Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408947Generated: November 2, 2026

Triethylamine → 2-(4-Chlorobenzoylamino)-4,5-dimethoxybenzamide

https://huagongshe.com/reaction/2408947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
Reactant2-Amino-4,5-dimethoxybenzamideHCID 10867236—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Chlorobenzoylamino)-4,5-dimethoxybenzamideHCID 22997405—

Reaction Steps

As shown in scheme Q, 2-amino-4,5-dimethoxybenzamide is reacted with 4-chlorobenzoyl chloride in presence of triethyl amine and THF to give 2-((4-chlorophenyl)carbonylamino)-4,5-dimethoxybenzamide. Which is cyclised using NaOH and then treated with thionyl chloride to give 4-chloro-2-(4-chlorophenyl)-6,7-dimethoxyquinazoline (McKee, R. L. et. al., J. Am. Chem. Soc., 1946, 68, 1902-1903). The 4-chlorocompound is treated with 5-(tert-butyl)selenophene-2-carboxamide in the presence of NaOH/DMF to give 3-(2-(4-chlorophenyl)-6,7-dimethoxyquinazolin-4-ylamino)-5-tert-butylselenophene-2-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815879B2
Source datasetuspto-grants-2014_08
ORD IDord-7e9afdc42e0b4a639d5b0bd5c9bb03a6
Source noteuspto-grants-2014_08