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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5732생성일: 2026년 10월 24일

Hydrochloric Acid → N-{1-(p-methoxybenzyl)-2-(4-oxopiperidino)ethyl}-N-methyl-5-isoquinolinesulfonamide

https://huagongshe.com/ko/reaction/5732

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물tetrahydrofuran N,N-dimethylformamideHCID 21974620—
반응물N-{2-(4,4-ethylenedioxypiperidino)-1-[p-(5-isoquinolinesulfonyloxy)benzyl]ethyl}-N-methyl-5-isoquinolinesulfonamideHCID 53669357—
생성물N-{1-(p-methoxybenzyl)-2-(4-oxopiperidino)ethyl}-N-methyl-5-isoquinolinesulfonamideHCID 19796293—

반응 단계

The amorphous compound obtained in Example 94 was subjected to alkaline hydrolysis, methylation with methyl iodide and potassium carbonate in dimethylformamide/tetrahydrofuran (1:1), and reflux with 3N hydrochloric acid, to obtain N-{1-(p-methoxybenzyl)-2-(4-oxopiperidino)ethyl}-N-methyl-5-isoquinolinesulfonamide in a colorless amorphous form.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245034
출처 데이터셋uspto-grants-1993_09
ORD IDord-941e293f0a7c46e8b8635a04d61fecdf
출처 메모uspto-grants-1993_09