反応式
[OH:1][N:2]=[C:3](Cl)[C:4]1[C:8]([NH:9][CH2:10][CH2:11][O:12][CH3:13])=[N:7][O:6][N:5]=1.FC(F)(F)C(O)=O.[Cl:22][C:23]1[CH:24]=[C:25]([CH2:28][NH2:29])[O:26][CH:27]=1>>[Cl:22][C:23]1[CH:24]=[C:25]([CH2:28][NH:29][C:3]([C:4]2[C:8]([NH:9][CH2:10][CH2:11][O:12][CH3:13])=[N:7][O:6][N:5]=2)=[N:2][OH:1])[O:26][CH:27]=1参加物
3
実験手順
The desired compound was prepared according to the procedure of Example 20, step C, using N-hydroxy-4-(2-methoxyethylamino)-1,2,5-oxadiazole-3-carbimidoyl chloride and 1-(4-chloro-2-furyl)methanamine trifluoroacetate as the starting material in quantitative yield. LCMS calculated for C11H15ClN5O4 (M+H)+: m/z=316.0.
出典と根拠
- ORDレコード
- ord-7c8d99fa94ad48eda0f89911c62e16ed
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08822511B2
関連ノート
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