Substructure Search

1197706

N#CC1CCCCC1N
Reaction #90935
diastereomeric mixture
Yield 78.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCCC[C@H]1CN
Reaction #162093
14d
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCCCC1C#N
Reaction #251194
DOI: 10.1039/C8SC04228D
O=C(O)C1CCCCC1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O
Reaction #271737
DOI: 10.1039/C8SC04228D
N#CC1CCCCC1N(Cc1ccccc1)Cc1ccccc1
Reaction #319470
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCCCC1C#N
Reaction #319486
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1CCCCC1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O
Reaction #364137
3-[2-(2-cyanocyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine
Yield 30.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCCCC1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O
Reaction #364138
3-[2-(2-carboxycyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCCC[C@H]1CN
Reaction #614117
14d
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1c(F)cc(C(=O)NC2CCCCC2C#N)cc1F
Reaction #689186
N-(2-cyanocyclohexyl)-3,5-difluoro-4-(2-propynyloxy)benzamide
Yield 75.6%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1c(F)cc(C(=O)NC2CCCCC2C#N)cc1F
Reaction #778238
DOI: 10.1039/C8SC04228D
C[C@H]1C[C@@H](c2ccncc2N)C[C@@H](NC(=O)OC(C)(C)C)[C@H]1C#N
Reaction #792482
(+/−)-tert-butyl (1R,2S,3S,5R)-5-(3-aminopyridin-4-yl)-2-cyano-3-methylcyclohexylcarbamate
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@H](c2ccncc2NC(=O)c2ccc(F)c(-c3c(F)cccc3F)n2)C[C@H](NC(=O)OC(C)(C)C)[C@@H]1C#N
Reaction #792483
tert-butyl (1S,2R,3R,5S)-2-cyano-5-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-3-methylcyclohexylcarbamate
Yield 27.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1CCCCC1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O
Reaction #893538
DOI: 10.1039/C8SC04228D
C[C@H]1C[C@@H](c2ccncc2N)C[C@@H](NC(=O)OC(C)(C)C)[C@H]1C#N
Reaction #966397
(+/−)-tert-butyl (1R,2S,3S,5R)-5-(3-aminopyridin-4-yl)-2-cyano-3-methylcyclohexylcarbamate
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@H](c2ccncc2NC(=O)c2ccc(F)c(-c3c(F)cccc3F)n2)C[C@H](NC(=O)OC(C)(C)C)[C@@H]1C#N
Reaction #966398
tert-butyl (1S,2R,3R,5S)-2-cyano-5-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-3-methylcyclohexylcarbamate
Yield 27.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1CCCCC1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O
Reaction #1052548
3-[2-(2-cyanocyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine
Yield 30.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCCCC1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O
Reaction #1052549
3-[2-(2-carboxycyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1CCCCC1n1c(=O)[nH]c2cnc3[nH]ccc3c21
Reaction #1302842
DOI: 10.1039/C8SC04228D
N#CC1CCCCC1N(Cc1ccccc1)Cc1ccccc1
Reaction #1307740
DOI: 10.1039/C8SC04228D
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