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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5744생성일: 2026년 10월 23일

4-Hydroxybenzaldehyde → N-{2-[4-Chloro-N-(4-hydroxybenzyl) cinnamylamino]ethyl}-5-isoquinolinesulfonamide

https://huagongshe.com/ko/reaction/5744

반응식

참여 물질

역할이름HCID투입량
반응물4-HydroxybenzaldehydeHCID 126—
반응물N-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamideHCID 176156—
반응물Sodium cyanoborohydrideHCID 5003444—
촉매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물N-{2-[4-Chloro-N-(4-hydroxybenzyl) cinnamylamino]ethyl}-5-isoquinolinesulfonamideHCID 5364218959.3%

반응 단계

0.2 g of the product of Example 172 and 0.13 g of p-hydroxybenzaldehyde were dissolved in 10 ml of methanol, to the solution were added 60 mg of sodium cyanoborohydride and two drops of acetic acid, and the mixture was stirred for 2 days at a room temperature. The reaction mixture was concentrated under a reduced pressure, and after adding a saturated sodium chloride aqueous solution, extracted three times with 20 ml of ethyl acetate. The extracts were combined, washed with sodium chloride, dried over magnesium sulfate, filtered and concentrated under a reduced pressure. The resulting residue was purified on a silica gel column (silica gel 10 g, eluant: 2% methanol in chloroform), to obtain 150 mg of the title compound in a colorless amorphous form.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245034
출처 데이터셋uspto-grants-1993_09
ORD IDord-ad93cea3c46c4c05874b445fc5c954fd
출처 메모uspto-grants-1993_09