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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194659Generated: October 26, 2026

Sodium hydride → HCID 178467752, compound

https://huagongshe.com/reaction/1194659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3,9-Dihydro-1,3-dimethyl-8-((phenylmethyl)amino)-1H-purine-2,6-dioneHCID 100382—
Reactantbeta-Ethoxyethylmalonic acidHCID 17872155—
SolventDimethylformamideHCID 6228—
ProductHCID 178467752HCID 178467752—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred suspension of 7.43 g of 8-benzylaminotheophylline in 104 ml of dry N,N-dimethyl-formamide add portionwise over 10 minutes 1.19 g of a 60% dispersion of sodium hydride. Heat the mixture to 50° C. under a nitrogen atmosphere for 30 minutes. Add 13.30 g of the diethyl ester of β-ethoxyethylmalonic acid. Heat the mixture to 150° C. under a nitrogen atmosphere for approximately 37 hours. Allow the system to cool to room temperature and remove the solvent in vacuo. Add a mixture of water:chloroform (1:2.5) to the resulting semisolid. Acidify the aqueous portion with 3M HCl. Extract the product from the aqueous portion with chloroform. Wash the chloroform extracts with brine, dry over anhydrous sodium sulfate, filter and remove the solvent in vacuo to give the crude product. Triturate the crude product with ether. Purify the crude product by column chromatography on silica gel and triturate the major fraction with hexane to give the title compound, mp 156.5°-157.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816458
Source datasetuspto-grants-1989_03
ORD IDord-8dc92f6df62c41b88a5e1289fc339d0b
Source noteuspto-grants-1989_03