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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 845035생성일: 2026년 10월 23일

6-(Phenylmethoxy)-9H-purin-2-amine → HCID 14154536, 화합물

https://huagongshe.com/ko/reaction/845035

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참여 물질

역할이름HCID투입량
반응물6-(Phenylmethoxy)-9H-purin-2-amineHCID 4578—
반응물Sodium hydrideHCID 24758—
반응물HCID 10757649HCID 10757649—
반응물HCID 178418361HCID 178418361—
용매Acetic AcidHCID 176—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물HCID 14154536HCID 1415453625.4%

반응 조건

온도60 °C

반응 단계

A solution of 2.41 g (10 mmole) of 2-amino-6-benzyloxypurine [M. J. Robins and R. K. Robins, J. Org. Chem., 24, 2160 (1969)] in 24 ml of dry DMF was treated with 0.44 g (11 mmole) of sodium hydride (60% dispersion in oil). The mixture was stirred under nitrogen as hydrogen was evolved. After gas evolution had ceased and a clear solution had formed, a solution of 3.46 g (11 mmole) of (±)-3-(2,2-dimethyl-1,3-dioxolan-4-yl)propyl p-toluene-sulfonate (prepared as above) in 2 ml of DMF was added. The mixture was stirred at 60° C. for 3 days. The cooled mixture was then neutralized with glacial acetic acid and concentrated in vacuo. The residue was taken up in ethyl acetate, filtered, re-concentrated and chromatographed on silica gel (elution with ethyl acetate). Evaporation of fractions containing clean product gave a residue which, on trituration with ether, yielded 975 mg (25%) of white crystals, mp 111°-112° C. The analytical batch, similarly prepared, had m.p. 115.5°-118°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04755516
출처 데이터셋uspto-grants-1988_07
ORD IDord-7cabf6e2e6a64bd792398e990a961e79
출처 메모uspto-grants-1988_07