Recherche de Sous-structure

775375

CCOC(=O)c1cnn(C2CCCC2)c1N
Reaction #41164
5-amino-1-cyclopentyl-1H-pyrazole-4-carboxylic acid ethyl ester
Rendement 79.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnn(C2CCCC2)c1C(F)(F)F
Reaction #41169
1-cyclopentyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid ethyl ester
Rendement 52.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Br)ccc1-c1ccnn1C1CCCC1
Reaction #156282
5-(4-bromo-2-nitrophenyl)-1-cyclopentyl-1H-pyrazole
Rendement 72.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc(Br)cc2[N+](=O)[O-])n(C2CCCC2)n1
Reaction #156291
5-(4-bromo-2-nitrophenyl)-1-cyclopentyl-3-methyl-1H-pyrazole
Rendement 62.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2CC3CCC2C3)N1Cc1cccc(Cl)c1Cl
Reaction #252239
DOI: 10.1039/C8SC04228D
CC1(C)C(=O)N(C2CC3CCC2C3)N1Cc1ccccc1Cl
Reaction #259478
DOI: 10.1039/C8SC04228D
CC1(C)C(=O)N(C2CC3CCC2C3)N1Cc1cc(Cl)ccc1Cl
Reaction #275943
DOI: 10.1039/C8SC04228D
CC1(C)C(=O)N(C2CC3CCC2C3)N1Cc1ccc(F)cc1Cl
Reaction #276547
DOI: 10.1039/C8SC04228D
Cc1cc(N)n(C2CCCC2)n1
Reaction #563211
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(C2CCCC2C)c(N)c1C#N
Reaction #574424
1-(2-methylcyclopentyl)-3-methyl-5-amino-1H-pyrazole-4-carbonitrile
Rendement 56.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(C2CCCC2)c(N)c1C#N
Reaction #574428
1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carbonitrile
Rendement 70.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(Cc2ccccc2)nn(C2CCCC2)c1N
Reaction #574446
1-cyclopentyl-3-phenylmethyl-5-amino-1H-pyrazole-4-carbonitrile
Rendement 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(C2CCCC2)c2c1CCN(c1ccc(OC)cc1)C2=O
Reaction #699586
1-cyclopentyl-3-ethyl-6(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1-H-pyrazolo[3,4-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)N1C(=O)C(C2=NS(=O)(=O)c3cc(NS(C)(=O)=O)ccc3N2)=C(O)[C@@H]2CCC[C@@H]21.Cl
Reaction #818523
cis-N-[3-(1-dimethylamino-4-hydroxy-2-oxo-2,4a,5,6,7,7a-hexahydro-1H-[1]pyrindin-3-yl)-1,1-dioxo-1,4-dihydro-1λ6-benzo[1,2,4]thiadiazin-7-yl]-methanesulfonamide hydrochloride
Rendement 52.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2CC3CCC2C3)N1Cc1ccccc1Cl
Reaction #976016
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2CC3CCC2C3)N1Cc1cccc(Cl)c1Cl
Reaction #976017
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2CC3CCC2C3)N1Cc1cc(Cl)ccc1Cl
Reaction #976018
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2CC3CCC2C3)N1Cc1ccc(F)cc1Cl
Reaction #976019
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2CC3CCC2C3)N1Cc1cc(F)ccc1Cl
Reaction #976020
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2CC3CCC2C3)N1c1cccc(Cl)c1Cl
Reaction #976068
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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