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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50059생성일: 2026년 10월 25일

Water → 1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-(4-piperidinopiperid-1-yl)propyl]-piperidine dihydrochloride hemihydrate

https://huagongshe.com/reaction/50059

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물1,4'-BipiperidineHCID 78607—
반응물1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-[4-(pyrrolidin-1-ylcarbonyl)piperid-1-yl]propyl]piperidine hydrochlorideHCID 22741714—
용매Ethyl AcetateHCID 8857—
용매acetonitrile N,N-dimethylformamideHCID 21891449—
생성물1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-(4-piperidinopiperid-1-yl)propyl]-piperidine dihydrochloride hemihydrateHCID 131721652—

반응 조건

온도100 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710042B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-f5b4b110951240c1b5c5e985d48e12ea
출처 메모uspto-grants-2004_03