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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1480생성일: 2026년 10월 24일

Triethylamine → 1-(5-Acetamido-2-chloro-4-fluorophenyl)-3-(2-propynyl)urea

https://huagongshe.com/ko/reaction/1480

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Phenyl chloroformateHCID 15891—
반응물PropargylamineHCID 239041—
반응물N-(5-amino-4-chloro-2-fluorophenyl)acetamideHCID 11769584—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-(5-Acetamido-2-chloro-4-fluorophenyl)-3-(2-propynyl)ureaHCID 53873711—

반응 단계

A solution of 5'-amino-4'-chloro-2'-fluoroacetanilide (11.25 g, 55.6 mmol), and triethylamine (7.70 mL, 55.6 mmol) in tetrahydrofuran is added dropwise to a stirred solution of phenylchloroformate (8.70 mL, 69.4 mmol) in tetrahydrofuran while maintaining the reaction mixture temperature at 25°-30° C. After the addition is complete, the reaction mixture is stirred at room temperature for 75 minutes, and poured into ethyl acetate. The organic mixture is washed sequentially with water, saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a tan solid. A solution of the solid in tetrahydrofuran is treated with propargylamine (9.52 mL, 139 mmol), refluxed for 1 hour, and poured into water. The aqueous mixture is filtered to obtain a solid which is washed sequentially with water, 0.5N hydrochloric acid and water, and dried overnight to give the title product as a beige solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726126
출처 데이터셋uspto-grants-1998_03
ORD IDord-5a556d937a384abda5eb0822445fcd79
출처 메모uspto-grants-1998_03