Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2050508생성일: 2026년 10월 26일
Triethylsilane → 4,5,6,7-Tetrahydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide
https://huagongshe.com/reaction/2050508
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylsilane | HCID 12052 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 4,5-Dihydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide | HCID 2737093 | — |
| 용매 | Trifluoroacetic acid | HCID 6422 | — |
| 생성물 | 4,5,6,7-Tetrahydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide | HCID 135621397 | — |
반응 단계
A solution of 3.44 g of 4,5-dihydro-7-(3-trifluoromethyl)phenyl)pyrazolo(1,5-a)pyrimidine-3-carboxamide (Example 8) in 40 ml of trifluoroacetic acid is stirred under nitrogen and heated to 60° C. in an oil bath. Then 5.0 ml of triethylsilane is added and the mixture is stirred at 60° C. for 24 hours. The reaction mixture is cooled and carefully poured into a beaker containing a 25 percent aqueous solution of potassium hydroxide and cracked ice. The product which precipitates is extracted into chloroform, and the extract is washed with water, dried over anhydrous sodium sulfate and filtered. The filtrate is evaporated in vacuo to give crystals which are then recrystallized from toluene-hexane to give the desired product, mp 152-154° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05013737 |
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| 출처 데이터셋 | uspto-grants-1991_05 |
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| ORD ID | ord-e7de8176c5cc45b6b607074fc86f9053 |
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| 출처 메모 | uspto-grants-1991_05 |
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