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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1684980생성일: 2026년 10월 27일

Diisopropylethylamine → 9-Benzyl-2-methoxycarbonylmethylaminoadenine

https://huagongshe.com/reaction/1684980

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Glycine methyl ester hydrochlorideHCID 122755—
반응물9-Benzyl-2-chloro-9h-purin-6-amineHCID 276482—
용매1-ButanolHCID 263—
생성물9-Benzyl-2-methoxycarbonylmethylaminoadenineHCID 2307942817.2%

반응 조건

온도150 °C

반응 단계

9-Benzyl-2-chloroadenine (0.30 g, 1.12 mmol), glycine methyl ester hydrochloride (0.72 g, 5.73 mmol) and diisopropylethylamine (1.48 g, 11.47 mmol) were added to n-butanol (10 ml), and the mixture was stirred in an autoclave at 150° C. for 19 hours. The solvent was removed and the residue was poured into water. The solution was extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, concentrated and the residue was purified by column chromatography to give 9-benzyl-2-methoxycarbonylmethylaminoadenine (0.06 g) as a brown tar. Thus obtained 9-benzyl-2-methoxycarbonylmethylaminoadenine was dissolved in dichloromethane (10 ml) and to the solution was added bromine (0.05 ml) in an ice bath. The mixture was stirred at room temperature for 1 hour. After removing the solvent, the residue was poured into water and extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, concentrated and the residue was purified by column chromatography to give 9-benzyl-8-bromo-2-methoxycarbonylmethylaminoadenine (0.06 g) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08148371B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-770ac510b2ce4e798d8f6746dec3db29
출처 메모uspto-grants-2012_04