部分構造検索

93421

CN1CCC(Oc2ccc(C#N)cc2C(F)(F)F)CC1
Reaction #42042
objective compound
収率 64.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1ccc2c(C#N)cc(C(=O)N[C@@H](Cc3cc(F)cc(F)c3)[C@H](O)CNCc3cccc(CC)c3)cc21
Reaction #42460
title compound
収率 70.3%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)C#Cc1cccc(C#N)c1
Reaction #45375
solid
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N(CCO)CCO)c(C(F)(F)F)c1
Reaction #51890
3-trifluoromethyl-4-[bis(2-hydroxyethyl)amino]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(CC1CCC1)c1cccc(C#N)c1
Reaction #58666
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc2[nH]c(COCC[Si](C)(C)C)nc2c(F)c1Nc1ccc(C#N)cc1C
Reaction #60321
desired product
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(C(F)(F)F)cc2C#N)CC1
Reaction #60930
Title compound
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C(F)(F)F)ccc1N1CCN(C(=O)c2cc([N+](=O)[O-])ccc2N2CCOCC2)CC1
Reaction #60985
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CCC(c1cccc(C#N)c1)n1cc(-c2ncnc3c2ccn3COCC[Si](C)(C)C)cn1
Reaction #69271
3-{1-[4-(7-{[2-(trimethylsilyl)ethoxy]-methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]but-3-yn-1-yl}benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
C#CCC(c1cccc(C#N)c1)n1cc(-c2ncnc3c2ccn3COCC[Si](C)(C)C)cn1
Reaction #73302
3-{1-[4-(7-{[2-(trimethylsilyl)ethoxy]-methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]but-3-yn-1-yl}benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccc2c(c1)nc(CNc1ccc(C(=N)N)cc1CC)n2C)c1ccccc1.Cl
Reaction #78629
1-Methyl-2-[N-(4-amidino-2-ethylphenyl)aminomethyl]benzimidazol-5-yl-carboxylic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amide hydrochloride
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O.CC(=O)O.CN1CCN(C2CCC(n3cc(-c4ccc(Oc5ccccc5)c(C#N)c4)c4c(N)ncnc43)CC2)CC1
Reaction #79848
5-{4-amino-7-[4-(4-methylpiperazino)cyclohexyl]-7H-pyrrolo[2,3-d]pyrimidin-5-yl}-2-phenoxybenzonitrile bisacetate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cn([C@H]3CC[C@H](N4CCNCC4C)CC3)c3ncnc(Cl)c23)ccc1Oc1ccccc1
Reaction #79850
title compound
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN([C@H]2CC[C@H](n3cc(-c4ccc(Oc5ccccc5)c(F)c4)c4c(Cl)ncnc43)CC2)CC1
Reaction #79858
title compound
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cn([C@H]3CC[C@H](N4CCN(C)CC4)CC3)c3ncnc(Cl)c23)ccc1Oc1ccccc1
Reaction #79861
title compound
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=NO)c1cc(F)cc(C(F)(F)F)c1
Reaction #87541
desired product
収率 40.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)ccc1N1CCN(C(=O)[C@H]2CCN(/C(=N/C#N)N3CCCCC3)C[C@@H]2C(=O)NO)CC1
Reaction #89765
(3R,4S)-1-[(E)-(cyanoimino)(piperidin-1-yl)methyl]-4-[4-(4-cyano-2-methylphenyl)piperazin-1-yl]carbonyl-N-hydroxypiperidine-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1coc([C@H]2C[C@H]3CSC(NC(=O)c4ccccc4)=N[C@@]3(c3cc(C#N)ccc3F)CO2)n1
Reaction #155604
N-[(4aR,6R,8aS)-8a-(5-cyano-2-fluorophenyl)-6-(4-methyl-1,3-oxazol-2-yl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1coc([C@H]2C[C@H]3CSC(N)=N[C@@]3(c3cc(C#N)ccc3F)CO2)n1
Reaction #155605
product
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc([C@H]2C[C@H]3CSC(NC(=O)c4ccccc4)=N[C@@]3(c3cc(C#N)ccc3F)CO2)cn1
Reaction #155610
N-[(4aR,6R,8aS)-8a-(5-cyano-2-fluorophenyl)-6-(1-methyl-1H-pyrazol-4-yl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
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