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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516839Generated: October 27, 2026

2,4,6-Trimethylphenol → 5-benzyl-4-(mesityloxy)-5H-pyrrolo[3,2-d]pyrimidin-2-amine

https://huagongshe.com/reaction/1516839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylphenolHCID 10698—
ReactantSodium hydrideHCID 24758—
Reactant5-benzyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-2-amineHCID 57693617—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product5-benzyl-4-(mesityloxy)-5H-pyrrolo[3,2-d]pyrimidin-2-amineHCID 5769366250.1%

Reaction Steps

To a stirred suspension of NaH (56 mg, 2.33 mmol) in dry NMP (2 mL) was added 2,4,6-trimethyl phenol (317 mg, 2.33 mmol). The mixture was stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 5-benzyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-2-amine (200 mg, 0.78 mmol) in dry NMP (1.5 mL) and the resulting solution was heated at 90° C. for 16 h. After completion of the reaction, the reaction mixture was diluted with water and washed with EtOAc. The combined organic layers were washed with water, 2% NaOH, and brine and dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (3:1) to give the product as a white solid (140 mg, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227601B2
Source datasetuspto-grants-2012_07
ORD IDord-3c576f605b2b4a1e9240eac56eab6a07
Source noteuspto-grants-2012_07