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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698960Generated: October 30, 2026

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

https://huagongshe.com/reaction/1698960

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butynoic acidHCID 68535—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
SolventDimethylformamideHCID 6228—
ProductN-(4-((3-bromophenyl)amino)-6-quinazolinyl)-2-butynamideHCID 2776—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 2-butynoic acid (196 mg, 2.3 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (385 mg, 2.0 mmol) in DMF (5 mL) stirring at 25° C. for 20 minutes was added 6-amino-4-[(3-bromophenyl)amino]quinazoline (316 mg, 1.0 mmol). The resulting solution was stirred under N2 at 25° C. for 14 hours further 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (206 mg, 1.0 mmol) and 2-butynic acid (82 mg, 1.0 mmol) were. After another 8 hours further, 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (197 mg, 1.0 mmol) and the acid (93 mg, 1.0 mmol) were added to the reaction. After stirring at 25° C. a further 12 hours, the reaction was quenched with water. The yellow precipitate was collected, sonicated with acetone, treated with triethyl amine and purified by preparative tlc on silica, eluting with 1:1 EtOAc/acetone. The desired product was isolated as a yellow solid (20 mg, 4.7%), mp 281-283° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344459B1
Source datasetuspto-grants-2002_02
ORD IDord-da35901dcb2742009bb9f842fe5cb0ef
Source noteuspto-grants-2002_02