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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448161Generated: October 31, 2026

Methanol → Pirquinozol

https://huagongshe.com/reaction/1448161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant5,6-Dihydro-5-oxopyrazolo[1,5-c]quinazoline-2-carboxylic acid ethyl esterHCID 136023344—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductPirquinozolHCID 13544934099.1%

Reaction Steps

A suspension of 3.84 g (0.015 mole) of 5,6-dihydro-5-oxopyrazolo[1,5-c]quinazoline-2-carboxylic acid ethyl ester prepared as described in part A above is stirred in 150 ml of tetrahydrofuran under nitrogen at room temperature. There is added 24 ml (0.034 mole) of a 20% solution of diisobutyl aluminum hydride in hexane. The resultant solution is stirred for 1 hour at room temperature whereupon 50 ml of methanol is added and the reaction mixture refluxed for 1 hour. The precipitate of aluminum alkoxide is filtered, air dried and Soxhlet extracted for 48 hours with boiling methanol. The extract is combined with the above filtrate and stripped to give 3.2 g of a white solid (quantitative yield). Recrystallization from methanol gives 2.7 g of pure title compound, m.p. 285°-287°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179561
Source datasetuspto-grants-1979_12
ORD IDord-857425db4bed4dbcb81bf517a3c17695
Source noteuspto-grants-1979_12