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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280376생성일: 2026년 10월 23일

Acetic Acid → 2,3-dihydro-3-oxo-5H-thiazolo[2,3-b]quinazoline-2-acetic acid methyl ester

https://huagongshe.com/ko/reaction/280376

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium borohydrideHCID 4311764—
반응물TelluriumHCID 6327182—
반응물(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acid methyl esterHCID 54051732—
용매EthanolHCID 702—
생성물2,3-dihydro-3-oxo-5H-thiazolo[2,3-b]quinazoline-2-acetic acid methyl esterHCID 1364907832.3%

반응 조건

온도-20 °C

반응 단계

A suspension of sodium borohydride (3.03 g, 0.08 mol) and 4.38 g (0.034 mol) tellurium powder in 135 ml anhydrous ethanol was heated under nitrogen atmosphere for 15 min. After cooling to -20° C., 8.08 ml glacial acetic acid in 33.65 ml anhydrous ethanol was added dropwise, and the mixture was stirred at that temperature for 5 min, followed by the addition of 3.50 g (0.013 mol) of (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acid methyl ester in 13.5 ml anhydrous ethanol. The reaction mixture was allowed to warm up to ambient temperature and stirred overnight. Then, the mixture was filtered through celite, and evaporated under reduced pressure. The residue was taken up in water and extracted with chloroform. The organic extract was dried over anhydrous magnesium sulfate and evaporated under reduced pressure, yielding 1.16 g of 2,3-dihydro-3-oxo-5H-thiazolo[2,3-b]quinazoline-2-acetic acid methyl ester. Mp 143°-144° C. after recrystallization from ethyl acetate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04588812
출처 데이터셋uspto-grants-1986_05
ORD IDord-f5731bc72c454b01b975e3e4261ed7dd
출처 메모uspto-grants-1986_05