部分構造検索

1393926

O=C(OCc1ccccc1)N1CCN(C(=O)[C@H](Cc2ccc(O)cc2)NS(=O)(=O)c2cccc3cnccc23)CC1
Reaction #5817
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #11905
desired product
収率 43.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1cc(F)c(F)cc1[N+](=O)[O-]
Reaction #11907
title compound
収率 16.7%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1CN(Cc2cccc(-c3ccnc(Cl)n3)c2)CCN1C(=O)OCc1ccccc1
Reaction #43224
4-[3-(2-Chloro-pyrimidin-4-yl)-benzyl]-2-cyano-piperazine-1-carboxylic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCN(C(=O)C2CCCCC2)CC1
Reaction #55357
2-(7-Chloro-1,8-naphthyridin-2-yl)-3-(4-cyclohexylcarbonylpiperazin-1-yl)carbonyloxy-isoindolin-1-one
収率 69.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCN(C(=O)C(F)(F)F)CC1
Reaction #55358
2-(7-Chloro-1,8-naphthyridin-2-yl)-3-(4-trifluoroacetylpiperazin-1-yl)carbonyloxy-isoindolin-1-one
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1ncccc1[N+](=O)[O-]
Reaction #56503
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1cccnc1[N+](=O)[O-]
Reaction #56504
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1nc(F)ccc1[N+](=O)[O-]
Reaction #56505
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N3CCN(C(=O)OCc4ccccc4)CC3)cc2)c2ccccc21
Reaction #69972
4-[4-(4-(Benzyloxycarbonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester
収率 78.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCN(c2ccc(N3CCNc4ccccc43)cc2)CC1
Reaction #69973
4-[4-(3,4-dihydro-2H-quinoxalin-1-yl)phenyl]piperazine-1-carboxylic acid benzyl ester
収率 99.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N3CCNCC3)cc2)c2ccccc21
Reaction #69974
4-(4-(piperazin-1-yl)phenyl)-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester
収率 95.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N3CCN(C(=O)OCc4ccccc4)CC3)cn2)c2ccccc21
Reaction #69984
4-[5-(4-(benzyloxycarbonyl)piperazin-1-yl)pyridin-2-yl]-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester
収率 74.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N3CCNCC3)cn2)c2ccccc21
Reaction #69985
4-(5-(piperazin-1-yl)pyridin-2-yl)-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester
収率 94.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(Cc2ccc(Br)cc2)CCN1C(=O)OCc1ccccc1
Reaction #71618
title compound
収率 84.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CN(C(=O)OC(C)(C)C)CCN1C(=O)OCc1ccccc1
Reaction #73089
1-benzyl 4-tert-butyl 2-methyl piperazine-1,2,4-tricarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #77315
desired product
収率 43.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(F)c(F)cc2N2CCNCC12
Reaction #77317
title compound
収率 16.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(=O)OCc2ccccc2)C(C(=O)O)C1
Reaction #82375
1-(benzyloxycarbonyl)-4-(tert.butoxycarbonyl)-2-piperazinecarboxylic acid
収率 37.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NC(=O)C1CN(C(=O)OC(C)(C)C)CCN1C(=O)OCc1ccccc1
Reaction #82376
1-(benzyloxycarbonyl)-4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamide
収率 56.4%DOI: 10.6084/m9.figshare.5104873.v1
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