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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8138생성일: 2026년 10월 23일

1-Phenylpiperazine → Methyl 4-{[(5-ethoxy-5-oxopentyl)(2-{[5-(4-phenylpiperazino)-pentyl]oxy}phenethyl)amino]methyl}benzoate

https://huagongshe.com/ko/reaction/8138

반응식

참여 물질

역할이름HCID투입량
반응물1-PhenylpiperazineHCID 7096—
반응물TriethylamineHCID 8471—
반응물Methyl 4-{[{2-[(5-bromopentyl)oxy]phenethyl}(5-ethoxy-5-oxopentyl)amino]methyl}benzoateHCID 22015034—
용매TetrahydrofuranHCID 8028—
생성물Methyl 4-{[(5-ethoxy-5-oxopentyl)(2-{[5-(4-phenylpiperazino)-pentyl]oxy}phenethyl)amino]methyl}benzoateHCID 22015022—

반응 단계

200.0 mg (0.355 mmol) of methyl 4-{[{2-[(5-bromopentyl)oxy]phenethyl}(5-ethoxy-5-oxopentyl)amino]methyl}benzoate from Ex. 107, 69.21 mg of N-phenylpiperazine and 71.95 mg (0.711 mmol) of triethylamine in 2 ml of tetrahydrofuran are heated at reflux for 18 hours. The reaction solution is washed with water, concentrated and chromatographed over silica gel using the mobile phase ethyl acetate/methanol 10/1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087644B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-e62791e523bc48a79da21cd90562ab8c
출처 메모uspto-grants-2006_08