Участвует в 51 реакциях

795840

Cn1cc(C(=O)O)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #44183
desired product
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cn1cc(C(=O)NOCC2CC2)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #44184
clean desired product
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=COCCONC(=O)c1cn(C)c(=O)cc1Nc1ccc(Br)cc1F
Reaction #44185
clean desired product
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cn1cc(C(N)=O)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #44187
clean desired product
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cn1cc(C(=O)NOCCO)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #222572
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1cc(C(=O)O)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #378976
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cn1cc(C(=O)O)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #509029
desired product
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cn1cc(C(=O)NOCC2CC2)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #509030
clean desired product
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C=COCCONC(=O)c1cn(C)c(=O)cc1Nc1ccc(Br)cc1F
Reaction #509031
clean desired product
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cn1cc(C(N)=O)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #509033
clean desired product
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cn1cc(C(=O)O)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #509937
desired product
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cn1cc(C(=O)NOCC2CC2)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #509938
clean desired product
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C=COCCONC(=O)c1cn(C)c(=O)cc1Nc1ccc(Br)cc1F
Reaction #509939
clean desired product
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cn1cc(C(N)=O)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #509941
clean desired product
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cn1cc(C(=O)NCCCO)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #902557
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cn1cc(C(=O)Oc2c(F)c(F)c(F)c(F)c2F)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #918472
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cn1cc(C(=O)NOCCO)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #1004933
4-(4-bromo-2-fluoroanilino)-N-(2-hydroxyethoxy)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxamide
Выход 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
Cn1cc(C(=O)NCCCO)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #1004934
4-(4-bromo-2-fluoroanilino)-N-(3-hydroxypropyl)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxamide
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
Cn1cc(C(=O)Oc2c(F)c(F)c(F)c(F)c2F)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #1004935
2,3,4,5,6-pentafluorophenyl 4-(4-bromo-2-fluoroanilino)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxylate
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
Cn1cc(C(=O)NOCC2CC2)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #1039930
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
Страница 1Далее