Acetyl chloride → HCID 67510224, compound
Reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([C:8]([NH:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([O:18][C:19]([F:22])([F:21])[F:20])[CH:13]=2)=[O:9])[CH:5]=[CH:4][N:3]=1.[C:23](Cl)(=[O:25])[CH3:24]>>[C:23]([NH:1][C:2]1[N:7]=[C:6]([C:8]([NH:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([O:18][C:19]([F:22])([F:20])[F:21])[CH:13]=2)=[O:9])[CH:5]=[CH:4][N:3]=1)(=[O:25])[CH3:24]Participants
3
Procedure
The title compound is prepared from 2-amino-N-(3-(trifluoromethoxy)benzyl)pyrimidine-4-carboxamide (15 mg, 0.05 mmol, Step-1) and acetyl chloride (11 mg, 0.14 mmol) according to the procedure similar to that described in Step-2 of Example 8.
Sources & evidence
- ORD record
- ord-9f8fe324af0649d2bcd9733b7d5e6620
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09302991B2
Reaction notes
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