Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69115생성일: 2026년 10월 23일
N-methyl-2-pyrrolidone → N-{4-bromo-2-[1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-5-yl]-5-(trifluoromethyl)phenyl}-2,2,2-trifluoroacetamide
https://huagongshe.com/ko/reaction/69115
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Oxan-4-ylhydrazine dihydrochloride | HCID 50988431 | — |
| 반응물 | HCID 86694320 | HCID 86694320 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | N-{4-bromo-2-[1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-5-yl]-5-(trifluoromethyl)phenyl}-2,2,2-trifluoroacetamide | HCID 86694319 | 42.1% |
반응 단계
To a mixture of 6.0 g of tetrahydro-2H-pyran-4-ylhydrazine dihydrochloride and 175 mL of N-methylpyrrolidone was added 11 mL of DIPEA, followed by stirring at room temperature for 20 minutes. To the reaction mixture was added 8.86 g of N-{4-bromo-2-[(2E)-3-(dimethylamino)prop-2-enoyl]-5-(trifluoromethyl)phenyl}-2,2,2-trifluoroacetamide, followed by stirring at 110° C. for 1 hour. To the reaction mixture was added water, followed by extraction with isopropyl acetate, and the organic layer was washed with saturated brine. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (chloroform/methanol). The obtained oil was triturated with diethyl ether/n-hexane to obtain 4.19 g of N-{4-bromo-2-[1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-5-yl]-5-(trifluoromethyl)phenyl}-2,2,2-trifluoroacetamide.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822448B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-827bb13d420d45d79a6d08b3559fd55b |
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| 출처 메모 | uspto-grants-2014_09 |
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