Hydrochloric Acid → (3-Methylpyrrolidin-3-yl)methanol hydrochloride
反応式
[OH:1][CH2:2][C:3]1([CH3:15])[CH2:7][CH2:6][N:5](C(OC(C)(C)C)=O)[CH2:4]1.CO.[ClH:18]>>[ClH:18].[CH3:15][C:3]1([CH2:2][OH:1])[CH2:7][CH2:6][NH:5][CH2:4]1参加物
4
実験手順
tert-butyl 3-(hydroxymethyl)-3-methylpyrrolidine-1-carboxylate (0.31 g, 1.44 mmol, see WO 2009132986) was dissolved in HCl in methanol (1.25M, 3.5 mL, 4.32 mmol). The reaction mixture was stirred at RT overnight and then the mixture was evaporated. Ethanol was added and the mixture was again evaporated to afford 243 mg. The crude product was used in the next step without further purification.
後処理
- customthe mixture was evaporated
- additionEthanol was added
- customthe mixture was again evaporated
- customto afford 243 mg
- customThe crude product was used in the next step without further purification
出典と根拠
- ORDレコード
- ord-6b9f9abe7b2e4461acffaa9c909ff603
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08546375B2
反応ノート
読み込み中…