Sodium Hydroxide → 1-(6-Chloropyrimidin-4-yl)azetidin-3-ol
反応式
Cl[C:2]1[N:7]=[C:6]([Cl:8])[CH:5]=[CH:4][N:3]=1.Cl.[OH:10][CH:11]1[CH2:14][NH:13][CH2:12]1.[OH-].[Na+]>O>[Cl:8][C:6]1[N:7]=[CH:2][N:3]=[C:4]([N:13]2[CH2:14][CH:11]([OH:10])[CH2:12]2)[CH:5]=1参加物
5
実験手順
7.2 g (48.7 mmol) 2,4-dichloropyrimidine are initially introduced into 140 ml water. 5.3 g (48.7 mmol) 3-hydroxyazetidine hydrochloride and 48.7 ml 1 N sodium hydroxide solution are added and the mixture is heated at 90° C. for 72 h (the 2,4-dichloropyrimidine being detectably volatile and precipitating in crystalline form on the condenser). The solvent is removed in vacuo and the residue is dried to give 10.4 g of the crude product, which is reacted without further purification.
後処理
- customprecipitating in crystalline form on the condenser)
- customThe solvent is removed in vacuo
- customthe residue is dried
出典と根拠
- ORDレコード
- ord-5b075ba59a9b4b8082cb1b5a68c371b8
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08987261B2
反応ノート
読み込み中…