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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280373생성일: 2026년 10월 26일

Phenol → (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic Acid Phenyl Ester

https://huagongshe.com/reaction/280373

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물TriethylamineHCID 8471—
반응물Sodium BicarbonateHCID 516892—
반응물N,N-bis(2-oxo-3-oxazolidinyl)phosphorodiamidic chlorideHCID 21249497—
반응물(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acidHCID 54200705—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic Acid Phenyl EsterHCID 54508713—

반응 단계

A solution of 1.30 g (5 mmols) (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acid, 1.27 g (5 mmols) N,N-bis(2-oxo-3-oxazolidinyl)phosphorodiamidic chloride, 0.49 g (5.2 mmols) phenol, and 1.10 g (10 mmols) triethylamine, in 10 ml dichloromethane was stirred at room temperature, under nitrogen atmosphere for 18 hours. Then, 10 ml of water (made slightly basic with sodium bicarbonate) were added. The precipitate was filtered of and the filtrate was dried over anhydrous magnesium sulfate, and evaporated to dryness under reduced pressure. The residual orange-yellow solid was recrystallized from anhydrous ethanol. Yield--0.62 g. Mp 194°-195° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04588812
출처 데이터셋uspto-grants-1986_05
ORD IDord-9bc3fb30f72f49fa81b82afc6e70df78
출처 메모uspto-grants-1986_05