反応式
[CH3:1][C:2]1[N:3]=[C:4]([NH2:7])[S:5][CH:6]=1.O.O.O.[F:11][C:12]([F:20])([F:19])[C:13]([C:15]([F:18])([F:17])[F:16])=[O:14]>>[NH2:7][C:4]1[S:5][C:6]([C:13]([OH:14])([C:15]([F:18])([F:17])[F:16])[C:12]([F:20])([F:19])[F:11])=[C:2]([CH3:1])[N:3]=1参加物
3
実験手順
The title compound was prepared from commercially available of 4-methylthiazol-2-amine (Aldrich) and hexafluoroacetone trihydrate (Aldrich) using the procedure described in European Journal of Organic Chemistry, (21), 4286-4291; 2003. MS (ESI+) m/z 281 (M+H)+.
出典と根拠
- ORDレコード
- ord-4e9ba0fcdf1c410fa7d97c2d7f3256d0
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08841334B2
関連ノート
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