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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1032729생성일: 2026년 10월 26일

Hexamethylphosphoramide → Ethyl 1,4-dihydro-1-ethyl-7-(3-pyridinyl)4-oxo-3-quinolinecarboxylate

https://huagongshe.com/reaction/1032729

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylphosphoramideHCID 12679—
반응물3-(Trimethylstannyl)pyridineHCID 10868445—
반응물Ethyl 7-bromo-1-ethyl-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 14851995—
반응물Chloroform ethanolHCID 21889567—
촉매HCID 178418476HCID 178418476—
용매1,4-DioxaneHCID 31275—
생성물Ethyl 1,4-dihydro-1-ethyl-7-(3-pyridinyl)4-oxo-3-quinolinecarboxylateHCID 2179090756.3%

반응 단계

A suspension of 10.0 g ethyl 7-bromo-1,4-dihydro-1-ethyl-4-oxo-3-quinolinecarboxylate (U.S. Pat. No. 3,753,993), 0.64 g dichlorobis(triphenylphosphine)palladium, 10.9 g 3-trimethylstannylpyridine and 6.5 ml hexamethylphosphoramide in 40 ml dioxane was heated at reflux under nitrogen for 48 hrs. The reaction mixture was filtered through neutral alumina, eluted with chloroform, washed with water, and dried over potassium carbonate. The solid product obtained by concentration in vacuo was subjected to chromatography (MPLC; 10:1 CHCl3/EtOH) to give 5.6 g of ethyl 1,4-dihydro-1-ethyl-7-(3-pyridinyl)4-oxo-3-quinolinecarboxylate, which was hydrolyzed by refluxing with 150 ml 3N hydrochloric acid for 1.5 hrs. The product which separated (3.9 g) was dried to give 1,4-dihydro-1-ethyl-7-(3-pyridinyl)-4-oxo-3-quinolinecarboxylic acid, m.p. 268-269° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04959363
출처 데이터셋uspto-grants-1990_09
ORD IDord-79c42d546171496696d100287e0aafdc
출처 메모uspto-grants-1990_09