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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22065생성일: 2026년 10월 23일

Dextroamphetamine → (R)-2-[(1-Phenylpropyl)amino]adenosine

https://huagongshe.com/ko/reaction/22065

반응식

참여 물질

역할이름HCID투입량
반응물DextroamphetamineHCID 5826—
반응물(R)-1-PhenylpropylamineHCID 5324978—
반응물(1S)-1-phenylpropan-1-amineHCID 6993773—
반응물(S)-2-[(phenylisopropyl)amino]adenosineHCID 67681966—
생성물(R)-2-[(1-Phenylpropyl)amino]adenosineHCID 53927112—

반응 조건

온도130 °C

반응 단계

In Scheme A, step b, the acetonide (2) is then treated with an appropriately substituted primary amine to provide the secondary amine of structure (3). More specifically, the acetonide (2) is combined with a large excess of an appropriately substituted primary amine, such as L-(-)-amphetamine, D-(+)-amphetamine, (R)-1-phenylpropylamine or (S)-1-phenylpropylamine, under an atmosphere of an inert gas such as nitrogen. The mixture is then heated to approximately 130° C. with stirring for approximately 3 to 6 hours. After cooling, the product can be isolated and purified by techniques well known to one skilled in the art. For example, the crude mixture can be directly purified by flash chromatography followed by radial chromatography using an appropriate eluent such as 3% to 6% methanol/chloroform to provide the secondary amine (3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05426101
출처 데이터셋uspto-grants-1995_06
ORD IDord-91a42dcf5ab743dabf4e25dc19f9830e
출처 메모uspto-grants-1995_06