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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1920601생성일: 2026년 10월 26일

(2R)-5-(Benzyloxycarbonylamino)-2-[(R)-3-benzyloxytetradecanoylamino]pentan-1-ol → (2R)-5-amino-2-[(R)-3-benzyloxytetradecanoylamino]pentan-1-ol

https://huagongshe.com/reaction/1920601

반응식

참여 물질

역할이름HCID투입량
반응물(2R)-5-(Benzyloxycarbonylamino)-2-[(R)-3-benzyloxytetradecanoylamino]pentan-1-olHCID 16086982—
반응물EtOH EthanolHCID 57419690—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매triethylamine TriethylamineHCID 22592508—
생성물(2R)-5-amino-2-[(R)-3-benzyloxytetradecanoylamino]pentan-1-olHCID 11476040—

반응 단계

In a three-neck flask, the catalyst (150 mg of 20% palladium/carbon) was added to the solution of (2R)-5-(benzyloxycarbonylamino)-2-[(R)-3-benzyloxytetradecanoylamino]pentan-1-ol (3.0 g; 5.27 mmol) in a mixture of triethylamine Et3N (6 ml)/HPLC-grade ethanol EtOH (300 ml). Air was discharged under vacuum then the flask was loaded with hydrogen. The reaction mixture was hydrogenated at room temperature for 2 hours then the catalyst was filtered off and the filtrate was concentrated to provide the desired product as a homogenous white solid. Rf=0.2, 5/1 0/0.5 CH2Cl2-MeOH-Et3N, m.p.=47-48° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08173133B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-2bc368e9abfa493bb09096be0109c576
출처 메모uspto-grants-2012_05