Propionyl chloride → (R)-2-propionamido-N-(1-(3-(trifluoromethyl)phenyl)ethyl)pyrimidine-4-carboxamide
反応式
[NH2:1][C:2]1[N:7]=[C:6]([C:8]([NH:10][C@@H:11]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([C:19]([F:22])([F:21])[F:20])[CH:14]=2)[CH3:12])=[O:9])[CH:5]=[CH:4][N:3]=1.[C:23](Cl)(=[O:26])[CH2:24][CH3:25]>>[C:23]([NH:1][C:2]1[N:7]=[C:6]([C:8]([NH:10][C@@H:11]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([C:19]([F:22])([F:20])[F:21])[CH:14]=2)[CH3:12])=[O:9])[CH:5]=[CH:4][N:3]=1)(=[O:26])[CH2:24][CH3:25]参加物
3
実験手順
The title compound is prepared from (R)-2-amino-N-(1-(3-(trifluoromethyl)phenyl)ethyl)pyrimidine-4-carboxamide (20 mg, 0.06 mmol, Step-1) and propionyl chloride (18 mg, 0.19 mmol) according to the procedure similar to that described in Step-2 of Example 8.
出典と根拠
- ORDレコード
- ord-ea9fab013df745ea8af9245b8cc71a0a
- 出典データセット
- uspto-grants-2016_04