Hydrogen Bromide → HCID 19850133、化合物
反応式
[F:1][C:2]1[CH:7]=[C:6]([CH2:8][CH2:9][NH:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][NH:17][CH2:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:5]=[CH:4][C:3]=1[OH:26].[BrH:27]>[PH2](O)=O>[BrH:27].[BrH:27].[F:1][C:2]1[CH:7]=[C:6]([CH2:8][CH2:9][NH:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][NH:17][CH2:18][CH2:19][C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH:5]=[CH:4][C:3]=1[OH:26]参加物
4
実験手順
The product from step (b) (1.8 g) in 48% hydrobromic acid (18 ml) containing hypophosphorous acid (10 drops) was boiled at reflux under nitrogen for 5.5 hr. The solid which separated on cooling the solution was collected and recrystallised from water giving the dihydrobromide salt of the title compound as colourless needles (1.3 g) mp 240.5°-242.5°.
後処理
- temperatureat reflux under nitrogen for 5.5 hr
- customThe solid which separated
- temperatureon cooling the solution
- customwas collected
- customrecrystallised from water giving the dihydrobromide salt of the title compound as colourless needles (1.3 g) mp 240.5°-242.5°
出典と根拠
- ORDレコード
- ord-867d94ca17a6452db859bbe8c9a780c0
- 出典データセット
- uspto-grants-1988_12
- 特許番号
- US04791216
反応ノート
読み込み中…