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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 580478생성일: 2026년 10월 26일

Pyridine → N-(7-methoxy-1,8-naphthyridin2-yl)-3-acetoxybenzamide

https://huagongshe.com/reaction/580478

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물3-(Chlorocarbonyl)phenyl acetateHCID 12998558—
반응물7-methoxy-1,8-Naphthyridin-2-amineHCID 21793027—
용매WaterHCID 962—
생성물N-(7-methoxy-1,8-naphthyridin2-yl)-3-acetoxybenzamideHCID 1398339578.6%

반응 단계

The procedure is similar to that described in Example 3, but starting with 2-amino-7-methoxynaphthyridine (3.5 g), 3-acetoxybenzoyl chloride (4.4 g) and anhydrous pyridine (40 cc). The reaction mixture is poured into water (400 cc) and the precipitate obtained is separated by filtration and then washed with water (6×100 cc) and dried in the air. On recrystallization from ethanol (140 cc) of the product thereby obtained, N-(7-methoxy-1,8-naphthyridin2-yl)-3-acetoxybenzamide (5.3 g), m.p. 172° C., is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04753941
출처 데이터셋uspto-grants-1988_06
ORD IDord-2e02604d1e1447bfb7a6e3d9f54c6d2c
출처 메모uspto-grants-1988_06