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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274665Generated: October 29, 2026

N-Hydroxysuccinimide → 4-[3-(4,5-Dibromothenoylamino)propylthio]pyridine

https://huagongshe.com/reaction/274665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxysuccinimideHCID 80170—
Reactant4,5-Dibromothenoic acidHCID 80611—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-(3-Aminopropylthio)pyridineHCID 15227695—
SolventDichloromethaneHCID 6344—
Product4-[3-(4,5-Dibromothenoylamino)propylthio]pyridineHCID 1523149471.8%

Reaction Steps

To a solution of 2.55 g (8.91 mmol) of 4,5-dibromothiophene-2-carboxylic 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 2.79 g of the desired compound (yield: 71.8%, colorless powder).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389658
Source datasetuspto-grants-1995_02
ORD IDord-4364be282ffe458daa5215a9ec3098d8
Source noteuspto-grants-1995_02