Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257817Generated: October 26, 2026

Triethylamine → HCID 178441839, compound

https://huagongshe.com/reaction/257817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantValeryl chlorideHCID 61186—
Reactant2-Amino-5-methylbenzoic acidHCID 76255—
ReactantEthyl acetate hexaneHCID 21226206—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 178441839HCID 17844183925%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3.0 g (20 mmol) of 2-amino-5-methyl benzoic acid in 20 mL of dry DMF at 0° C. was added 200 mg of DMAP followed by 6.07 g (60 mmol) of triethylamine and 5.02 g (40 mmol) of valeryl chloride. The resulting mixture was stirred at 0° C. for 30 min. The mixture was heated to 110° C. and monitored by TLC for the formation of the intermediate quinoxazolone (Rf =0.8, 40% EtOAc/hexane). Following complete formation of the intermediate 10 g (100 mmol) of (NH4)2CO3 was added cautiously. Heating was continued to ensure consumption of the quinoxazolone and formation of the polar (Rf =0.4, 40% EtOAc/hexane) quinazolin-4(1H)-one. The reaction mixture was concentrated in vacuo and the residue was taken up in 50 mL of ether and 50 mL of water. The mixture was filtered and the filtrate discarded after washing the residue with 20 mL of ether. The residue was recrystalized from MeOH to give 1.07 g (25%) of the title compound as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05264439
Source datasetuspto-grants-1993_11
ORD IDord-9a69dc4fbdaf476db95ddb091e96a5a9
Source noteuspto-grants-1993_11