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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50073생성일: 2026년 10월 24일

Potassium Carbonate → 3-[3-(4-Amino-4-phenylpiperid-1-yl)propyl]-1-benzoyl-3-(3,4-dichlorophenyl)-piperidine

https://huagongshe.com/ko/reaction/50073

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-[4-(pyrrolidin-1-ylcarbonyl)piperid-1-yl]propyl]piperidine hydrochlorideHCID 22741714—
반응물4-Amino-4-phenylpiperidine dibenzenesulfonateHCID 22741754—
용매acetonitrile N,N-dimethylformamideHCID 21891449—
생성물3-[3-(4-Amino-4-phenylpiperid-1-yl)propyl]-1-benzoyl-3-(3,4-dichlorophenyl)-piperidineHCID 1528559174.6%

반응 조건

온도100 °C

반응 단계

A mixture of 6.81 g of 4-amino-4-phenylpiperidine dibenzenesulfonate, 5.2 g of the compound obtained in step B of EXAMPLE 1 and 6.1 g of K2CO3 in 30 ml of a DMF/acetonitrile mixture (50/50; v/v) is heated at 100° C. for 5 hours. It is concentrated under vacuum, the residue is taken up with water and extracted with AcOEt, the organic phase is washed with water and with saturated NaCl solution and dried over MgSO4 and the solvent is evaporated off under vacuum. The residue is chromatographed on silica H using a DCM/MeOH mixture (from 99/1; v/v to 85/15; v/v) as the eluent to give 3.6 g of the expected product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710042B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-7452e02e40fe423e8265ad2b71445983
출처 메모uspto-grants-2004_03