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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572633Generated: October 30, 2026

Ammonium Hydroxide → 4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxamide

https://huagongshe.com/reaction/572633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acidHCID 58022862—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxamideHCID 58022896—

Reaction Steps

To a suspension of 4-cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid (2.85 g, 7.93 mmol) in methylene chloride (30 mL), were added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (3.28 g, 17.1 mmol) and 1-hydroxybenzotriazole (2.27 g, 16.8 mmol). The reaction mixture was stirred at room temperature for two hours and ammonium hydroxide (15.4 mL) was added and the biphasic mixture was stirred at room temperature for two hours. Water (100 mL), methanol (50 mL), methylene chloride (200 mL) was added. The organic layer was removed. The aqueous layer was extracted five times with a solution of 20% methanol in methylene chloride (100 mL). The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated to the title compound as dark red oil (1.47 g, 57%). LCMS: (FA) ES+ 325.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029411B2
Source datasetuspto-grants-2015_05
ORD IDord-a7188241bba94ed78bb586193bdc7912
Source noteuspto-grants-2015_05