Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736317Generated: October 30, 2026

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

https://huagongshe.com/reaction/736317

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 numberUS07595324B2
Source datasetuspto-grants-2009_09
ORD IDord-2e5df11d727d41038035243a2da3f400
Source noteuspto-grants-2009_09