反応式
C(OC(=O)[NH:7][C@H:8]1[CH2:12][CH2:11][N:10]([CH2:13][C:14]2[CH:23]=[C:22]3[C:17]([CH:18]=[CH:19][N:20]=[C:21]3[Cl:24])=[CH:16][CH:15]=2)[C:9]1=[O:25])(C)(C)C.Cl>CCOC(C)=O>[ClH:24].[NH2:7][C@H:8]1[CH2:12][CH2:11][N:10]([CH2:13][C:14]2[CH:23]=[C:22]3[C:17]([CH:18]=[CH:19][N:20]=[C:21]3[Cl:24])=[CH:16][CH:15]=2)[C:9]1=[O:25]参加物
4
反応条件
- 温度
- 0 °C
実験手順
To a solution of [1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3(S)-yl]-carbamic acid tert-butyl ester (2.1 g, 5.6 mmol) in EtOAc (170 mL) at 0° C. is bubbled HCl gas for 5 minutes. The solution is stirred at 0° C. for 15 minutes, then the ice bath is removed and the solution allowed to warn to room temperature. After 4 hours at room temperature, the solution is concentrated and the remaining solid is washed with ether to give the title compound (1.74 g, 5.6 mmol) as a pale yellow solid.
後処理
- customthe ice bath is removed
- customto warn to room temperature
- waitAfter 4 hours at room temperature
- concentrationthe solution is concentrated
- washthe remaining solid is washed with ether
出典と根拠
- ORDレコード
- ord-d0b56a0b486644ca9bd4439b8b3becfc
- 出典データセット
- uspto-grants-2001_08
- 特許番号
- US06281227B1
関連ノート
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