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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 235805생성일: 2026년 10월 26일

Ethanol → N-(7Chloro-1,8-naphthyridin-2-yl)-1,4-cyclohexadiene-1-carboxamide

https://huagongshe.com/reaction/235805

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물7-Chloro-1,8-naphthyridin-2-amineHCID 85199—
반응물1,4-Cyclohexadiene-1-carboxylic acidHCID 297211—
용매WaterHCID 962—
생성물N-(7Chloro-1,8-naphthyridin-2-yl)-1,4-cyclohexadiene-1-carboxamideHCID 2021754333%

반응 조건

온도4 °C

반응 단계

The procedure is similar to that described in Example 1, but starting with 1,4-cyclohexadiene-1-carboxylic acid (6.2 g), N,N'-carbonyldiimidazole (8 g) and 2-amino-7-chloro-1,8-naphthyridine (8 g). The product produced by precipitation in water (11 g; m.p. 205° C.) is dissolved in boiling ethanol (250 cc). After 2 hours' cooling at 4° C., the crystallised solid is separated by filtration, washed with ethanol (3×15 cc) and dried at 40° C. under reduced pressure (0.067 kPa). N-(7Chloro-1,8-naphthyridin-2-yl)-1,4-cyclohexadiene-1-carboxamide (4.2 g) is produced, m.p. 210° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04642308
출처 데이터셋uspto-grants-1987_02
ORD IDord-67f63937ad5640b7979af9cf1aff7358
출처 메모uspto-grants-1987_02