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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 235847생성일: 2026년 10월 26일

Acetonitrile → N-(7-Phenoxy-1,8-naphthyridin-2-yl)-3-dimethylaminobenzamide

https://huagongshe.com/reaction/235847

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물3-(Dimethylamino)benzoic acidHCID 66837—
반응물2-Amino-7-phenoxy-1,8-naphthyridineHCID 13787373—
용매WaterHCID 962—
생성물N-(7-Phenoxy-1,8-naphthyridin-2-yl)-3-dimethylaminobenzamideHCID 2021754783.3%

반응 조건

온도4 °C

반응 단계

The procedure is similar to that described in Example 1, but starting with 3-dimethylaminobenzoic acid (23.1 g), N,N'-carbonyldiimidazole (22.7 g) and 2-amino-7-phenoxy-1,8-naphthyridine (23.7 g). The product produced by precipitation in water (44 g; m.p. approximately 90° C.) is dissolved in boiling acetonitrile (1000 cc). After 3 hours' cooling at 4° C., the crystallised solid is separated by filtration, washed with acetonitrile (3×50 cc) and dried at 40° C. under reduced pressure (0.067 kPa). N-(7-Phenoxy-1,8-naphthyridin-2-yl)-3-dimethylaminobenzamide (32 g) is produced (m.p. 120° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04642308
출처 데이터셋uspto-grants-1987_02
ORD IDord-10fe8bff54bd4a9784448665a62cc5e4
출처 메모uspto-grants-1987_02