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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347904Generated: October 26, 2026

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

https://huagongshe.com/reaction/347904

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 (1.2 L) 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° 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 numberUS07176215B2
Source datasetuspto-grants-2007_02
ORD IDord-93162a166d40405db2cbce305f16bb2d
Source noteuspto-grants-2007_02