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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 394025생성일: 2026년 10월 24일

Dimethylformamide → (2r)-1-{(2s,4s)-4-Acetoxy-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonyl-n-{((3r)-1-cyclohexylmethyl-3-piperidyl)methyl}pyrrolidine-2-carboxamide

https://huagongshe.com/ko/reaction/394025

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물(2R)-N-{((3R)-1-cyclohexylmethyl-3-piperidyl)methyl}-1-{(2S,4R)-4-(methylsulfonyloxy)-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonylpyrrolidine-2-carboxyamideHCID 131724629—
촉매Tetrabutylammonium AcetateHCID 82707—
용매Ethyl AcetateHCID 8857—
생성물(2r)-1-{(2s,4s)-4-Acetoxy-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonyl-n-{((3r)-1-cyclohexylmethyl-3-piperidyl)methyl}pyrrolidine-2-carboxamideHCID 12149972—

반응 단계

A solution of 40 mg of (2R)-N-{((3R)-1-cyclohexylmethyl-3-piperidyl)methyl}-1-{(2S,4R)-4-(methylsulfonyloxy)-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonylpyrrolidine-2-carboxyamide and 30 mg of tetrabutylammonium acetate in 1 ml of N,N-dimethylformamide was stirred at 85° C. for 15 hours under heating. The reaction liquid was diluted with ethyl acetate, successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified with a preparative thin-layer chromatography (Kieselgel™ 60F254, Art. 5744 (Merck), chloroform/methanol/28% aqueous ammonia=100/8/1), to provide 14 mg of the title compound as a colorless oily substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809108B1
출처 데이터셋uspto-grants-2004_10
ORD IDord-8ce7075e514b496193cfb7e61b49b8a1
출처 메모uspto-grants-2004_10