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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361482Generated: October 25, 2026

Dimethyl Sulfoxide → 3-Methyl-7-(methylpivaloyl)xanthine

https://huagongshe.com/reaction/361482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
Reactant3-MethylxanthineHCID 70639—
Reactant4-Chloro-2,2-dimethylbutanoateHCID 21753047—
SolventWaterHCID 962—
Product3-Methyl-7-(methylpivaloyl)xanthineHCID 2158423390.2%

Reaction Steps

This example illustrates a synthesis of 1-(11,10-Oxidoundecanyl)-3-methyl-7-methylpivalylxanthine (inventive compound no. 1412). A mixture of 3-methylxanthine (Aldrich, 1.00 g, 6.0 mmol), sodium hydride (145 mg, 6.0 mmol) and dimethyl sulfoxide (20 mL) was stirred until homogeneous (0.5 hours). Chloromethylpivalate (865 mL, 904 mg, 6.0 mmol) was added and the reaction stirred for 18 hours. The reaction mixture was poured into water (70 mL) and then extracted with 25% ethano/dichloromethane (4×60 mL). The combined organic extracts were dried over sodium sulfate and evaporated under vacuum to a volume of 40 mL. This solution was cooled in icewater, whereupon a thick white precipitate formed. The solid was filtered off under suction and dried under vacuum to yield 1.43 g (90% yield) 3-methyl-7-(methylpivaloyl)xanthine (inventive compound no. 1404).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866576
Source datasetuspto-grants-1999_02
ORD IDord-2177ddf5787b4adfb9a33a5cc43679ce
Source noteuspto-grants-1999_02