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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 651597생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/651597

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PhenolHCID 996—
반응물Potassium HydroxideHCID 14797—
반응물7-Methoxy-naphthalene-2-sulfonic acid[1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(s)-yl]-amideHCID 15545831—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물7-Methoxynaphthalene-2-sulfonic acid [1-(1-phenoxy-isoquinolin-7-ylmethyl)-oxopyrrolidin-3-(r,s)-yl]-amideHCID 1208535783.3%

반응 조건

온도90 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06281227B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-e7f13aad33924752ab5db612310051c2
출처 메모uspto-grants-2001_08