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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573541Generated: October 30, 2026

Hydrochloric Acid → 4-Amino-3-bromo-2,6-dimethylthieno[2,3-b]pyridine-5-carboxylic acid

https://huagongshe.com/reaction/573541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 4-amino-3-bromo-2,6-dimethylthieno[2,3-b]pyridine-5-carboxylateHCID 68323712—
SolventEthanolHCID 702—
Product4-Amino-3-bromo-2,6-dimethylthieno[2,3-b]pyridine-5-carboxylic acidHCID 6832404565.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of ethyl 4-amino-3-bromo-2,6-dimethylthieno[2,3-b]pyridine-5-carboxylate (5 g, 15.19 mmol) (Description 6) in ethanol (50 mL) was added aqueous NaOH (3M) (20.25 mL, 60.8 mmol) and the mixture stirred at 100° C. for 1 h. The reaction mixture was cooled and combined with material (4.43 g) from a similar reaction. The combined solution was acidified with aqueous HCl (1M) to pH 6-7. Ethanol was removed in vacuo. Water (50 mL) was added and the mixture extracted with DCM (5×50 mL). The combined organics were dried over MgSO4, filtered and solvent removed in vacuo, to afford the title compound (2.98 g). LCMS (A) m/z: 301/303 [M+1]+, Rt 0.73 min (acidic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029545B2
Source datasetuspto-grants-2015_05
ORD IDord-f7f83ef3d8c14ae0a3a12ebac80611d4
Source noteuspto-grants-2015_05