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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2225341생성일: 2026년 10월 25일

4-Chlorobenzoic Acid → 2-(4-Chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid

https://huagongshe.com/reaction/2225341

반응식

참여 물질

역할이름HCID투입량
반응물4-Chlorobenzoic AcidHCID 6318—
반응물TriethylamineHCID 8471—
반응물Diethyl chlorophosphateHCID 13139—
반응물2-Amino-3-(2-quinolon-3-yl)propionic acidHCID 13342097—
용매TetrahydrofuranHCID 8028—
생성물2-(4-Chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acidHCID 13342103—

반응 단계

1.2 Grams of 2-amino-3-(2-quinolon-3-yl)propionic acid and 0.8 ml of triethylamine were suspended in 10 ml of tetrahydrofuran, then under stirring condition at a room temperature, a solution containing 1.0 g of diethyl chlorophosphate in 10 ml of tetrahydrofuran was added dropwise thereto, and the reaction mixture was stirred at a room temperature for 3 hours. To this reaction mixture was added a solution containing 1.0 g of p-chlorobenzoic acid in 10 ml of tetrahydrofuran dropwise and the whole reaction mixture was further stirred at a room temperature for 10 hours. After completion of the reaction, the crystals precipitated were removed by filtration, the filtrate was concentrated and to the residue was poured a saturated sodium hydrogencarbonate aqueous solution, then extracted with chloroform. The organic layer was washed with water and a saturated sodium chloride aqueous solution and dried with sodium sulfare. The solvent was removed by distillation and the residue was recrystallized from ethanol-water to obtain 0.9 g of 2-(4-chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid in the form of white powder product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE034722
출처 데이터셋uspto-grants-1994_09
ORD IDord-99ec18de92e04031a18330f50956821a
출처 메모uspto-grants-1994_09