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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35836Generated: October 23, 2026

Sodium hydride → Fenazaquin

https://huagongshe.com/en/reaction/35836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-ChloroquinazolineHCID 78864—
Reactantp-tert-Butylphenethyl alcoholHCID 79410—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductFenazaquinHCID 8635628.4%

Reaction Steps

To a solution of 1.1 g of sodium hydride in 50 ml of DMF, 4.0 g of 2-[4-(t-butyl)phenyl]ethanol was added, and the mixture was stirred at room temperature for one hour. Then 3.6 g of 4-chloroquinazoline in 20 ml of DMF were added, and the mixture was stirred at room temperature overnight. The mixture was then poured into a mixture of ice in water. The product was extracted into CH2Cl2, and the resulting solution was concentrated to dryness. TLC showed one major spot and five minor spots. The product was purified by HPLC (silica gel, CH2Cl2). The fractions containing the major product were collected and concentrated, giving 1.9 g of the title product. Yield: 28.4%. M.P. 70°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411963
Source datasetuspto-grants-1995_05
ORD IDord-378409998bb94c5480b3bbf142ebb392
Source noteuspto-grants-1995_05