Recherche de Sous-structure

14071

—
Reaction #7574
solid
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c([N+](=O)[O-])cc1O
Reaction #7576
4-fluoro-2-methyl-5-nitrophenol
Rendement 22.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c(N)cc1O
Reaction #7577
2-fluoro-5-hydroxy-4-methylaniline
Rendement 47.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7582
hydrochloride salt
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7583
hydrochloride salt
Rendement 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
Rendement 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
Rendement 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
Rendement 29.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c(O)cc1OCc1ccccc1
Reaction #7591
5-benzyloxy-2-fluoro-4-methylphenol
Rendement 27.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c(N)cc1OCc1ccccc1
Reaction #7592
5-benzyloxy-2-fluoro-4-methylaniline
Rendement 87.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c([N+](=O)[O-])cc1OCc1ccccc1
Reaction #7593
5-benzyloxy-2-fluoro-4-methylnitrobenzene
Rendement 80.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c([N+](=O)[O-])cc1O
Reaction #7594
2-fluoro-5-hydroxy-4-methylnitrobenzene
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7595
hydrochloride salt
Rendement 82.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7597
hydrochloride salt
Rendement 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
Rendement 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
Rendement 84.0%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
Cc1cc(F)c(Nc2ncnc3sc4c(c23)CCN(C(=O)/C=C/CN(C)C)C4)cc1O
Reaction #66894
5-({7-[(2E)-4-(Dimethylamino)but-2-enoyl]-5,6,7,8-tetrahydropyrido[4′,3′:4,5]thieno[2,3-d]-pyrimidin-4-yl}amino)-4-fluoro-2-methylphenol
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([N+](=O)[O-])c(F)cc1C
Reaction #160519
title compound
Rendement 81.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C#N)c1cc(C)c(OC)cc1[N+](=O)[O-]
Reaction #160520
title compound
Rendement 71.7%DOI: 10.6084/m9.figshare.5104873.v1
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