HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488914Generated: October 30, 2026
2-Bromoacetamide → HCID 11778364, compound
https://huagongshe.com/reaction/488914
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromoacetamide | HCID 69632 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 178469058 | HCID 178469058 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11778364 | HCID 11778364 | 21.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06974870B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-52e307143c4140d497be0a5192124438 |
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| Source note | uspto-grants-2005_12 |
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