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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

반응식

참여 물질

역할이름HCID투입량
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물DiisopropylethylamineHCID 81531—
반응물Oxan-4-ylhydrazine dihydrochlorideHCID 50988431—
반응물HCID 86694320HCID 86694320—
용매WaterHCID 962—
생성물N-{4-bromo-2-[1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-5-yl]-5-(trifluoromethyl)phenyl}-2,2,2-trifluoroacetamideHCID 8669431942.1%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822448B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-827bb13d420d45d79a6d08b3559fd55b
출처 메모uspto-grants-2014_09