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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075299Generated: October 30, 2026

Sodium hydride → Proquazone

https://huagongshe.com/reaction/1075299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 13061754HCID 13061754—
ReactantHCID 178418255HCID 178418255—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductProquazoneHCID 31508—

Reaction Steps

To a suspension of 1.8 g sodium hydride in 25 ml tetrahydrofurane are added portionwise 13.08 g 1-isopropyl-7-methyl-quinazolin-2,4(1H,3H)-dione under constant release of hydrogen. 40 ml of a 2N solution of phenylmagnesiumbromide in tetrahydrofurane are added dropwise at 40° C. to the clear solution and the resulting suspension stirred at 40° for 15 hours. Water is added and the solvent is evaporated in vacuo. The residue is taken up with methylene chloride and 30 ml 12% hydrochloric acid. The organic layer is concentrated to give the title compound (recrystallized from toluene), m.p. 140°-143°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04395550
Source datasetuspto-grants-1983_07
ORD IDord-4609b38c685a4b229706e34472730ad9
Source noteuspto-grants-1983_07