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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 962481생성일: 2026년 10월 26일

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → (+)-4-Phenyl4-[(1-(3,5-bis(trifluoromethyl)phenyl)-2-hydroxyethoxy)methyl]-1-(2-(pyrrolidinyl)acetamido)piperidine Hydrochloride

https://huagongshe.com/reaction/962481

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-(Pyrrolidin-1-yl)acetic acid hydrochlorideHCID 13022016—
반응물4-Phenyl-4-((1-(3,5-bis(trifluoromethyl)phenyl)-2-hydroxyethoxy) methyl)piperidine HydrochlorideHCID 19084700—
반응물HCID 178526977HCID 178526977—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물(+)-4-Phenyl4-[(1-(3,5-bis(trifluoromethyl)phenyl)-2-hydroxyethoxy)methyl]-1-(2-(pyrrolidinyl)acetamido)piperidine HydrochlorideHCID 19084703—

반응 단계

1-[3-Dimethylaminopropyl]-3-ethylcarbodiimide hydrochloride (797 mg), hydroxybenzo-triazole trihydrate (475 mg) and triethylamine (0.890 ml) were added to a stirred solution of 2-pyrrolidinyl acetic acid hydrochloride (528 mg) in dry dimethylformamide at room temperature. After 30 minutes a solution of the compound of Example 14 (800 mg) in dry dimethylformamide was added, followed by triethylamine (0.590 ml). The resulting solution was stirred at room temperature for 4 hours. The reaction was quenched with water and extracted into diethyl ether then the organic solution was dried (MgSO4) and evaporated to give a yellow oil. The residue was purified by chromatography on grade 3 neutral alumina (1% methanol/dichloromethane) then treated with ethereal hydrogen chloride to afford the title compound, mp=106°-108° C.;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05760018
출처 데이터셋uspto-grants-1998_06
ORD IDord-5faa7a865d2c4324a338648b88c1030b
출처 메모uspto-grants-1998_06