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HRID 651597作成日:2026年10月26日

Hydrochloric Acid → 7-Methoxynaphthalene-2-sulfonic acid [1-(1-phenoxy-isoquinolin-7-ylmethyl)-oxopyrrolidin-3-(r,s)-yl]-amide

https://huagongshe.com/reaction/651597

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物PhenolHCID 996—
反応物Potassium HydroxideHCID 14797—
反応物7-Methoxy-naphthalene-2-sulfonic acid[1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(s)-yl]-amideHCID 15545831—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物7-Methoxynaphthalene-2-sulfonic acid [1-(1-phenoxy-isoquinolin-7-ylmethyl)-oxopyrrolidin-3-(r,s)-yl]-amideHCID 1208535783.3%

反応条件

温度90 °C

反応手順

Phenol (6.81 g, 72.4 mmol) and potassium hydroxide ( 0.41 g, 7.31 mmol) are added to 7-methoxynaphthalene-2-sulfonic acid [1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]-amide (1.8 g, 3.6 mmol) and heated to 90° C. until a homogeneous mixture is obtained. The mixture is stirred overnight at 90° C., then cooled to room temperature and diluted with methylene chloride (100 mL) and water. The aqueous layer is neutralized to pH 7 using 1 N HCl, then the two layers are separated and the aqueous layer is extracted with additional methylene chloride. The combined organic layers are washed with brine, dried over MgSO4, filtered and concentrated. The residue is purified by column chromatography eluting with a gradient of 30% EtOAc/hexanes to 60% EtOAc/hexanes to give the product (1.66 g, 3 mmol) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06281227B1
出典データセットuspto-grants-2001_08
ORD IDord-e7f13aad33924752ab5db612310051c2
出典メモuspto-grants-2001_08