1,2,3-Trifluoro-5-methoxybenzene → (4-Amino-2-ethylsulfanyl-pyrimidin-5-yl)-(2,3,4-trifluoro-6-methoxy-phenyl)-methanone
Reaction equation
CON(C)[C:4]([C:6]1[C:7]([NH2:15])=[N:8][C:9]([S:12][CH2:13][CH3:14])=[N:10][CH:11]=1)=[O:5].[F:17][C:18]1[CH:19]=[C:20]([O:26][CH3:27])[CH:21]=[C:22]([F:25])[C:23]=1[F:24]>>[NH2:15][C:7]1[C:6]([C:4]([C:19]2[C:20]([O:26][CH3:27])=[CH:21][C:22]([F:25])=[C:23]([F:24])[C:18]=2[F:17])=[O:5])=[CH:11][N:10]=[C:9]([S:12][CH2:13][CH3:14])[N:8]=1Participants
3
Procedure
The compound was prepared from 4-amino-2-ethylsulfanyl-pyrimidine-5-carboxylic acid methoxy-methyl-amide, Example 1, and 3,4,5-trifluoroanisole (Aldrich) in an analogous manner as described in Example 169.
Sources & evidence
- ORD record
- ord-0ac1fb67bd8c49b08816b8087d6bfa61
- Source dataset
- uspto-grants-2009_11