Acetamide → HCID 67510009, compound
Reaction equation
Cl[C:2]1[N:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[CH:5]=[C:4]([CH3:12])[N:3]=1.[C:13]([NH2:16])(=[O:15])[CH3:14]>>[C:13]([NH:16][C:2]1[N:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[CH:5]=[C:4]([CH3:12])[N:3]=1)(=[O:15])[CH3:14]Participants
3
Procedure
The title compound is prepared in 68% yield (0.76 g, a yellow solid) from methyl 2-chloro-6-methylpyrimidine-4-carboxylate (1.0 g, 5.4 mmol) and acetamide by the similar manner in Step-1 of Carboxylic acid-4.
Sources & evidence
- ORD record
- ord-b9f80a979b164d81b0d23f6d7f27329c
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09302991B2
Reaction notes
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