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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108754Generated: October 30, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-(3-Methoxybenzyl)-5-bromothiophene-3-carboxamide

https://huagongshe.com/reaction/2108754

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant3-MethoxybenzylamineHCID 21156—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant5-Bromothiophene-3-carboxylic acidHCID 12039978—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-(3-Methoxybenzyl)-5-bromothiophene-3-carboxamideHCID 57421982—

Reaction Steps

5-Bromothiophene-3-carboxylic acid (70%) (200 mg, 0.6 mmol of monobromide) was dissolved in DMF with 3-methoxybenzyl amine (0.3 g, 2.2 mmol), EDCI (0.42 g, 2.2 mmol), and HOBt hydrate (0.06 g, 0.4 mmol). The reaction mixture was stirred at room temperature for 3 days, diluted with EtOAc and the organic layer washed with 10% citric acid, saturated sodium bicarbonate, and brine. The organic layer was then dried over sodium sulfate and concentrated to an oil, which was purified by column chromatography on silica (10 to 30 5 EtOAc/hexanes) to give the product as a colorless oil, 195 mg, 0.6 mmol, 100%. 1H NMR 500 MHz (CDCl3) 7.81 (1H, s), 7.35 (1H, s), 7.28 (1H, m), 6.93 (1H, m), 6.87 (2H, m), 6.23 (1H, br s), 4.57 (2H, d), 3.84 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514448B2
Source datasetuspto-grants-2009_04
ORD IDord-a2454307d0784adb8946134a70311ebe
Source noteuspto-grants-2009_04