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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614551Generated: October 26, 2026

Methanol → 2-(Hydroxymethyl)pyrazolo(1,5-c)quinazolin-5(6H)-one

https://huagongshe.com/reaction/614551

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—
Product2-(Hydroxymethyl)pyrazolo(1,5-c)quinazolin-5(6H)-oneHCID 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 numberUS04145420
Source datasetuspto-grants-1979_03
ORD IDord-1250957b1fde4157add8598c644ccc16
Source noteuspto-grants-1979_03