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621594

C=COCCONC(=O)c1cn(C)c(=O)cc1Nc1ccc(Br)cc1F
Reaction #44185
clean desired product
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(C(=O)NOCCO)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #44186
clean desired product
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2c(C(=O)NOCCO)ccc(=O)n2C)c(F)c1
Reaction #44218
pure desired product
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(Nc2ccc(Br)cc2F)c(C(=O)NOCCO)ccc1=O
Reaction #44219
pure desired product
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCONC(=O)c1nn(C)c(=O)cc1Nc1ccc(SC)cc1F
Reaction #44238
desired product
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2cc(=O)n(C)nc2C(=O)NOCCO)c(F)c1
Reaction #44239
desired product
Выход 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2c(C(=O)NOCCO)nn(C)c(=O)c2C)c(F)c1
Reaction #44246
title compound
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCONC(=O)c1nn(C)c(=O)c(C)c1Nc1ccc(I)cc1F
Reaction #44250
4-(2-fluoro-4-iodophenylamino)-1,5-dimethyl-6-oxo-N-(2-(vinyloxy)ethoxy)-1,6-dihydropyridazine-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)NOCCO)c(Nc2ccc(Br)cc2F)n(C)c1=O
Reaction #44252
pure desired product
Выход 94.0%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
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCONC(=O)c1cc2c(ncn2C)c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60260
desired product
Выход 90.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cnc2c(F)c(Nc3ccc(Br)cc3Cl)c(C(=O)NOCCO)cc21
Reaction #60261
6-(4-bromo-2chloro-phenylamino)-7-fluoro-3-methyl-3H-benzoimidazole-5-carboxylic acid (2-hydroxy-ethoxy)-amide
Выход 102.4%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCONC(=O)c1cc2c(ncn2CC2CCCCO2)c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60278
pure desired product
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NOCCO)c1cc2c(ncn2CC2CCCCO2)c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60279
pure desired product
Выход 92.3%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCONC(=O)c1cc2c(ncn2C)c(Cl)c1Nc1ccc(Br)cc1Cl
Reaction #60317
pure material
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCONC(=O)c1ccc2c(cnn2S(=O)(=O)c2ccc(C)cc2)c1Nc1ccc(I)cc1F
Reaction #166230
title compound
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NOCCO)c1ccc2[nH]ncc2c1Nc1ccc(I)cc1F
Reaction #166231
title compound
Выход 10.0%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCONC(=O)c1ccc2[nH]ncc2c1Nc1ccc(I)cc1F
Reaction #166232
title compound
Выход 71.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #166233
solid
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1
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