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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063107Generated: November 1, 2026

Triethylamine → HCID 178469058, compound

https://huagongshe.com/reaction/1063107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 2,4-dioxovalerateHCID 69208—
Reactant2-CyanoethanethioamideHCID 1416277—
SolventEthanolHCID 702—
ProductHCID 178469058HCID 17846905864.5%

Reaction Steps

To a stirred solution of 2-cyanothioacetamide (3.52 g, 35 mmol) and ethyl 2,4-dioxovalerate (5.0 g, 32 mmol) in anhydrous EtOH (75 mL) at room temperature was added triethylamine (0.5 mL) and the reaction was stirred overnight. Filtration and washing of the precipitates with EtOH gave 3-cyano-2-mercapto-6-methyl-isonicotinic acid ethyl ester as a yellow solid (4.54 g, 64.5%). A mixture of this ester (3.54 g, 16 mmol), bromoacetamide (2.15 g, 16 mmol) and sodium ethoxide (2.18 g, 32 mmol) in MeOH was heated at reflux overnight. It was then allowed to cool to room temperature. Filtration and washing of the precipitates with EtOH provided 3-amino-2-carbamoyl-6-methyl-thieno[2,3-b]pyridine-4-carboxylic acid ethyl ester as a solid (0.94 g, 21.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964956B2
Source datasetuspto-grants-2005_11
ORD IDord-6453c069b1fa44aea0151af0aea4c235
Source noteuspto-grants-2005_11