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HRID 2354845作成日:2026年10月26日

Diisopropylethylamine → 9-Benzyl-2-methoxycarbonylmethylaminoadenine

https://huagongshe.com/reaction/2354845

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Glycine methyl ester hydrochlorideHCID 122755—
反応物9-Benzyl-2-chloro-9h-purin-6-amineHCID 276482—
溶媒1-ButanolHCID 263—
生成物9-Benzyl-2-methoxycarbonylmethylaminoadenineHCID 2307942817.2%

反応条件

温度150 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07754728B2
出典データセットuspto-grants-2010_07
ORD IDord-24eff1f5a667456288f6171685348f26
出典メモuspto-grants-2010_07