反応式
[CH3:1][NH:2][C@@H:3]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[C@H:6]([C:13]2[CH:14]=[CH:15][C:16]([Cl:20])=[C:17]([Cl:19])[CH:18]=2)[CH2:5][CH2:4]1.[ClH:21]>C(O)CC>[CH3:1][NH:2][C@@H:3]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[C@H:6]([C:13]2[CH:14]=[CH:15][C:16]([Cl:20])=[C:17]([Cl:19])[CH:18]=2)[CH2:5][CH2:4]1.[ClH:21]参加物
4
実験手順
A solution of 50 g free sertraline base in 100 ml of n-propanol was added dropwise over a period of about 30 minutes at ambient temperature onto 100 ml of n-propanol containing 13 ml of 37% aqueous hydrochloric acid. About 10 minutes after the end of the addition a white crystalline solid starts to form. Stirring is maintained for 1 hour then the solid is filtered and washed. It is dried under vacuum. 47.5 g of sertraline hydrochloride form II are obtained in a 85% yield.
後処理
- additionAbout 10 minutes after the end of the addition a white crystalline solid starts
- customto form
- temperatureis maintained for 1 hour
- filtrationthe solid is filtered
- washwashed
- customIt is dried under vacuum
出典と根拠
- ORDレコード
- ord-da4794a09a0042efaeb2e246e4600411
- 出典データセット
- uspto-grants-2007_02
- 特許番号
- US07173153B2
関連ノート
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