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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-[4-(pyrrolidin-1-ylcarbonyl)piperid-1-yl]propyl]piperidine hydrochloride | HCID 22741714 | — |
| 반응물 | 4-Amino-4-phenylpiperidine dibenzenesulfonate | HCID 22741754 | — |
| 용매 | acetonitrile N,N-dimethylformamide | HCID 21891449 | — |
| 생성물 | 3-[3-(4-Amino-4-phenylpiperid-1-yl)propyl]-1-benzoyl-3-(3,4-dichlorophenyl)-piperidine | HCID 15285591 | 74.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06710042B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-7452e02e40fe423e8265ad2b71445983 |
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| 출처 메모 | uspto-grants-2004_03 |
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