子结构搜索

17057

COC(=O)c1cc(F)c(O)cc1OC
Reaction #1769
methyl 5-fluoro-4-hydroxy-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(O[C@@H](C)c2ccncc2)cc1OC
Reaction #1796
methyl 5-fluoro-2-methoxy-4-[1-(S)-(4-pyridyl)ethoxy]benzoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O[C@@H](C)c2ccncc2)c(F)cc1C(=O)O
Reaction #1797
5-fluoro-2-methoxy-4-[1-(S)-(4-pyridyl)ethoxy]benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7574
solid
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c(N)cc1O
Reaction #7577
2-fluoro-5-hydroxy-4-methylaniline
收率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7582
hydrochloride salt
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7583
hydrochloride salt
收率 27.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Nc3cc(O)c(C)cc3F)cnnc2cc1OCc1csc(C)n1.Cl
Reaction #7584
4-(2-fluoro-5-hydroxy-4-methylanilino)-6-methoxy-7-[(2-methylthiazol-4-yl)methoxy]cinnoline hydrochloride
收率 89.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Nc3cc(O)c(C)cc3F)cnnc2cc1OCc1nccn1C.Cl
Reaction #7586
4-(2-fluoro-5-hydroxy-4-methylanilino)-6-methoxy-7-[(1-methylimidazol-2-yl)methoxy]cinnoline hydrochloride
收率 79.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Nc3cc(O)c(C)cc3F)cnnc2cc1OCc1ccncc1.Cl
Reaction #7588
4-(2-fluoro-5-hydroxy-4-methylanilino)-6-methoxy-7-(4-pyridylmethoxy)cinnoline hydrochloride
收率 29.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7595
hydrochloride salt
收率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7597
hydrochloride salt
收率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c(Nc2cnnc3ccc(Cl)cc23)cc1O.Cl
Reaction #7598
6-chloro-4-(2-fluoro-5-hydroxy-4-methylanilino)cinnoline hydrochloride
收率 95.8%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccc2c(Nc3cc(O)c(C)cc3F)cnnc2c1.Cl
Reaction #7601
4-(2-fluoro-5-hydroxy-4-methylanilino)-7-(2-methoxyethoxy)cinnoline hydrochloride
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCN(CCc1cc(F)ccc1O)Cc1ccc(C(=O)OC)cc1
Reaction #8227
Methyl 4-({(5-methoxy-5-oxopentyl)[2-(5-fluoro-2-hydroxyphenyl)-ethyl]amino}methyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)cc1CC(O)(C1CCOCC1)C1CNCCO1.Cl
Reaction #58605
compound 52b
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c(Nc2ncnc3sc4c(c23)CCNC4)cc1O.Cl
Reaction #66836
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(F)cc1-c1ccn(-c2ccnc3[nH]ccc23)n1
Reaction #69199
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(F)cc1-c1ccn(-c2ccnc3[nH]ccc23)n1
Reaction #73233
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cc(F)ccc2OC)cc1)NC(=O)CCC(=O)OC(C)(C)C
Reaction #158007
(R)-tert-butyl 4-(4-ethoxy-1-(5′-fluoro-2′-methoxybiphenyl-4-yl)-4-oxobutan-2-ylamino)-4-oxobutanoate
DOI: 10.6084/m9.figshare.5104873.v1
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