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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509957Generated: October 30, 2026

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

https://huagongshe.com/reaction/1509957

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 numberUS08211898B2
Source datasetuspto-grants-2012_07
ORD IDord-7623926c3ea140358bd01f84292446c7
Source noteuspto-grants-2012_07