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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677562Generated: November 1, 2026

Triethylamine → HCID 67215740, compound

https://huagongshe.com/reaction/1677562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantImidazo(1,5-a)pyridineHCID 274090—
ReactantMethyl 5-(chlorocarbonyl)-2-nitrobenzoateHCID 12350504—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 67215740HCID 67215740—

Reaction Steps

5.6 g (0.023 mol) of methyl 5-(chlorocarbonyl)-2-nitrobenzoate and 3.4 ml (0.024 mol) of triethylamine are added to 1.3 g (0.011 mol) of imidazo[1,5-a]pyridine [described in J. Chem. Soc., (1955), 2834-2836] dissolved in 100 ml of 1,2-dichloroethane. The mixture is stirred at ambient temperature for 4 hours. The reaction medium is concentrated under reduced pressure and then the residue is taken up in dichloromethane and a saturated aqueous sodium bicarbonate solution. The organic phase is separated by settling, washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated under reduced pressure. The product is purified by column chromatography on silica gel, elution being carried out with dichloromethane. After evaporation, 3.1 g of a yellow solid are collected. Melting point: 151° C.; 1H NMR (d6-DMSO): 3.92 (3H, s), 7.39-7.42 (1H, m), 7.50-7.54 (1H, m), 8.00 (1H, s), 8.10 (1H, d), 8.25 (1H, d), 8.69 (1H, d), 8.76 (1H, s), 9.78 (1H, d)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008321B2
Source datasetuspto-grants-2011_08
ORD IDord-fe62d2f98c864e2a900aaec5cb679378
Source noteuspto-grants-2011_08