関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Azide | HCID 33557 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 6-Chloroimidazo[1,2-b]pyridazine-2-carbonyl chloride | HCID 57749429 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | Azido(6-chloroimidazo[1,2-b]pyridazin-2-yl)methanone | HCID 57749436 | — |
反応手順
To a solution of 6-chloroimidazo[1,2-b]pyridazine-2-carbonyl chloride from Step 1 (2.2 g, 10 mmol) in acetone (40 mL) was added sodium azide (0.43 g, 6.6 mmol, solution in 1.5 mL H2O). The mixture was stirred at 25° C. for 1 h then poured into aq. NaHCO3. The solid precipitate was collected by careful filtration. The filtercake was not allowed to go dry (solvent-free). The filtercake was washed with benzene (2×50 mL) and then transferred to a 150-mL, round-bottomed flask. To azeotropically remove residual water, the solid was suspended in benzene (75 mL) and then concentrated to one-third its volume. Then once again the material was suspended in benzene (75 mL) and concentrated to near dryness to provide the title compound, which was taken on to the next step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07820665B2 |
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| 出典データセット | uspto-grants-2010_10 |
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| ORD ID | ord-986a0a74087a4f8a961d4020fe3e4147 |
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| 出典メモ | uspto-grants-2010_10 |
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