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HRID 464828생성일: 2026년 10월 25일

Potassium Iodide → benzyl 3(S)-tert-butoxycarbonylamino-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine-5-acetate

https://huagongshe.com/reaction/464828

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Acetic acid, 2-chloro-, phenylmethyl esterHCID 8786—
반응물Potassium CarbonateHCID 11430—
반응물(S)-tert-Butyl (4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)carbamateHCID 18599719—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물benzyl 3(S)-tert-butoxycarbonylamino-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine-5-acetateHCID 1859973462.1%

반응 단계

In 150 ml of N,N-dimethylformamide is dissolved 12.3 g of 3(S)-tert-butoxycarbonylamino-2,3,4,5-tetrahydro-1,5-benzoxazepine-4-one, and 8.7 g of benzyl chloroacetate, 8.7 g of anhydrous potassium carbonate and 1 g of potassium iodide are added to the solution. After stirring for 15 hours, the mixture is poured in ice-cooled water. The deposited material is collected by filtration, washed with water and recrystallized from ethyl acetate-hexane to give 11.7 g of benzyl 3(S)-tert-butoxycarbonylamino-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine-5-acetate as colorless prisms, melting at 122°-124° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04548932
출처 데이터셋uspto-grants-1985_10
ORD IDord-c385b3b2796346a39fc74091c538b86d
출처 메모uspto-grants-1985_10