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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073011Generated: November 2, 2026

Sodium Hydroxide → Thieno[3,4-c]pyridine-6-carboxylic acid

https://huagongshe.com/reaction/1073011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl thieno[3,4-c]pyridine-6-carboxylateHCID 22047039—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductThieno[3,4-c]pyridine-6-carboxylic acidHCID 2204706497%

Reaction Steps

Methyl thieno[3,4-c]pyridine-6-carboxylate (250 mg, 1.3 mmol) is dissolved in MeOH (7 ml) and water (1 ml). 2M NaOH (0.72 ml, 1.43 mmol) is added drop-wise. The reaction is stirred overnight at rt and is monitored by TLC. The volatiles are removed in vacuo and the residue is dissolved in water (2 ml). 10% HCl is used to adjust the pH to 3, and the reaction again stirred overnight at rt. The aqueous solution is extracted repeatedly with EtOAc (20×10 ml). The combined organics are dried over MgSO4, filtered, and concentrated to a yellow solid. The amount of isolated product via extraction is minimal (67 mg), so the aqueous layer is concentrated and found to contain the majority of product. Extraction of the solid aqueous residue with EtOAc provided 225 mg (97%) of thieno[3,4-c]pyridine-6-carboxylic acid as a yellow solid. MS (EI) m/z: 179 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911543B2
Source datasetuspto-grants-2005_06
ORD IDord-95392ac12a63496fb6391400764123b1
Source noteuspto-grants-2005_06