Substructure Search

458537

COc1ccc2nc(-c3cccc(C)c3)ccc2c1
Reaction #68709
2-(3-methylphenyl)-6-methoxyquinoline
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(Sc3ccc(N)cc3)ccc2c1
Reaction #83346
2-(4-aminophenylthio)-6-methoxyquinoline
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-c2nc3ccc(OC)cc3cc2C)cc1
Reaction #84056
methyl 4-(6-methoxy-3-methylquinolin-2-yl)benzoate
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(-c3ccc(-c4nnn[nH]4)cc3)c(C)cc2c1
Reaction #84058
desired product
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(-c2ccc3cc(O)ccc3n2)cc1
Reaction #84060
4-(6-hydroxyquinolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2nc(-c3ccc(-c4nnn[nH]4)cc3)ccc2c1
Reaction #84061
2-(4-(1H-tetrazol-5-yl)phenyl)quinolin-6-ol
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(c2ccc3cc(OC)ccc3n2)CC1
Reaction #84062
ethyl 4-(6-methoxyquinolin-2-yl)cyclohexanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(-c3ccc(C(=O)O)cc3Cl)ccc2c1
Reaction #84063
3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(-c3ccc(C#N)cc3)cc(Cl)c2c1
Reaction #84066
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(-c3ccc(C(=O)O)cc3)c(Cl)cc2c1
Reaction #84076
4-(3-chloro-6-methoxyquinolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC=C(c2nc3ccc(OC)cc3cc2Cl)CC1
Reaction #84088
ethyl 4-(3-chloro-6-methoxyquinolin-2-yl)cyclohex-3-enecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(-c2cc(F)c3cc(O)ccc3n2)c(Cl)c1
Reaction #84090
3-chloro-4-(4-fluoro-6-hydroxyquinolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2ccc3cc(O)ccc3n2)s1
Reaction #84091
5-(6-hydroxyquinolin-2-yl)thiophene-2-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(-c2cc(F)c3cc(O)ccc3n2)c(F)c1
Reaction #84093
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCN(c2nc3ccc(OC)cc3cc2C(F)(F)F)CC1
Reaction #84094
product
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-c2ccc3cc(OC)ccc3n2)cc1
Reaction #84097
product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-c2ccc3cc(OC)ccc3n2)c(N)c1
Reaction #84099
product
Yield 19.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2nc(Cl)cc(F)c2c1
Reaction #84101
product
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(Cl)c(C#N)cc2c1
Reaction #84104
product
Yield 38.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(Cl)ccc2c1
Reaction #84110
2-chloro-6-methoxyquinoline
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
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