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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1582956생성일: 2026년 10월 26일

Sodium hydride → ethyl 4-{N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylcarbamoyl}butanoate

https://huagongshe.com/reaction/1582956

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-(3-Chlorobenzoyl)-2-ethylamino-6-methylpyridineHCID 11054902—
반응물Monoethyl chloroglutarateHCID 22716689—
용매DimethylformamideHCID 6228—
생성물ethyl 4-{N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylcarbamoyl}butanoateHCID 22716702—

반응 단계

A DMF solution of 3-(3-chlorobenzoyl)-2-ethylamino-6-methylpyridine was treated with 60% sodium hydride and then reacted with monoethyl chloroglutarate under heating. Thereafter, the whole was worked up and purified in a usual manner to obtain ethyl 4-{N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylcarbamoyl}butanoate. The resulting compound was reacted with sodium methoxide in ethanol under heating, then concentrated sulfuric acid was added to the reaction mixture, followed by reaction under heating for 2 days. Thereafter, the reaction mixture was worked up and purified in a usual manner to obtain ethyl 3-[4-(3-chlorophenyl)-1-ethyl-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]propanoate. MS: 399.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06740662B1
출처 데이터셋uspto-grants-2004_05
ORD IDord-275262b710cf4a448b90a8a6fff1385a
출처 메모uspto-grants-2004_05