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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280374생성일: 2026년 10월 24일

Benzylamine → N-Benzyl-(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetamide

https://huagongshe.com/ko/reaction/280374

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물TriethylamineHCID 8471—
반응물DiethylphosphorylcyanideHCID 13586794—
반응물(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acidHCID 54200705—
용매DimethylformamideHCID 6228—
용매Benzene ethyl acetateHCID 21583983—
생성물N-Benzyl-(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetamideHCID 54292886—

반응 조건

온도0 °C

반응 단계

To a stirred mixture of (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acid (10.5 g, 1.9 mmols) and benzylamine (0.23 g, 2.1 mmols) in 25 ml dimethylformamide at 0° C., was added diethylphosphoryl cyanide (0.28 g, 2.1 mmols) (in dimethylformamide solution), followed by triethylamine (0.41 g, 4.0 mmols). The reaction mixture was stirred for 4 hours at 0° C. and then, at room temperature overnight. The reaction mixture was diluted with benzene-ethyl acetate and washed sequentially with 5% hydrochloric acid, water, saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride. The organic solution was dried over anhydrous magnesium sulfate, and evaporated to dryness under reduced pressure to give N-Benzyl-(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetamide which was recrystallized from ethyl acetate. Yield--0.09 g. Mp 258°-259° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04588812
출처 데이터셋uspto-grants-1986_05
ORD IDord-cf5698ff7a884e97b278358b34d4f565
출처 메모uspto-grants-1986_05