部分構造検索

CC(C)C#N

CN1CCC(C#N)(NC(=O)C(CC2CCCCC2)NC2=NS(=O)(=O)c3ccccc32)CC1
Reaction #53524
desired product
収率 49.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCC(C#N)(NC(=O)C(CC2CCCCC2)NC2=NS(=O)(=O)c3ccccc32)CC1
Reaction #53525
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCC(C#N)(NC(=O)C(CC(C)(C)C)NC2=NS(=O)(=O)c3ccccc32)CC1
Reaction #53526
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)N1CCC(C#N)(NC(=O)C(CC2CCCCC2)NC2=NS(=O)(=O)c3ccccc32)C1
Reaction #53527
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(NC(=O)C(CC2CCCCC2)NC2=NS(=O)(=O)c3ccccc32)CCN(C2CCCCC2)C1
Reaction #53528
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OCC(C#N)(c1ccc(Cl)cc1)c1ccccc1Cl
Reaction #56542
2-cyano-2-(2-chlorophenyl)-2-(4-chlorophenyl)ethyl methane sulfonate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CC(C#N)C(OC)OC)c2c(c1OC)OCC=C2
Reaction #62746
yellow oil
収率 62.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C#N)c1csc(-c2ccnc3[nH]ncc23)n1
Reaction #72949
desired product
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CN(C(=O)OCc1ccccc1)C2
Reaction #157973
2-benzyl 7-tert-butyl 2,7-diazaspiro[3.5]nonane-2,7-dicarboxylate
収率 85.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC(C#N)CC1c1ncc(-c2ccc3c(c2)C(F)(F)c2cc(-c4ccc5nc(C6C7CCC(C7)N6C(=O)C(NC(=O)OC)C(C)C)[nH]c5c4)ccc2-3)[nH]1)C(C)C
Reaction #159065
(1-{3-[6-(7-{2-[4-Cyano-1-(2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-9,9-difluoro-9H-fluoren-2-yl)-1H-benzoimidazol-2-yl]-2-aza-bicyclo[2.2.1]heptane-2-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC(C#N)CC1c1ncc(-c2ccc3c(c2)C(F)(F)c2cc(-c4ccc5nc(C6C7CCC(C7)N6C(=O)C(NC(=O)OC)C(C)C)[nH]c5c4)ccc2-3)[nH]1)C(C)C
Reaction #167014
(1-{3-[6-(7-{2-[4-Cyano-1-(2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-9,9-difluoro-9H-fluoren-2-yl)-1H-benzoimidazol-2-yl]-2-aza-bicyclo[2.2.1]heptane-2-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1ccc(-c2ncc(C(=O)NC3CC3)s2)cc1)N1CCC(CC(C)(C)C#N)(c2ccccc2)OC1=O
Reaction #193631
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(Sc2ccc(Br)cc2C(F)(F)F)CC1C(=O)NC1(C#N)CC1
Reaction #230015
DOI: 10.1039/C8SC04228D
COc1ccc(COCC2CC(S(=O)(=O)c3ccc(F)cc3Cl)CC2C(=O)NC2(C#N)CC2)cc1
Reaction #242049
DOI: 10.1039/C8SC04228D
CCC(CC)N1CCC(C#N)(NC(=O)C(CC2CCCCC2)NC2=NS(=O)(=O)c3ccccc32)C1
Reaction #243960
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C#N)CCC1CCN(c2nc(C)nc3c2c(C)c(C)n3-c2c(C)cc(Br)cc2C)CC1
Reaction #248228
DOI: 10.1039/C8SC04228D
N#CC1CC(S(=O)(=O)c2ccc(Br)cc2C(F)(F)F)CC1OC1CCOCC1
Reaction #263273
DOI: 10.1039/C8SC04228D
N#CC(CCc1cccs1)(Cn1cncn1)c1ccc(Cl)cc1
Reaction #290198
DOI: 10.1039/C8SC04228D
CC(=O)NCCC(C)(C)CC1NC(C(=O)NCCC(O)CO)C(c2cccc(Cl)c2F)C1(C#N)c1ccc(Cl)cc1F
Reaction #293673
DOI: 10.1039/C8SC04228D
CCCC(NC(c1ccc(-c2ccc(C(C)=O)cc2)cc1)C(F)(F)F)C(=O)NC1(C#N)CC1
Reaction #296986
DOI: 10.1039/C8SC04228D
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