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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30418Generated: October 25, 2026

Ethanol → Ethyl 3-aminothieno[2,3-b]pyridine-2-carboxylate

https://huagongshe.com/reaction/30418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
ReactantEthyl ThioglycolateHCID 12185—
Reactant2-ChloronicotinonitrileHCID 81079—
SolventWaterHCID 962—
ProductEthyl 3-aminothieno[2,3-b]pyridine-2-carboxylateHCID 73845993.2%

Reaction Steps

A mixture of 2-chloro-3-cyanopyridine (330 g), ethyl 2-mercaptoacetate (361.2 g), sodium carbonate (265 g) and EtOH (1.2L) was heated to reflux for 4.5 hours. It was then cooled to ambient temperature, added to water (10 L) and the addition was washed in with water (5 L). The resulting slurry was stirred for 30 minutes and then it was filtered. The filter cake was washed with two portions of water (2×2.5 L) and dried at the pump. The solids were then dried to constant weight under vacuum at 45° C. to yield the title compound as a brown solid (493.1 g, 93.2%). δH (CDCl3) 8.68 (1H, dd, J 4.7, 1.2 Hz), 7.93 (1H, dd, J 8.5, 1.2 Hz), 7.29 (1H, dd, J 8.5, 4.7 Hz), 5.90 (2H, b), 4.38 (2H, q, J 7.0 Hz), 1.40 (3H, t, J 7.0 Hz). LCMS RT 2.9 minutes, 223 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423047B2
Source datasetuspto-grants-2008_09
ORD IDord-958b7b90ea0c45cf995308ff1817ed7e
Source noteuspto-grants-2008_09