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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2354845생성일: 2026년 10월 26일

Diisopropylethylamine → 9-Benzyl-2-methoxycarbonylmethylaminoadenine

https://huagongshe.com/reaction/2354845

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 번호US07754728B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-24eff1f5a667456288f6171685348f26
출처 메모uspto-grants-2010_07