部分構造検索

1167540

Cc1ccccc1C(=O)Nc1ccc(C(=O)N2CCCC(COC(=O)CN(C)C)c3cc(Cl)ccc32)cc1.Cl
Reaction #5683
5-[(2-dimethylaminoacetyloxy)methyl]-7-chloro-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine hydrochloride
収率 141.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc(CC(=O)O)c([N+](=O)[O-])c2)c1
Reaction #11633
(3′-methoxy-3-nitro-biphenyl-4-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc3c(c2)NC(=O)C3)c1
Reaction #52603
6-(3-methoxypheny)-2-oxindole
収率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1)NC(=O)C2
Reaction #52623
6-amino-2-oxindole
収率 101.3%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54062
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54063
title compound
収率 61.5%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54064
title compound
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54065
title compound
収率 101.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54066
title compound
収率 25.6%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54067
title compound
収率 92.8%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54068
title compound
収率 32.7%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54069
title compound
収率 140.4%DOI: 10.6084/m9.figshare.5104873.v1
COCOCC(O)c1cc2c(ncn2C)c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60288
desired product
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOCC(=O)c1cc2c(ncn2C)c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60289
desired product
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cnc2c(F)c(Nc3ccc(Br)cc3Cl)c(C(=O)CO)cc21
Reaction #60290
1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3-methyl-3H-benzoimidazol-5-yl]-2-hydroxy-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
OC(COCc1ccccc1)c1cc2[nH]cnc2c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60296
desired product
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COCc1ccccc1)c1cc2[nH]cnc2c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60297
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc(C(F)(F)F)c1CC(O)CO
Reaction #62710
2,3-dihydroxypropyl-3-aminobenzotrifluoride
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(C(F)(F)F)cc(=O)n(-c2c(F)cc(Cl)c(O)c2CC2(C)CO2)c1=O
Reaction #64097
1-[4-chloro-6-fluoro-3-hydroxy-2-(2,3-epoxy-2-methylpropyl)phenyl]-3-methyl-4-trifluoromethyl-1,2,3,6-tetrahydropyrimidine-2,6-dione
収率 88.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(Cl)c1Nc1ccccc1CC(=O)O
Reaction #74725
[o-(3-chloro-o-toluidino)-phenyl]-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
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