Trimethyl orthobeznoate → HCID 10514375、化合物
反応式
[NH2:1][C:2]1[N:6]([C:7]([NH:9][CH3:10])=[S:8])[N:5]=[CH:4][N:3]=1.CO[C:13](OC)(OC)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[CH3:10][N:9]1[C:7](=[S:8])[N:6]2[N:5]=[CH:4][N:3]=[C:2]2[N:1]=[C:13]1[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1参加物
3
実験手順
The synthesis method of Example 96 was applied. The compound (1.50 g) obtained in Example 29 and trimethylorthobenzoate (5.0 ml) were used. The mixture was reacted at 150° C. for 2 hours. The resulting crystals were collected by filtration and purified by a method similar to the method of Example 98, whereby crystals (1.53 mg) were obtained (yield 66%). The crystals were recrystallized from methanol to give colorless transparent plate crystals.
後処理
- customThe synthesis method of Example 96
- customThe mixture was reacted at 150° C. for 2 hours
- filtrationThe resulting crystals were collected by filtration
- custompurified by a method similar to the method of Example 98
出典と根拠
- ORDレコード
- ord-c16ddba7f3e64e3a9d501a12477c5174
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05750545
反応ノート
読み込み中…