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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341795Generated: October 25, 2026

Propentofylline → A 802715

https://huagongshe.com/reaction/341795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropentofyllineHCID 4938—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418332HCID 178418332—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductA 802715HCID 129959—

Reaction Steps

22.4 g (0.3 mol) of methylmagnesium chloride in the form of a 20% strength solution in tetrahydrofuran are added dropwise with vigorous stirring at room temperature to a suspension of 61.3 g (0.2 mol) of 3-methyl-1-(5-oxohexyl)-7-propylxanthine in 2 l of anhydrous ether, the internal temperature rising to approximately 30° C. The mixture is then warmed with stirring and under reflux for 2 hours, treated with saturated aqueous ammonium chloride solution to decompose the alkoxide formed, and the organic phase is separated off and washed twice with 500 ml of water each time. The collected water phases are extracted thoroughly with dichloromethane again. The dichloromethane extract is combined with the ethereal phase, dried over sodium sulfate, filtered and evaporated under reduced pressure, 59.0 g of crude product (91.5% of theory) being obtained, which is purified by recrystallization from diisopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856330
Source datasetuspto-grants-1999_01
ORD IDord-515242502e904265b5d301b58b4800f4
Source noteuspto-grants-1999_01