戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1647800作成日:2026年10月25日

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

https://huagongshe.com/reaction/1647800

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物1-(t-Butoxycarbonyl)-4-(5-methoxy-4-pyrimidinyl)-3-methylpiperazineHCID 19921661—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物1-(5-Methoxy-4-pyrimidinyl)-2-methylpiperazineHCID 1908147492%

反応手順

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 (pHS) 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) δ 8.32 (S, 1H), 7.87 (s, 1H), 4.83-4.68 (m, 1H), 4.26-4.19 (m, 1H), 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) .

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05434154
出典データセットuspto-grants-1995_07
ORD IDord-f9815f3289a34a398f3fa53c32ea02e3
出典メモuspto-grants-1995_07