Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1641453생성일: 2026년 10월 27일
Phosphorus oxybromide → pentyl 3-bromo-1-(3-chloro-2-pyridinyl)-4,5-dihydro-1H-pyrazole-5-carboxylate
https://huagongshe.com/reaction/1641453
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosphorus oxybromide | HCID 24613 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Pentyl 2-(3-chloro-2-pyridinyl)-5-oxopyrazolidine-3-carboxylate | HCID 59549450 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | pentyl 3-bromo-1-(3-chloro-2-pyridinyl)-4,5-dihydro-1H-pyrazole-5-carboxylate | HCID 59549455 | 137.5% |
반응 단계
A mixed solution comprising 1.2 g of pentyl 2-(3-chloropyridin-2-yl)-5-oxopyrazolidine-3-carboxylate, 0.59 g of phosphorus oxybromide and 18 ml of acetonitrile was gradually heated, and 25 minutes later, the mixed solution was refluxed with heating for one hour. After the reaction liquid was stood to cool, it was slowly added to a saturated sodium hydrogen carbonate aqueous solution, followed by stirring for 5 minutes. The mixed liquid was subjected to extraction with ethyl acetate, and the organic layer was washed with a sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1 to 8/2) to obtain 1.06 g of the desired product (melting point: 39 to 42° C.) in the form of pale yellow crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08115006B2 |
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| 출처 데이터셋 | uspto-grants-2012_02 |
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| ORD ID | ord-b47c9ea67e0f4747a6b5cd6689948e58 |
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| 출처 메모 | uspto-grants-2012_02 |
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