Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984432Generated: October 29, 2026

HOAt → N-tert-butyl-N'-[3-methoxy-4-(5-oxazolyl)phenyl]oxalamide

https://huagongshe.com/reaction/984432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHOAtHCID 181649—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(tert-Butylamino)(oxo)acetic acidHCID 5187990—
Reactant3-Methoxy-4-(oxazol-5-yl)anilineHCID 15462732—
SolventDichloromethaneHCID 6344—
ProductN-tert-butyl-N'-[3-methoxy-4-(5-oxazolyl)phenyl]oxalamideHCID 979702680.7%

Reaction Steps

A solution of 95 mg (0.5 mmol) of 3-methoxy-4-(5-oxazolyl)aniline, 73 mg (0.5 mmol) of N-tert-butyloxalamic acid, 134 mg (0.7 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 75 mg (0.55 mmol) of 1-hydroxy-7-azabenzotriazole in 4 ml of dichloromethane was stirred a room temperature for 18 hours. The resulting mixture was washed with 2M hydrochloric acid and saturated sodium bicarbonate, dried over magnesium sulphate and evaporated to dryness. The residue was triturated with petrol and collected by filtration to give 128 mg of N-tert-butyl-N′-[3-methoxy-4-(5-oxazolyl)phenyl]oxalamide as a pale yellow solid. MS: 318 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867299B2
Source datasetuspto-grants-2005_03
ORD IDord-4836aff1aa1545d1b2b98fb7deb706d8
Source noteuspto-grants-2005_03