돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 499184생성일: 2026년 10월 26일

Pyridine → 2,2,2-Trichloroethyl (3-tert-butyl-1-methyl-1H-pyrazol-5-yl)carbamate

https://huagongshe.com/reaction/499184

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Ethyl AcetateHCID 8857—
반응물2,2,2-Trichloroethyl chloroformateHCID 87063—
반응물3-tert-Butyl-1-methyl-1H-pyrazol-5-amineHCID 2735287—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2,2,2-Trichloroethyl (3-tert-butyl-1-methyl-1H-pyrazol-5-yl)carbamateHCID 59420872—

반응 조건

온도0 °C

반응 단계

To an ice-cooled solution of 5-tert-butyl-2-methyl-2H-pyrazol-3-ylamine (0.50 g, 3.26 mmol) and pyridine (0.27 mL, 3.29 mmol) in THF (THF, 10 mL) is added 2,2,2-trichloroethyl chloroformate (0.44 mL, 3.29 mmol). The reaction mixture is stirred at 0° C. for 30 min and then warmed to room temperature for 2 hours. Then the reaction mixture is distributed between ethyl acetate (100 mL) and water (100 mL). The aqueous phase is extracted with ethyl acetate (50 mL). The combined organic phases are washed with saturated NaCl (2×50 mL) and dried over anhydrous magnesium sulfate. After removal of solvent, the residue is purified on a silica gel chromatography by washing with ethyl acetate to provide a white solid (0.83 g, 78%, ES+(m/z) 329.9 [M+H]).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07767674B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-8ad732784b564b859fc67bd23cbc8055
출처 메모uspto-grants-2010_08