaction #86913
title compound
Yield 51.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NN(C(=O)NC(=O)c1c(F)cccc1Cl)c1ccc(C#N)cc1
Reaction #87533
tert-butyl 2-((2-chloro-6-fluorobenzoyl)carbamoyl)-2-(4-cyanophenyl)hydrazinecarboxylate
Yield 92414.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #87778
pure product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)c(N)c(I)c1
Reaction #88214
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCCN(C(=O)c2cc(C#N)ccc2-n2nccn2)[C@@H]1CNc1ncc(C(F)(F)F)cn1
Reaction #89532
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N[C@H](Cc2ccccc2)C(N)=O)cc1Br
Reaction #171998
(R)-2-(3-bromo-4-cyanophenylamino)-3-phenylpropanamide
Yield 23.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #171999
crude residue
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N[C@H](CC2CCCCC2)C(N)=O)cc1Br
Reaction #172006
(R)-2-(3-bromo-4-cyanophenylamino)-3-cyclohexylpropanamide
Yield 63.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc(N[C@H](CC3CCCCC3)C(N)=O)ccc2C#N)sn1
Reaction #172007
(R)-2-(4-cyano-3-(3-methylisothiazol-5-ylamino)phenylamino)-3-cyclohexylpropanamide
Yield 99.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CN)cc(I)c1N
Reaction #173316
DOI: 10.1039/C8SC04228D
CC1C(C(C)(C)OC(N)=O)CCN1c1ccc(C#N)c2ccccc12
Reaction #173603
DOI: 10.1039/C8SC04228D
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