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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063108Generated: November 1, 2026

2-Bromoacetamide → HCID 11778364, compound

https://huagongshe.com/reaction/1063108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoacetamideHCID 69632—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 178469058HCID 178469058—
SolventMethanolHCID 887—
ProductHCID 11778364HCID 1177836421.1%

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-a61bb737fb0a4720a8fbbac87e1f1e7c
Source noteuspto-grants-2005_11