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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46377생성일: 2026년 10월 25일

Ammonia → 2-(1-Azetidin-3-yl-1H-pyrazol-5-yl)-4-(trifluoromethyl)phenol

https://huagongshe.com/reaction/46377

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Trifluoroacetic acidHCID 6422—
반응물p-tolylmethyl N-(pyrazine-2-carbonylamino)carbamateHCID 478568—
반응물tert-Butyl 3-[5-(5-trifluoromethyl-2-hydroxyphenyl)-1H-pyrazol-1-yl]azetidine-1-carboxylateHCID 136063628—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2-(1-Azetidin-3-yl-1H-pyrazol-5-yl)-4-(trifluoromethyl)phenolHCID 136063620—

반응 단계

Trifluoroacetic acid (4 mL) was added to a stirred solution of tert-butyl 3-{5-[2-hydroxy-5-(trifluoromethyl)phenyl]-1H-pyrazol-1-yl}azetidine-1-carboxylate, (Preparation 857, 375 mg, 0.001 mol) in dichloromethane (10 mL) under nitrogen and the solution was stirred for 3 hours. The pink solution was evaporated and the residue dissolved in methanol and then the solvents were removed in vacuo. This was repeated a further two times. The residue was then suspended in diethyl ether and the solvents removed in vacuo to give an off-white foam. The foam was dissolved in water and treated with aqueous ammonia solution (7.5 molar) until pH10 to give a white precipitate. The mixture was extracted with ethyl acetate (6×30 mL). The combined organic layers were washed with saturated aqueous sodium chloride solution (2×20 mL), dried over anhydrous sodium sulphate, filtered and the solvents removed in vacuo to give a solid. The solid was triturated with diethyl ether to give the title compound as a white solid (200 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541588B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a9ae77906c1249d28ba9cf2b0bc1850d
출처 메모uspto-grants-2013_09