Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 377801생성일: 2026년 10월 25일
Water → 1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-(4-piperidinopiperid-1-yl)propyl]-piperidine dihydrochloride hemihydrate
https://huagongshe.com/reaction/377801
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1,4'-Bipiperidine | HCID 78607 | — |
| 반응물 | 1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-(methanesulfonyloxy)propyl]piperidine | HCID 11812710 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | acetonitrile N,N-dimethylformamide | HCID 21891449 | — |
| 생성물 | 1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-(4-piperidinopiperid-1-yl)propyl]-piperidine dihydrochloride hemihydrate | HCID 131721652 | — |
반응 단계
A mixture of 0.55 g of 4-piperidinopiperidine, 1.3 g of the compound obtained in step B of EXAMPLE 1 and 1.14 g of K2CO3 in 10 ml of a DMF/acetonitrile mixture (50/50; v/v) is heated at 100° C. for 3 hours. The reaction mixture is poured into water and extracted with AcOEt, the organic phase is washed twice 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 DCM and then a DCM/MeOH mixture (98/2; v/v) as the eluent. The product obtained is dissolved in AcOEt, a stream of HCl gas is bubbled into the solution until the pH is 1, and ether is added until precipitation occurs. This gives 0.53 g of the expected product after filtration and drying, m.p.=265° C. (dec.).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06028082 |
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| 출처 데이터셋 | uspto-grants-2000_02 |
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| ORD ID | ord-37cac7d3991e4e97973640808ad711d8 |
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| 출처 메모 | uspto-grants-2000_02 |
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