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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 478628생성일: 2026년 10월 25일

Nitrogen → Methyl 4-(4-propan-2-yl-piperazin-1-yl)benzoate

https://huagongshe.com/reaction/478628

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물OxygenHCID 977—
반응물Potassium CarbonateHCID 11430—
반응물Methyl 4-bromobenzoateHCID 12081—
반응물1-IsopropylpiperazineHCID 78013—
반응물2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
용매1,2-DimethoxyethaneHCID 8071—
생성물Methyl 4-(4-propan-2-yl-piperazin-1-yl)benzoateHCID 69129778—

반응 단계

Tris-(dibenzylidene-acetone)-dipalladium (0.05 mmol), (2′-dicyclohexylphosphanyl-biphenyl-2-yl)-dimethyl-amine (0.1 mmol) and potassium carbonate (4.6 mmol) are suspended in 1,2-dimethoxyethane (10 ml) in an oxygen-free atmosphere (N2). 4-Bromo-benzoic acid methyl ester (3.3 mmol) and 1-isopropyl-piperazine (3.9 mmol) are added and the stirred mixture is heated under reflux for 28 hours. After cooling the solvent is evaporated and water is added to the residue, which is then extracted three times with ethyl acetate. The combined extract is dried over sodium sulfate and evaporated. The residue is purified by flash chromatography on silica gel with (CH2Cl2/MeOH=95:5) as mobile phase. The product containing fractions are combined and evaporated. The residue is suspended in diethylether/pentane and the solid filtered of and dried (vacuum). A pale-brown powder with Rf=0.23 (CH2Cl2/MeOH=95:5) is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06642239B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-9c327ad5f7cf4604b824c2e783901015
출처 메모uspto-grants-2003_11