関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2-Bromopropanedial | HCID 74945 | — |
| 反応物 | ethyl 3-amino-1H-pyrazole-4-carboxylate | HCID 81472 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6-Bromopyrazolo[1,5-a]pyrimidine-3-carboxylic acid | HCID 25220793 | 50.9% |
反応手順
A solution of ethyl 5-amino-1H-pyrazole-4-carboxylate (2 g, 12.89 mmol) and sodium hydroxide (19.34 mL, 38.7 mmol) (aqueous, 2M) in ethanol (30 mL) was heated at 80° C. overnight. The reaction mixture was concentrated in vacuo to give a crude mixture of carboxylate and sodium hydroxide. The crude mixture was dissolved in ethanol (4 mL) and acetic acid (14 mL, 245 mmol). Whilst stirring the mixture, bromomalonaldehyde (1.947 g, 12.90 mmol) was added and then the mixture heated to 70° C. for 1 h. The reaction mixture was allowed to cool and the precipitate was filtered and washed with ethanol. The solid product was dried in a vacuum oven to give the title compound (1.589 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08093249B2 |
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| 出典データセット | uspto-grants-2012_01 |
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| ORD ID | ord-5249bd5d12a84c86b40b10be0ee46e27 |
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| 出典メモ | uspto-grants-2012_01 |
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