子结构搜索

1045131

COC(=O)c1c(Cl)cc([N+](=O)[O-])cc1Cl
Reaction #52989
methyl 2,6-dichloro-4-nitrobenzoate
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Cl)cc(Br)cc1Cl
Reaction #52990
4-bromo-2,6-dichlorobenzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Cl)cc(O)cc1Cl
Reaction #52991
2,6-dichloro-4-hydroxybenzoic acid methyl ester
收率 54.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Cl)cc(F)cc1Cl
Reaction #52992
2,6-dichloro-4-fluorobenzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC(=O)CCCCl)cc1Cl
Reaction #52994
4-(4-chlorobutyryl)amino-2-chlorobenzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Cl)cc(N)c(Br)c1Cl
Reaction #52999
2,6-dichloro-3-bromo-4-aminobenzoic acid methyl ester
收率 139.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC(=O)C(C)n2ccc(-c3cc(Cl)ccc3C#N)cc2=O)cc1Cl
Reaction #84911
Methyl 2-chloro-4-({2-[4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]propanoyl}amino)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)Nc1ccc(C(=O)O)c(Cl)c1)n1ccc(-c2cc(Cl)ccc2C#N)cc1=O
Reaction #85240
2-Chloro-4-({2-[4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]propanoyl}amino)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(Cl)cc(C(=O)Nc2ccc(C(=O)OC)c(Cl)c2)cc1Cl
Reaction #91000
Methyl 4-(3,5-dichloro-4-ethoxybenzamido)-2-chlorobenzoate
收率 39.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)OCc2ccccc2)c(Cl)cc1Nc1ncc(Cl)c(Oc2cccc3c2C(=O)N(C)C3)n1
Reaction #168537
benzyl 2-chloro-4-[5-chloro-4-(2-methyl-3-oxo-2,3-dihydro-1H-isoindol-4-yloxy)-pyrimidin-2-ylamino]-5-methoxy-benzoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)c(Cl)cc1Nc1ncc(Cl)c(Oc2cccc3c2C(=O)N(C)C3)n1
Reaction #168538
2-chloro-4-[5-chloro-4-(2-methyl-3-oxo-2,3-dihydro-1H-isoindol-4-yloxy)-pyrimidin-2-ylamino]-5-methoxy-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)cc1Cl
Reaction #192283
DOI: 10.1039/C8SC04228D
COC(=O)c1c(Cl)cc(O)cc1Cl
Reaction #211653
DOI: 10.1039/C8SC04228D
COC(=O)c1c(Cl)cc([N+](=O)[O-])cc1Cl
Reaction #281776
DOI: 10.1039/C8SC04228D
COC(=O)c1c(Cl)cc(NS(C)(=O)=O)cc1Cl
Reaction #358507
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Cl)cc(N)cc1Cl
Reaction #378046
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(NC(=O)c2ccc3c(c2)N(S(=O)(=O)c2cccc(Cl)c2)CC3)cc1Cl
Reaction #391441
DOI: 10.1039/C8SC04228D
COC(=O)c1c(Cl)cc(I)cc1Cl
Reaction #393420
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(NC(=O)[C@@H]2N[C@@H](CC(C)(C)C)[C@@]3(C(=O)Nc4cc(Cl)ccc43)[C@H]2c2cccc(Cl)c2F)cc1Cl
Reaction #504373
rac-2-chloro-4-{[(2′S,3′R,4′S,5′R)-6-chloro-4′-(3-chloro-2-fluoro-phenyl)-2′-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3′-pyrrolidine]-5′-carbonyl]-amino}-benzoic acid methyl ester
收率 32.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CC1NC(C(=O)O)C(c2cccc(Cl)c2F)C12C(=O)Nc1cc(Cl)ccc12
Reaction #504561
rac-(2′S,3′R,4′S,5′R)-6-chloro-4′-(3-chloro-2-fluoro-phenyl)-2′-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3′-pyrrolidine]-5′-carboxylic acid
收率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
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