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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 235844생성일: 2026년 10월 26일

4-Butoxybenzoic acid → N-(7-chloro-1,8-naphthyridin-2-yl)-4-butoxybenzamide

https://huagongshe.com/reaction/235844

반응식

참여 물질

역할이름HCID투입량
반응물4-Butoxybenzoic acidHCID 72971—
반응물7-Chloro-1,8-naphthyridin-2-amineHCID 85199—
용매WaterHCID 962—
생성물N-(7-chloro-1,8-naphthyridin-2-yl)-4-butoxybenzamideHCID 1357940935.2%

반응 단계

The procedure is similar to that described in Example 1, but starting with 4-butoxybenzoic acid (15.5 g), N,N'-carbonyldiimidazole (12.9 g) and 2-amino-7-chloro-1,8-naphthyridine (8.9 g). The product produced by precipitation in water (approximately 18 g; m.p. 140° C.) is purified by chromatography on a column 40 mm in diameter charged with silica (200 g; 0.063-0.2 mm), using methylene chloride as eluant and collecting 60-cc fractions. After concentration to dryness of fractions 8 to 12 at 40° C. under reduced pressure (4 kPa), N-(7-chloro-1,8-naphthyridin-2-yl)-4-butoxybenzamide (6.2 g) is produced, m.p. 197° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04642308
출처 데이터셋uspto-grants-1987_02
ORD IDord-2336dddbad3b4ae1a27ccf18b239c58f
출처 메모uspto-grants-1987_02