Hydrazine hydrate (1:1) → 6-Bromoquinazoline-4-carboxylic acid hydrazide
反応式
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][N:6]=[C:5]2[C:12]([O:14]C)=O.O.[NH2:17][NH2:18]>CO>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][N:6]=[C:5]2[C:12]([NH:17][NH2:18])=[O:14]参加物
4
実験手順
A mixture of 961 mg methyl 6-bromoquinazoline-4-carboxylate (compound in Production Example 413), 0.9 mL hydrazine monohydrate and 70 mL methanol was stirred at room temperature for 30 minutes, and the precipitated crystals were collected by filtration. The filtrate was evaporated to give additional crystals. The title compound, 838 mg in total, was obtained as pale yellow crystals.
後処理
- filtrationthe precipitated crystals were collected by filtration
- customThe filtrate was evaporated
- customto give additional crystals
出典と根拠
- ORDレコード
- ord-b96e73a1e56e4329afd9d3fefcac5524
- 出典データセット
- uspto-grants-2006_07
- 特許番号
- US07074801B1
反応ノート
読み込み中…