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HRID 2354846作成日:2026年10月25日

Bromine → 9-Benzyl-8-bromo-2-methoxycarbonylmethylaminoadenine

https://huagongshe.com/reaction/2354846

反応式

関与物質

役割名称HCID仕込み量
反応物BromineHCID 24408—
反応物9-Benzyl-2-methoxycarbonylmethylaminoadenineHCID 23079428—
溶媒DichloromethaneHCID 6344—
生成物9-Benzyl-8-bromo-2-methoxycarbonylmethylaminoadenineHCID 23079440—

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-25818225884e405084030653495c4953
出典メモuspto-grants-2010_07