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HRID 231512作成日:2026年10月27日
Triethylsilane → 4,5,6,7-Tetrahydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide
https://huagongshe.com/reaction/231512
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylsilane | HCID 12052 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 4,5-Dihydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide | HCID 2737093 | — |
| 溶媒 | Trifluoroacetic acid | HCID 6422 | — |
| 生成物 | 4,5,6,7-Tetrahydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide | HCID 135621397 | — |
反応手順
A solution of 3.44 g of 4,5-dihydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide (Ex. 24) in 40 ml of trifluoroacetic acid was stirred under nitrogen and heated to 60° C. in an oil bath. Then 5.0 ml of triethylsilane was added and the mixture was stirred at 60° C. for 24 hours. The reaction mixture was cooled and carefully poured into a beaker containing a 25% aqueous solution of potassium hydroxide and cracked ice. The product which precipitated was extracted into chloroform. The chloroform was washed with water, dried over anhydrous sodium sulfate and filtered. The filtrate was evaporated in vacuo and gave crystals which were recrystallized from toluene-hexane to give the desired product, mp 152°-154° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04847256 |
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| 出典データセット | uspto-grants-1989_07 |
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| ORD ID | ord-eec79a0350064775b60e18124d16bc30 |
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| 出典メモ | uspto-grants-1989_07 |
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