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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251966생성일: 2026년 10월 25일

1,2-Dimethylhydrazine dihydrochloride → 4-bromo-N-[4-chloro-2-(N,N'-dimethylhydrazinocarbonyl)-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxamide

https://huagongshe.com/reaction/251966

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Dimethylhydrazine dihydrochlorideHCID 9380—
반응물Potassium CarbonateHCID 11430—
반응물2-[4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrol-2-yl]-6-chloro-8-methyl-4H-3,1-benzoxazine-4-oneHCID 66853831—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-bromo-N-[4-chloro-2-(N,N'-dimethylhydrazinocarbonyl)-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxamideHCID 5778018723.3%

반응 단계

To a mixture of 0.29 g of N,N′-dimethylhydrazine dihydrochloride, 1 ml of water, 0.31 g of potassium carbonate and 10 ml of N,N-dimethylformamide was added 1.0 g of 2-[4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrol-2-yl]-6-chloro-8-methyl-4H-3,1-benzoxazine-4-one. The resulting mixture was stirred at room temperature for 6 hours. Water was poured into the reaction mixture, and the mixture was extracted with ethyl acetate three times. The organic layers were combined, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel chromatography to obtain 0.26 g of 4-bromo-N-[4-chloro-2-(N,N′-dimethylhydrazinocarbonyl)-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxamide of the formula:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07867949B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-0ba5eadd7aba4b8dbbd57508763f68cd
출처 메모uspto-grants-2011_01