Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252004생성일: 2026년 10월 24일
Tetrahydrofuran → 4-bromo-N-[4,6-dibromo-2-(N,N'-dimethylhydrazinocarbonyl)phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxamide
https://huagongshe.com/ko/reaction/252004
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 1,2-Dimethylhydrazine dihydrochloride | HCID 9380 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 6,8-dibromo-2-[4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrol-2-yl]-4H-3,1-benzoxazine-4-one | HCID 66854197 | — |
| 촉매 | Water | HCID 962 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-bromo-N-[4,6-dibromo-2-(N,N'-dimethylhydrazinocarbonyl)phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxamide | HCID 57780330 | 79.6% |
반응 단계
To a mixture of 0.42 g of N,N′-dimethylhydrazine dihydrochloride, five drops of water, 0.87 g of potassium carbonate and 10 ml of tetrahydrofuran was added 0.59 g of 6,8-dibromo-2-[4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrol-2-yl]-4H-3,1-benzoxazine-4-one. The resulting mixture was stirred at room temperature for 2 hours. Water was poured into the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel chromatography to obtain 0.52 g of 4-bromo-N-[4,6-dibromo-2-(N,N′-dimethylhydrazinocarbonyl)phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxamide of the formula:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07867949B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-bda843301c224fc7b8683dd5bb097550 |
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| 출처 메모 | uspto-grants-2011_01 |
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