2-Bromo-4-fluorobenzotrifluoride → HCID 21070591, compound
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].Br[C:18]1[CH:23]=[C:22]([F:24])[CH:21]=[CH:20][C:19]=1[C:25]([F:28])([F:27])[F:26]>>[NH2:15][C:7]1[C:6]([C:4]([C:20]2[CH:21]=[C:22]([F:24])[CH:23]=[CH:18][C:19]=2[C:25]([F:26])([F:27])[F:28])=[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 2-bromo-4-fluoro-1-trifluoromethyl-benzene (Aldrich) in an analogous manner as described in Example 169.
Sources & evidence
- ORD record
- ord-5472311f5eac4e54ab5732f6f5327f2e
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07157455B2
Reaction notes
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