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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1463348생성일: 2026년 10월 25일

Trifluoroacetic acid → 1-(5-Methoxy-4-pyrimidinyl)-2-methylpiperazine

https://huagongshe.com/reaction/1463348

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물1-(t-Butoxycarbonyl)-4-(5-methoxy-4-pyrimidinyl)-3-methylpiperazineHCID 19921661—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물1-(5-Methoxy-4-pyrimidinyl)-2-methylpiperazineHCID 1908147492%

반응 단계

A solution of 1-(t-butoxycarbonyl)-4-(5-methoxy-4-pyrimidinyl)-3-methylpiperazine (1.70 g, 4.2 mmol) and trifluoroacetic acid (5 mL) in 50 mL of CH2Cl2 was stirred at r.t. under Ar for 18 h. The solution was evaporated, the residue was taken up in water and the mixture was basified (pH8) with 15% aqueous NaOH. The resulting (pH 8) mixture was extracted with ethyl acetate and the organic phase was washed (H2O, brine), dried (Na2SO4) and evaporated to give a semi-solid. This material was taken up in ether, filtered to remove insoluble material and the solution was evaporated to give the product (0.80 g, 92%) as an oil. It was used without further purification: IR (neat) 3300, 1580, 1540 cm-1 ; 1H nmr (200 MHz, CDCl3) δ8.32 (s, 1H), 7.87 (s, 1H), 4.83-4.68 (m, 1H), 4.26-4.19 (m, 1 H), 3.85 (s, 3H), 3.26-3.17 (m, 1H), 3.12-3.01 (m, 2H), 2.94-2.80 (m, 2H), 1.29 (d, J=6.8 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05300506
출처 데이터셋uspto-grants-1994_04
ORD IDord-273554b6dac043cc8d0508eda694d477
출처 메모uspto-grants-1994_04