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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350611Generated: November 3, 2026

L-Glutamine → 4-carbamoyl-2-(6-methoxy-4H-quinazolin-3-yl)butanoic acid

https://huagongshe.com/reaction/350611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-GlutamineHCID 5961—
ReactantSodium borohydrideHCID 4311764—
ReactantN-(2-formyl-4-methoxyphenyl)formamideHCID 21088389—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
Product4-carbamoyl-2-(6-methoxy-4H-quinazolin-3-yl)butanoic acidHCID 21088385—

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 0.79 g of the product from stage 3 in 30 ml of methanol was added to a solution of 0.58 g of L-glutamine in 10 ml of methanol and 2 ml of 2N sodium hydroxide solution. After stirring for 1 hour at 20° C., the mixture was cooled to 0° C. and 0.103 g of sodium borohydride was added in portions within 30 minutes. The mixture was stirred for 12 hours at 0° C., then adjusted to pH 2 to 3, and stirred for a further 4 hours at 20° C. After neutralizing the solution with sodium hydroxide, the methanol was distilled off. The aqueous residue was washed twice with 15 ml of diethyl ether each time, and then concentrated by evaporation in vacuo. The residue was taken up in 25 ml of methanol and freed from insoluble constituents by filtration. The residue obtained by evaporating the filtrate in vacuo was directly reacted further as described in stage 5, without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183274B2
Source datasetuspto-grants-2007_02
ORD IDord-be8db5e7db014e8587df42f2c21fd59c
Source noteuspto-grants-2007_02