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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44839생성일: 2026년 10월 24일

(R)-2-(1-(8-cyclopentyl-7-ethyl-5-methyl-6-oxo-5,6,7,8-tetrahydropteridin-2-yl)-1H-imidazol-4-yl)acetonitrile → (R)-2-(4-(2-aminoethyl)-1H-imidazol-1-yl)-8-cyclopentyl-7-ethyl-5-methyl-7,8-dihydropteridin-6(5H)-one

https://huagongshe.com/ko/reaction/44839

반응식

참여 물질

역할이름HCID투입량
반응물(R)-2-(1-(8-cyclopentyl-7-ethyl-5-methyl-6-oxo-5,6,7,8-tetrahydropteridin-2-yl)-1H-imidazol-4-yl)acetonitrileHCID 58405740—
촉매Adams' catalystHCID 345198—
용매Ethyl AcetateHCID 8857—
생성물(R)-2-(4-(2-aminoethyl)-1H-imidazol-1-yl)-8-cyclopentyl-7-ethyl-5-methyl-7,8-dihydropteridin-6(5H)-oneHCID 5840589342.2%

반응 단계

(R)-2-(1-(8-cyclopentyl-7-ethyl-5-methyl-6-oxo-5,6,7,8-tetrahydropteridin-2-yl)-1H-imidazol-4-yl)acetonitrile (Example 35, 0.08 g, 0.218 mmol) and PtO2 (40 mg) were suspended in 2 mL of EtOAc and the resulting mixture was stirred under an atmosphere of hydrogen (1 atm, balloon) for 18 h. The resulting solution was filtered through Celite, concentrated, then purified by preparative HPLC to give the title compound (34 mg). LCMS: 370.1 m/z (M+H)+; ret. Time: 4.09 (Analytical Method C).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541418B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-375633b2085a4bb3a7a0ebd80fb12d18
출처 메모uspto-grants-2013_09