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CSC1=CC(=C(C=C1)N)F

COC(=O)c1nn(C)c(=O)cc1Nc1ccc(SC)cc1F
Reaction #44237
desired product
Ausbeute 42.4%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCONC(=O)c1nn(C)c(=O)cc1Nc1ccc(SC)cc1F
Reaction #44238
desired product
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2cc(=O)n(C)nc2C(=O)NOCCO)c(F)c1
Reaction #44239
desired product
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nn(C)c(=O)c(C)c1Nc1ccc(SC)cc1F
Reaction #44245
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2c(C(=O)NOCCO)nn(C)c(=O)c2C)c(F)c1
Reaction #44246
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(=O)n(C)c1Nc1ccc(SC)cc1F
Reaction #44254
Methyl 2-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(=O)n(C)c1Nc1ccc(SC)cc1F
Reaction #44259
desired product
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCONC(=O)c1cc(F)c(=O)n(C)c1Nc1ccc(SC)cc1F
Reaction #44260
5-fluoro-2-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-N-(2-(vinyloxy)ethoxy)-1,6-dihydropyridine-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2c(C(=O)NOCCO)cc(F)c(=O)n2C)c(F)c1
Reaction #44261
5-fluoro-2-(2-fluoro-4-(methylthio)phenylamino)-N-(2-hydroxyethoxy)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-n2ncc(C#N)c2N)c(F)c1
Reaction #59657
pyrazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)N1CCC(Oc2ncnc3c2cnn3-c2ccc(S(C)(=O)=O)cc2F)CC1
Reaction #59660
product ( 6 )
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(N2CCN(C(=O)c3cc(S(C)(=O)=O)ccc3I)CC2)c(F)c1
Reaction #61037
[4-(2-Fluoro-4-methanesulfonyl-phenyl)-piperazin-1-yl]-(2-iodo-5-methanesulfonyl-phenyl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cc(F)c(N)c(Br)c1
Reaction #88217
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2c(C(=O)O)ccc(F)c2C=O)c(F)c1
Reaction #166208
title compound
Ausbeute 10.8%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2c(C(=O)O)ccc3[nH]ncc23)c(F)c1
Reaction #166209
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2c(C(=O)NOCCO)ccc3[nH]ncc23)c(F)c1
Reaction #166247
solid
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2c(C(=O)NOCCO)cc(F)c(=O)n2C)c(F)c1
Reaction #182953
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(N2CCc3c(OC4CCN(c5ncc(F)cn5)CC4)ncnc32)c(F)c1
Reaction #183550
DOI: 10.1039/C8SC04228D
CCOC(=O)c1nn(C)c(=O)c(C)c1Nc1ccc(SC)cc1F
Reaction #198147
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(Nc2ncnc3c2cnn3C2CCN(Cc3ccccc3)CC2)c(F)c1
Reaction #199090
DOI: 10.1039/C8SC04228D
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