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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6124Generated: October 26, 2026

5-Methylthiophene-2-carboxylic acid → 4-[3-(5-Methylthenoylamino)propylthio]pyridine

https://huagongshe.com/reaction/6124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methylthiophene-2-carboxylic acidHCID 74713—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-(3-Aminopropylthio)pyridineHCID 15227695—
SolventDichloromethaneHCID 6344—
Product4-[3-(5-Methylthenoylamino)propylthio]pyridineHCID 1907923864.5%

Reaction Steps

To a solution of 1.27 g (8.91 mmol) of 5-methyl-2-thiophenecarboxylic acid and 1.33 g (11.6 mmol) of N-hydroxysuccinimide in 90 ml of methylene chloride, 2.05 g (10.7 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added under ice-cooling with stirring. The mixture was stirred at room temperature for 1 hour. Further, 1.50 g (8.91 mmol) of 4-(3-aminopropylthio)pyridine was added, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was washed with water and dried, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain powder. The powder thus obtained was washed with ether and dried to obtain 1.68 g of the desired compound (yield: 64.5%, colorless powder).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246948
Source datasetuspto-grants-1993_09
ORD IDord-dc6dda4f6f4f4e49bffbd2ffd2ad92b8
Source noteuspto-grants-1993_09