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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023704Generated: November 3, 2026

Cyanuric chloride → Methyl 4-[(4,5-diisopropylfuran-2-carbonyl)amino]benzoate

https://huagongshe.com/reaction/1023704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
ReactantTriethylamineHCID 8471—
ReactantMethyl 4-aminobenzoateHCID 12082—
Reactant4,5-Diisopropylfuran-2-carboxylic acidHCID 58420514—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetoneHCID 180—
ProductMethyl 4-[(4,5-diisopropylfuran-2-carbonyl)amino]benzoateHCID 6739553389.3%

Reaction Steps

A solution of 4,5-diisopropylfuran-2-carboxylic acid (50 mg, 0.255 mmol) and cyanuric chloride (71 mg, 0.385 mmol) in acetone (3 ml) was added with triethylamine (142 μl, 1.021 mmol), and the mixture was stirred at room temperature for 3.5 hours. The reaction mixture was added with methyl 4-aminobenzoate (77 mg, 0.510 mmol), and the mixture was further stirred for 14 hours. The reaction solvent was evaporated, then the residue was dissolved in pyridine (1 ml), the solution was added with 4-dimethylaminopyridine (1 mg, 8.20 μmol), and the mixture was stirred at room temperature for 4 hours. Pyridine was evaporated, and then the reaction mixture was dissolved in 10% methanol-chloroform, the solution was added with silica gel (1.0 g), and the mixture was evaporated to dryness. The residue was purified by silica gel chromatography [hexane-ethyl acetate (6:1)] to obtain methyl 4-[(4,5-diisopropylfuran-2-carbonyl)amino]benzoate (75 mg, 89%) as colorless prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722730B2
Source datasetuspto-grants-2014_05
ORD IDord-a939961a1e2345c4ad57a37bd8d47e01
Source noteuspto-grants-2014_05