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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244459Generated: October 29, 2026

Dimethylformamide → 5-Allyl-3-methyl-3,5-dihydropyrrolo[3,2-d]pyrimidin-4-one

https://huagongshe.com/reaction/244459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5-allyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 59437321—
SolventWaterHCID 962—
Product5-Allyl-3-methyl-3,5-dihydropyrrolo[3,2-d]pyrimidin-4-oneHCID 5943727764%

Reaction Steps

To a room temperature solution of 5-allyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidine (220 mg, 1.3 mmol, 1 equiv.) in 3 mL of DMF was added 60% NaH (100 mg, 2.5 mmol, 2 equiv.) followed by MeI (0.18 ml, 1.8 mmol, 1.5 equiv.). After 30 minutes, the mixture was diluted with water and extracted with EtOAc. The combined organic layers were dried, filtered, and concentrated in vacuo. The residue was purified by reverse phase HPLC (5-90% CH3CN/water+0.1% TFA). The desired fractions were combined and concentrated to remove CH3CN. The remaining aqueous mixture was extracted with EtOAc, dried, filtered, and evaporated to provide 152 mg (64%) of 5-allyl-3-methyl-3,5-dihydropyrrolo[3,2-d]pyrimidin-4-one as a yellow oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658637B2
Source datasetuspto-grants-2014_02
ORD IDord-7b18bbcdd92f4a0c9ff57180fd1089fb
Source noteuspto-grants-2014_02