部分構造検索

COC(=O)CCCc1ccc(N)cc1

Cn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(Nc3ccc(CCCC(=O)O)cc3)nc21
Reaction #3314
pure acid
収率 34.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCc1ccc(N)cc1.Cl
Reaction #40269
methyl 4-(4-aminophenyl)butyrate hydrogen chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cl)cc1-c1cc(Nc2ccc(CCCC(=O)O)cc2)nc(N)n1
Reaction #56891
title compound
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(C)C(=O)c1ccc2c(c1)SCC(=O)N2C
Reaction #63463
Methyl 4-(3,4-dihydro-4-methyl-3-oxo-1,4[2H]-benzothiazin-7-yl)-3-methyl-4-oxobutyrate
DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(=O)NN=C1c1ccc2c(c1)SCC(=O)N2C
Reaction #63465
named compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C(=O)C(c2ccc(N3CCOCC3)cc2)N(c2ccc3[nH]cnc3c2)C1=O
Reaction #70030
Ethyl 1-(1H-benzo[d]imidazol-5-yl)-5-(4-morpholinophenyl)-2,4-dioxopyrrolidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(=O)N(c2ccc3[nH]cnc3c2)C1c1ccc(N2CCOCC2)cc1
Reaction #70046
1-(1H-Benzo[d]imidazol-5-yl)-5-(4-morpholinophenyl)pyrrolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCc2ccc(N)cc2O1
Reaction #77737
title compound
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1)OC(CO)CC2
Reaction #77738
title compound
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCc2ccc(NC=O)cc2O1
Reaction #77742
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc2c(c1)OC(CO)CC2
Reaction #77743
title compound
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc(C2CCCCC2(CC(=O)OC)C(=O)C2(CC(=O)OC)CCCCC2c2ccc(NC)c(NC(=O)COc3ccc(C#N)cc3)c2)cc1NC(=O)COc1ccc(C#N)cc1
Reaction #78606
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC(CC(=O)c1ccc(N)cc1)C(=O)OCC
Reaction #187807
DOI: 10.1039/C8SC04228D
Nc1ccc2c(c1)OC(CO)CC2
Reaction #191034
DOI: 10.1039/C8SC04228D
COC(=O)CC1Cc2ccc(NC(=O)CCNC(=O)OC(C)(C)C)cc2CN(C)C1=O
Reaction #191564
DOI: 10.1039/C8SC04228D
C=CCNc1ccc(C(=O)CCC(=O)O)cc1
Reaction #191638
DOI: 10.1039/C8SC04228D
O=C1CC(=O)N(c2ccc3[nH]cnc3c2)C1c1ccc(N2CCOCC2)cc1
Reaction #203392
DOI: 10.1039/C8SC04228D
CC12CCC3c4ccc(OCc5ccccc5)cc4CCC3C1CCC2OCCOC(=O)CCCc1ccc(N(CCCl)CCCl)cc1
Reaction #204689
DOI: 10.1039/C8SC04228D
COC(=O)CCC(=O)c1ccc([N+](=O)[O-])c(OCc2ccccc2)c1
Reaction #207635
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCOC(=O)CCC(=O)c1ccc(N)cc1
Reaction #211874
DOI: 10.1039/C8SC04228D
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