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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251960생성일: 2026년 10월 26일

1,2-Dimethylhydrazine dihydrochloride → 3-bromo-N-[4-chloro-2-(N,N'-dimethylhydrazinocarbonyl)-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/251960

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Dimethylhydrazine dihydrochlorideHCID 9380—
반응물Potassium CarbonateHCID 11430—
반응물2-(3-Bromo-1-(3-chloropyridin-2-yl)-1H-pyrazol-5-yl)-6-chloro-8-methyl-4H-benzo[d][1,3]oxazin-4-oneHCID 10253307—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물3-bromo-N-[4-chloro-2-(N,N'-dimethylhydrazinocarbonyl)-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamideHCID 57780299134.3%

반응 단계

To a mixture of 0.13 g of N,N′-dimethylhydrazine dihydrochloride, 1 ml of water, 0.14 g of potassium carbonate and 10 ml of tetrahydrofuran was added 0.23 g of 2-[3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazol-5-yl]-6-chloro-8-methyl-4H-3,1-benzoxazine-4-one, and the resulting mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into 30 ml of water, 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 residue was washed with ethyl acetate to obtain 0.35 g of 3-bromo-N-[4-chloro-2-(N,N′-dimethylhydrazinocarbonyl)-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide of the formula:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07867949B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-23130c76e306431eb6716c9a5dee7fe9
출처 메모uspto-grants-2011_01