子结构搜索

712884

O=C(O)C1CCN(C(=O)c2ccccc2SSc2ccccc2C(=O)N2CCC(C(=O)O)CC2)CC1
Reaction #3834
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)C(C)(C)C)CC1
Reaction #40674
20a
收率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CN1CCC(CO)CC1
Reaction #40675
desired product
收率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)c2cccc(Cl)c2)CC1
Reaction #48544
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCN(C(=O)c2cnc(NC34CC5CC(CC(C5)C3)C4)nc2C(F)(F)F)CC1
Reaction #67079
1-{[2-(adamantan-1-ylamino)-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}piperidine-4-carboxylic acid
收率 91.7%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1CCN(C(=O)c2cnc(NC34CC5CC(CC(C5)C3)C4)nc2C(F)(F)F)CC1
Reaction #67080
1-{[2-(adamantan-1-ylamino)-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}piperidine-4-carboxamide
收率 68.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(C)C
Reaction #78071
diisopropyl ether
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CNC(=O)c2c(C)nc3c(OCC4CCCCC4)cccn23)CCN(C(C)=O)CC1
Reaction #92743
methyl 1-acetyl-4-[({[8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridin-3-yl]carbonyl}amino)methyl]piperidine-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)c2cccc(Nc3nc(Cl)ncc3F)c2)CC1
Reaction #158499
2-chloro-N4-[3-[[4-(ethoxycarbonyl)piperidino]carbonyl]phenyl]-5-fluoro-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)c2cccc(N)c2)CC1
Reaction #158513
3-[4-(ethoxycarbonyl)piperidinocarbonyl]aniline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)c2cccc(Nc3ncc(F)c(Nc4cccc(O)c4)n3)c2)CC1
Reaction #158803
N2-[3-[[4-(ethoxycarbonyl)piperidino]carbonyl]phenyl]-5-fluoro-N4-(3-hydroxyphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)c2cccc(Nc3nc(Nc4cccc(O)c4)ncc3F)c2)CC1
Reaction #158804
N4-[3-[[4-(ethoxycarbonyl)piperidino]carbonyl]phenyl]-5-fluoro-N2-(3-hydroxyphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)c2cccc(Nc3nc(Cl)ncc3F)c2)CC1
Reaction #163609
2-chloro-N4-[3-[[4-(ethoxycarbonyl)piperidino]carbonyl]phenyl]-5-fluoro-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)c2cccc(N)c2)CC1
Reaction #163623
3-[4-(ethoxycarbonyl)piperidinocarbonyl]aniline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)c2cccc(Nc3ncc(F)c(Nc4cccc(O)c4)n3)c2)CC1
Reaction #163914
N2-[3-[[4-(ethoxycarbonyl)piperidino]carbonyl]phenyl]-5-fluoro-N4-(3-hydroxyphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)c2cccc(Nc3nc(Nc4cccc(O)c4)ncc3F)c2)CC1
Reaction #163915
N4-[3-[[4-(ethoxycarbonyl)piperidino]carbonyl]phenyl]-5-fluoro-N2-(3-hydroxyphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)c2cccn2Cc2ccc(Cl)cc2)CC1
Reaction #170776
title compound
收率 75.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCN(C(=O)c2cccn2Cc2ccc(F)cc2)CC1
Reaction #170777
title compound
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)c2cc3ccccc3n2Cc2ccc(Cl)cc2)CC1
Reaction #170779
Ethyl 1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccccc1)C1CCN(C(=O)c2cc3ccccc3n2Cc2ccc(F)cc2)CC1
Reaction #170783
N-benzyl-1-(1-(4-fluorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
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