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HRID 1089681作成日:2026年10月25日

Dimethylformamide → Acyclovirvalericester

https://huagongshe.com/reaction/1089681

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Valeryl chlorideHCID 61186—
反応物HCID 178508933HCID 178508933—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒Methanol--water (1/1)HCID 22242641—
生成物AcyclovirvalericesterHCID 13552452485.1%

反応条件

温度5 °C

反応手順

A mixture of acyclovir prepared according to UK Patent No. 1523865 (3.11 moles), 4-dimethylaminopyridine (4.91 moles) and dimethylformamide (5.6 L) was stirred under nitrogen with heating on steam bath to give a homogeneous solution. On cooling to room temperature valeryl chloride (4.91 moles) was added dropwise while the temperature was maintained at 20°-25° C. Progress of the reaction was monitored by HPLC (Partisil ODS-3, methanol:water 50:50) and the reaction was terminated when the level of residual acyclovir was less than 0.5% (AUC). The mixture was cooled to 5° C., filtered and the cake was washed with dimethylformamide (200 ml). The combined filtrates were diluted with absolute ethanol (1 L), stirred for two hours at ambient temperature and concentrated to a thick oil. Methanol (16 L) was added and the resulting suspension was refluxed for 1.5 hours, cooled to 5° C. and filtered. The crude product was washed with methanol (200 mL) and dried under vacuum to constant weight to give 819 g (85.1% yield) of 9-(2-valeryloxyethoxymethyl) guanine, M.p. 215°-217° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05079252
出典データセットuspto-grants-1992_01
ORD IDord-f7df73bf6c844dc890797c17757fe548
出典メモuspto-grants-1992_01