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)CCCC>[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 51.4 g free sertraline base in 100 ml of n-pentanol was added dropwise over a period of about 30 minutes at room temperature onto 100 ml of n-pentanol containing 13 ml of 37% aqueous hydrochloric acid. About ¾ of the way through 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. 50 g of sertraline hydrochloride form II are obtained in a yield of 87%.
後処理
- additionAbout ¾ of the way through 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-3c146539305e4fbeb7ff469f3f6d136c
- 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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