部分構造検索

CNC1CCCCC1NC

Cc1ccc2c(N3CCN(CCc4cccc(N5C(=O)NC6CCCCC65)c4)CC3)cccc2n1
Reaction #44168
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1CCCC[C@H]1NC(=O)c1ccc([N+](=O)[O-])c(O)c1
Reaction #54531
titled product
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1CCCC[C@H]1NC(=O)c1ccc(C#N)cc1
Reaction #54532
amide
収率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1CCCC[C@H]1NC(=O)c1cccc(Cl)c1
Reaction #54533
amide
収率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CCN([C@H]2CCCC[C@H]2NC(=O)c2cc(C)cc(C)c2)C1
Reaction #54539
cis-N-[2-(3-acetyloxy-1-pyrrolidinyl)cyclohexyl]-3,5-dimethylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1C[C@@H]2C[C@@H]2[C@H]1N1C(=O)c2ccccc2C1=O)OCc1ccccc1
Reaction #84685
title compound
収率 65.6%DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1C[C@@H]2C[C@@H]2[C@H]1N1C(=O)c2ccccc2C1=O
Reaction #84686
crude compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(NC(=O)OCC[Si](C)(C)C)C(N)C1
Reaction #84708
title compound
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(Nc2cc(N[C@@H]3CCCC[C@@H]3NC(=O)OC(C)(C)C)ccc2C#N)c1
Reaction #171974
tert-butyl (1S,2R)-2-(4-cyano-3-(m-tolylamino)phenylamino)cyclohexylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCCC[C@H]1Nc1cc(Br)c(C#N)cc1F
Reaction #172017
tert-butyl (1S,2R)-2-(5-bromo-4-cyano-2-fluorophenylamino)cyclohexylcarbamate
収率 93.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc(N[C@@H]3CCCC[C@@H]3N)c(F)cc2C(N)=O)sn1
Reaction #172018
titled compound
収率 74.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCCC[C@H]1Nc1cc(Nc2cc(-c3ccccc3)no2)c(C#N)cc1F
Reaction #172041
tert-butyl (1S,2R)-2-(4-cyano-2-fluoro-5-(3-phenylisoxazol-5-ylamino)phenylamino)cyclohexylcarbamate
収率 20.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CC(NC(C)(C)C)CCC1N1CCC(NC(=O)OCc2ccccc2)C1=O
Reaction #175812
DOI: 10.1039/C8SC04228D
Clc1ccc(CCNC2CCCCC2N2CCCC2)cc1Cl
Reaction #177955
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CC(C(=O)O)CCC1NC(=O)OCc1ccccc1
Reaction #178459
DOI: 10.1039/C8SC04228D
O=C(C1CCCC1)N1CCC(N2CCC(N3C(=O)NC4CCCCC43)CC2)CC1
Reaction #182613
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCC12CCCCC1(Cc1ccc(C#N)cc1)NC(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #184383
DOI: 10.1039/C8SC04228D
O=C1CCCN1CCC(=O)N1CCC(N2CCC(N3C(=O)NC4CCCCC43)CC2)CC1
Reaction #186993
DOI: 10.1039/C8SC04228D
COC1(OC)CCCC(N2CCCC2)C1N(C)C(=O)Cc1ccc(Cl)c(Cl)c1
Reaction #196436
DOI: 10.1039/C8SC04228D
COC(=O)N1CCN(C(=O)Cc2ccc(Cl)c(Cl)c2)C2C(N3CCCC3)CCCC21
Reaction #200049
DOI: 10.1039/C8SC04228D
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