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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068992Generated: October 30, 2026

4-Methylmorpholine → Isopropyl-methyl-amino-but-2-ynoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide

https://huagongshe.com/reaction/1068992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
ReactantIsopropyl-methyl-amino-but-2-ynoic acidHCID 21190750—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductIsopropyl-methyl-amino-but-2-ynoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amideHCID 8675705240.4%

Reaction Steps

Isobutyl chloroformate (0.845 g, 6.2mmol) and N-methylmorpholine (1.0 g, 9.9 mmol) were added to an ice cold solution of 1.5 g (9.67 mmol) of isopropyl-methyl-amino-but-2-ynoic acid in 70 mL of tetrahydrofuran under nitrogen. After stirring for 30 min, a solution of 1.500 g of N-(3-bromophenyl)-4,6-quinazolindiamine in 15 mL of pyridine was added and the mixture was stirred for 2 hr at 0° C. The reaction was then quenched with ice water, poured into saturated sodium bicarbonate, and the product was extracted with ethyl acetate. Chromatography of the extract on silica gel, eluting with methanol/ethyl acetate (15:85), gave 0.870 g of isopropyl-methyl-amino-but-2-ynoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide: mass spectrum (m/e): M+H 452.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251912B1
Source datasetuspto-grants-2001_06
ORD IDord-482ef4ddf1a34241a03f9f9a65d96501
Source noteuspto-grants-2001_06