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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428419생성일: 2026년 10월 25일

Water → 7-Chloro-3-[[(tert-butylamino)oxy]carbonyl]pyrazolo[3,4-c][1]benzazepine-4,10(1H,9H)-dione

https://huagongshe.com/reaction/428419

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물N-tert-butylhydroxylamine hydrochlorideHCID 2777896—
반응물HCID 178524941HCID 178524941—
용매DimethylformamideHCID 6228—
생성물7-Chloro-3-[[(tert-butylamino)oxy]carbonyl]pyrazolo[3,4-c][1]benzazepine-4,10(1H,9H)-dioneHCID 17844994761%

반응 단계

A solution of 7-chloro-3-(carboxy)pyrazolo[3,4-c][1]-benzazepine-4,10(1H,9H)-dione (400 mg, 1.37 mmol) (compound of Example 9) and 1,1′-carbonyldiimidazole (334 mg, 2.06 mmol) in N,N-dimethylformamide (16 mL) was stirred for 1 hour. In one portion, N-tert-butylhydroxylamine hydrochloride (516 mg, 4.11 mmol) was added and the solution was stirred for 17 hours at room temperature. To the resulting solution was added water (20 mL). The insoluble material was filtered and washed with hot methanol (3×20 mL) to give the title compound (300 mg, 61% yield, m.p. 258° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313290B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-51e08f90a2bb441ea101b0be1eafcb1e
출처 메모uspto-grants-2001_11