돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272089생성일: 2026년 10월 25일

Methyl bromide acetonitrile → (3S)-3-({({(2R)-1-({(2S,4R)-4-hydroxy-1-(3,3,3-triphenylpropanoyl)-2-pyrrolidinyl}carbonyl)-2-pyrrolidinyl}carbonyl)amino}methyl)-1,1-dimethylpiperidinium bromide

https://huagongshe.com/reaction/272089

반응식

참여 물질

역할이름HCID투입량
반응물Methyl bromide acetonitrileHCID 22594519—
반응물(2R)-1-{(2S,4R)-4-hydroxy-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonyl-N-{((3S)-1-methyl-3-piperidyl)methyl}pyrrolidine-2-carboxamideHCID 69100833—
생성물(3S)-3-({({(2R)-1-({(2S,4R)-4-hydroxy-1-(3,3,3-triphenylpropanoyl)-2-pyrrolidinyl}carbonyl)-2-pyrrolidinyl}carbonyl)amino}methyl)-1,1-dimethylpiperidinium bromideHCID 69101449—

반응 단계

To 15 mg of (2R)-1-{(2S,4R)-4-hydroxy-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonyl-N-{((3S)-1-methyl-3-piperidyl)methyl}pyrrolidine-2-carboxamide, 0.5 ml of 10% methyl bromide-acetonitrile was added at room temperature, followed by 12 hours' stirring. The solvent in the reaction liquid was distilled off under reduced pressure, and the resulting residue was purified by preparative thin-layer chromatography (aluminium oxide 60F254, Art. 5713 (Merck), choroform/methanol=18/1) to provide 15 mg of the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452908B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-654423ce16344b95b39d50fcd0af939a
출처 메모uspto-grants-2008_11