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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1582967생성일: 2026년 10월 26일

Dimethylformamide → N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylchloroacetamide

https://huagongshe.com/reaction/1582967

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Chloroacetyl chlorideHCID 6577—
반응물3-(3-Chlorobenzoyl)-2-ethylamino-6-methylpyridineHCID 11054902—
용매PyridineHCID 1049—
생성물N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylchloroacetamideHCID 22716666—

반응 단계

To a DMF solution of 3-(3-chlorobenzoyl)-2-ethylamino-6-methylpyridine were added chloroacetyl chloride and pyridine, followed by reaction at room temperature. Thereafter, the whole was worked up and purified in a usual manner to obtain N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]—N-ethylchloroacetamide. To an acetonitrile solution of the compound were added N-tert-butoxycarbonylpiperazine and potassium carbonate, followed by reaction under heating. Thereafter, the reaction mixture was worked up and purified in a usual manner to obtain 2-[4-tert-butoxycarbonylpiperazin-1-yl]—N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylacetamide. The resulting compound was reacted with sodium methoxide in methanol under heating. Thereafter, the reaction mixture was worked up and purified in a usual manner to obtain 3-(1 -tert-butoxycarbonylpiperazin-4-yl)-4-(3-chlorophenyl)-1-ethyl-7-methyl-1,8-naphthyridin-2(1H)-one. NMR1: 4.73 (2H, q, J=7.3 Hz), 3.15-3.35 (2H, m), 1.38 (9H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06740662B1
출처 데이터셋uspto-grants-2004_05
ORD IDord-2b7066718f6d4a3d956f6504ca1831b0
출처 메모uspto-grants-2004_05