関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Difluoroacetic acid | HCID 9788 | — |
| 反応物 | 3-Chloro-6-hydrazinopyridazine | HCID 100787 | — |
| 生成物 | 6-Chloro-3-(difluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine | HCID 1472385 | 84.7% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08003649B2 |
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| 出典データセット | uspto-grants-2011_08 |
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| ORD ID | ord-0ceaf4b1da1f4d33957a3227a815b9d9 |
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| 出典メモ | uspto-grants-2011_08 |
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