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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1843생성일: 2026년 10월 23일

Phenylacetic Acid → 4-Acetamido-4-phenyl-1-[2-[1-(3,4-dichlorophenyl)-2-(N-methyl-N-benzylcarbonylamino)ethoxy]ethyl]piperidine hydrochloride hemihydrate

https://huagongshe.com/ko/reaction/1843

반응식

참여 물질

역할이름HCID투입량
반응물Phenylacetic AcidHCID 999—
반응물ChloroethaneHCID 6337—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물4-Acetamido-4-phenyl-1-[2-[1-(3,4-dichlorophenyl)-2-(N-methylamino)ethoxy]ethyl]piperidine dihydrochlorideHCID 19692500—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물4-Acetamido-4-phenyl-1-[2-[1-(3,4-dichlorophenyl)-2-(N-methyl-N-benzylcarbonylamino)ethoxy]ethyl]piperidine hydrochloride hemihydrateHCID 131720562—

반응 단계

0.46 ml of triethylamine and then 0.5 g of BOP are added to a mixture of 0.5 g of the compound obtained in EXAMPLE 11, step B), 0.127 g of phenylacetic acid and 10 ml of DCM. The resulting mixture is concentrated under vacuum and the residue is taken up with AcOEt, washed with water, with 1N NaOH solution and with saturated NaCl solution, dried over MgSO4 and concentrated under vacuum. The residue is chromatographed on silica gel H using DCM and then a DCM/MeOH mixture (94/6; v/v) as the eluent. The product obtained is taken up with DCM, acidified to pH 1 by the addition of hydrochloric ether and concentrated under vacuum to give 0.42 g of the expected hydrochloride after crystallization from iso ether. M.p.=125° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726313
출처 데이터셋uspto-grants-1998_03
ORD IDord-b505007df247456aa881670aca334437
출처 메모uspto-grants-1998_03