참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Difluoroacetic acid | HCID 9788 | — |
| 반응물 | 3-Chloro-6-hydrazinopyridazine | HCID 100787 | — |
| 생성물 | 6-Chloro-3-(difluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine | HCID 1472385 | 84.7% |
반응 단계
A mixture of 3-chloropyridazin-6-yl hydrazine (5.0 g, 34.72 mmol) and difluoroacetic acid (21.93 mL; ca. 347 mmol) was heated at 100° C. for 3 hours and then evaporated to dryness. The involatile residue was dissolved in ethyl acetate (200 mL) and washed sequentially with saturated aqueous sodium carbonate and then saturated brine. The organic phase was dried over MgSO4, filtered, and evaporated to give 6-chloro-3-difluoromethyl-[1,2,4]-triazolo[4,3-b]pyridazine (6.0 g, 84.7%) as a white solid that was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08003649B2 |
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| 출처 데이터셋 | uspto-grants-2011_08 |
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| ORD ID | ord-0ceaf4b1da1f4d33957a3227a815b9d9 |
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| 출처 메모 | uspto-grants-2011_08 |
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