Substructure Search

15896

CC(C)(C)OC(=O)NC(=N)c1ccc(CNC(=O)[C@@H]2CCc3ncc(NC4CCCC4)c(=O)n32)cc1
Reaction #11057
intermediate 6a
Yield 57.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC2CCCC2)c(I)c1
Reaction #11512
Methyl 4-(N-cyclopentylamino)-3-iodobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NNC1CCCC1
Reaction #41163
N′-cyclopentyl-hydrazinecarboxylic acid tert-butyl ester
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(OCc2ccccc2)ccn1-c1ccc(O[C@H]2CCN(C3CCCC3)C2)cc1
Reaction #43314
title compound
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(C2CCC(=O)C2)c2oc(C3CC3)nc2c1C#N
Reaction #45869
compound
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c([C@@H]2CC[C@@H](N(C)C)C2)c2oc(C3CC3)nc2c1C#N
Reaction #45870
2-cyclopropyl-7-[(1R*,3R*)-3-(dimethylamino)cyclopentyl]-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile
Yield 41.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1(C#N)CCCC1
Reaction #49061
title product
Yield 90.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1(C#N)CCCC1
Reaction #49062
title product
Yield 96.5%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(N2CCCC2)CCCC1
Reaction #49068
title compound
Yield 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C1(C#N)CCCC1
Reaction #49070
title compound
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(N2CCC2)CCCC1
Reaction #49072
title compound
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccccc1)C1(C#N)CCCC1
Reaction #49086
title compound
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #49089
solid
Yield 49.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCN(C)C1(C#N)CCCC1
Reaction #49092
title compound
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(N2CC=CC2)CCCC1
Reaction #49094
title compound
Yield 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN1C1(C#N)CCCC1
Reaction #49096
title compound
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncc(N[C@@H]3C[C@H]4CC[C@@H]3C4)nc2cc1OC
Reaction #51627
titled product
DOI: 10.6084/m9.figshare.5104873.v1
c1cnc(NC2CCN(C3CCCC3)CC2)nc1
Reaction #55029
N-(1-cyclopentyl-4-piperidinyl)-2-pyrimidinamine
DOI: 10.6084/m9.figshare.5104873.v1
c1cnc(NC2CCN(C3CCCC3)CC2)nc1
Reaction #56422
N-(1-cyclopentyl-4-piperidinyl)-2-pyrimidinamine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNN=C1CCCC1
Reaction #57463
tert-butyl N-[(1S,2R)-1-benzyl-3-(2-cyclopentylidenhydrazino)-2-hydroxypropyl]carbamate
Yield 14.0%DOI: 10.6084/m9.figshare.5104873.v1
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