Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 231512생성일: 2026년 10월 27일
Triethylsilane → 4,5,6,7-Tetrahydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide
https://huagongshe.com/reaction/231512
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 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 (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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04847256 |
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| 출처 데이터셋 | uspto-grants-1989_07 |
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| ORD ID | ord-eec79a0350064775b60e18124d16bc30 |
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| 출처 메모 | uspto-grants-1989_07 |
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