Hydrochloric Acid → HCID 59536813、化合物
反応式
[CH2:1]([NH:4][C:5]([NH:7][NH:8][C:9](=O)[C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][C:11]=1[Br:17])=[O:6])[CH:2]=[CH2:3].[OH-].[Na+].Cl>>[CH2:1]([N:4]1[C:9]([C:10]2[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][C:11]=2[Br:17])=[N:8][NH:7][C:5]1=[O:6])[CH:2]=[CH2:3]参加物
4
実験手順
Of the compound from Example 163A, 11.3 g (33.98 mmol) were taken up in 61 ml (183.47 mmol) of 3M aqueous sodium hydroxide solution and heated under reflux for 36 h. The batch was then cooled, the fine precipitate was removed by filtration, and the filtrate was admixed, with ice cooling, with 28 ml (169.88 mmol) of half-concentrated hydrochloric acid to a pH of 10. The batch was filtered with suction and the product was dissolved out of the precipitate using methanol. The methanol was removed on a rotary evaporator. The residue was dried in an HV. This gave 9.78 g (69% of theory) of the title compound in 75% purity.
後処理
- temperatureheated
- temperatureunder reflux for 36 h
- temperatureThe batch was then cooled
- customthe fine precipitate was removed by filtration
- filtrationThe batch was filtered with suction
- dissolutionthe product was dissolved out of the precipitate
- customThe methanol was removed on a rotary evaporator
- customThe residue was dried in an HV
出典と根拠
- ORDレコード
- ord-4c4615ca118b4ed6bb8e63aa027fcbe5
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08202895B2
反応ノート
読み込み中…