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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38791생성일: 2026년 10월 25일

tert-Butanol → Tert-butyl{2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}carbamate

https://huagongshe.com/reaction/38791

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물TriethylamineHCID 8471—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물Sodium BicarbonateHCID 516892—
반응물2-(3-Chlorophenylamino)-4-trifluoromethylpyrimidine-5-carboxylic acidHCID 16719655—
생성물Tert-butyl{2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}carbamateHCID 68404320—

반응 조건

온도90 °C

반응 단계

To a mixture of 2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidine-5-carboxylic acid (307 mg), triethylamine (162 μL), and tert-butyl alcohol (9 mL) was added diphenylphosphorylazide (250 μL), followed by stirring at 90° C. for 7 hours. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution (50 mL), followed by extraction with ethyl acetate (50 mL), and then the extract was washed with saturated brine (30 mL). The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain tert-butyl {2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}carbamate (270 mg) as a pale yellow powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524727B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-cc9395f6678a4328bd0405ccf8eb2dbe
출처 메모uspto-grants-2013_09