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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 235843생성일: 2026년 10월 26일

Acetonitrile → N-(7-methoxy-1,8-naphthyridin-2-yl)-4-ethoxybenzamide

https://huagongshe.com/reaction/235843

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물4-Ethoxybenzoic acidHCID 12093—
반응물7-methoxy-1,8-Naphthyridin-2-amineHCID 21793027—
용매WaterHCID 962—
생성물N-(7-methoxy-1,8-naphthyridin-2-yl)-4-ethoxybenzamideHCID 2021755467.7%

반응 조건

온도4 °C

반응 단계

The procedure is similar to that described in Example 1, but starting with 4-ethoxybenzoic acid (8 g), N,N'-carbonyldiimidazole (7.8 g) and 2-amino-7-methoxy-1,8-naphthyridine (5.6 g). The product produced by precipitation in water (9.4 g; m.p. 74° C.) is dissolved in boiling acetonitrile (94 cc). After 3 hours' cooling at 4° C., the crystallised solid is separated by filtration, washed with acetonitrile (3×20 cc) and dried at 30° C. under reduced pressure (0.067 kPa). N-(7-methoxy-1,8-naphthyridin-2-yl)-4-ethoxybenzamide (7 g) is produced, m.p. 145° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04642308
출처 데이터셋uspto-grants-1987_02
ORD IDord-5cc7a14a75ef4fc98a49b3b98d004259
출처 메모uspto-grants-1987_02