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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430494Generated: October 30, 2026

4-Methylmorpholine → N-(4-((3-bromophenyl)amino)-6-quinazolinyl)-2-butynamide

https://huagongshe.com/reaction/430494

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant2-Butynoic acidHCID 68535—
ReactantN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-((3-bromophenyl)amino)-6-quinazolinyl)-2-butynamideHCID 277655.3%

Reaction Steps

A solution of 0.50 g of 2-butynoic acid in 10 ml of tetrahydrofuran was cooled in an ice bath. A 0.79 ml portion of isobutyl chloroformate followed by a 0.66 ml portion of N-methyl morpholine were added. After about 1 minute a solution of 1.6 g of N-(3-bromophenyl)-4,6-quinazolindiamine in 10 ml of pyridine was added. The reaction was allowed to come to room temperature and stir overnight. The solvents were removed at reduced pressure and the solid was recrystallized from n-butanol to give 1.07 g of N-[4-[(3-bromophenyl)amino]-6-quinazolinyl)-2-butynamide: mass spectrum (m/e): 381, 383.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323209B1
Source datasetuspto-grants-2001_11
ORD IDord-be17a86decdd4ca89b9aee296451dc21
Source noteuspto-grants-2001_11