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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 651600생성일: 2026년 10월 25일

Methyl iodide → 7-Methoxynaphthalene-2-sulfonic acid [1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]-methylamide

https://huagongshe.com/reaction/651600

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물7-Methoxy-naphthalene-2-sulfonic acid[1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(s)-yl]-amideHCID 15545831—
용매AcetoneHCID 180—
용매DichloromethaneHCID 6344—
생성물7-Methoxynaphthalene-2-sulfonic acid [1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]-methylamideHCID 5715176359.2%

반응 단계

To a solution of 7-methoxynaphthalene-2-sulfonic acid [1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]-amide (0.151 g, 0.304 mmol) in acetone (20 mL) is added potassium carbonate (0.084 g, 0.608 mmol) followed by methyl iodide (0.12 mL, 1.93 mmol). The resulting mixture is heated to reflux overnight, then cooled to room temperature and diluted with methylene chloride. The solution is washed with saturated NaHCO3 solution, water and brine. The organic layer is dried over MgSO4, filtered and concentrated. The residue is purified by column chromatography eluting with 5% MeOH/CH2Cl2 to give the product (0.093 mg, 0.18 mmol) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06281227B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-f82e18e090d44227aee6525dd6c6293f
출처 메모uspto-grants-2001_08