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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188986Generated: October 29, 2026

3,5-Dimethyl-4-hydroxybenzonitrile → 4-(2-Chlorothieno[2,3-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

https://huagongshe.com/reaction/2188986

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dimethyl-4-hydroxybenzonitrileHCID 20176—
ReactantSodium hydrideHCID 24758—
Reactant2,4-Dichlorothieno[2,3-d]pyrimidineHCID 12217324—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Chlorothieno[2,3-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrileHCID 5784887828.1%

Reaction Steps

A stirred suspension of NaH (85 mg, 2.12 mmol) in dry THF (12 mL) was added 4-hydroxy-3,5-dimethyl benzonitrile (311 mg, 2.12 mmol) and stirred at room temperature for 30 min under Argon. The reaction mixture was added to a solution of 2,4-dichlorothieno[2,3-d]pyrimidine (434 mg, 2.12 mmol) in dry THF (10 mL) and heated at 50° C. for 2 h, the resulting mixture was diluted with water and washed with EtOAc. The combined organic layers were washed with water, brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (5:1) to give the product as a white solid (188 mg, 28%):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324223B2
Source datasetuspto-grants-2012_12
ORD IDord-2bb5e26a9de34c419907168e83f712fb
Source noteuspto-grants-2012_12