HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23615Generated: October 25, 2026
Methyl iodide → Ethyl 2-formyl-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxylate
https://huagongshe.com/reaction/23615
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-formyl-3-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxylate | HCID 22574402 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-formyl-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxylate | HCID 22574293 | 69% |
Reaction Steps
A mixture of ethyl 2-formyl-3-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxylate (1.06 g, 3.99 mmol), potassium carbonate (826 mg, 5.98 mmol) and methyl iodide (1.24 mL, 19.9 mmol) in DMF (30 mL) was stirred at 50° C. for 24 hours. The mixture was diluted with water (60 mL), stirred with ice bath cooling for 5 minutes, and then filtered. The collected solid was washed with water and dried in vacuo, leaving a pale tan solid (764 mg, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852731B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-6e3d6b61685e491599d71390efa43156 |
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| Source note | uspto-grants-2005_02 |
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