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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50336Generated: November 1, 2026

Hydrochloric Acid → 2-Methoxymethyl-thiazolo[5,4-b]pyridin-6-yl-carboxylic acid

https://huagongshe.com/reaction/50336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-methoxymethyl-thiazolo[5,4-b]pyridine-6-carboxylateHCID 18412416—
SolventEthanolHCID 702—
Product2-Methoxymethyl-thiazolo[5,4-b]pyridin-6-yl-carboxylic acidHCID 18412439—

Reaction Steps

A mixture of 1.1 g (4.62 mmol) of methyl-2-methoxymethylthiazolo[5,4-b]pyridine-6-carboxylate and 9.2 mL of 2N sodium hydroxide solution were stirred into 50 mL of ethanol for one hour at room temperature. Then 9.2 mL of 2N hydrochloric acid were added, the alcohol was distilled off, and it was diluted with 20 mL of water. The aqueous phase was acidified with concentrated hydrochloric acid whilst cooling with ice, the beige precipitate formed was filtered off, then washed with water and dried. Yield: 1.03 g (100% of theory); Rf value: 0.10 (silica gel; ethyl acetate/petroleum ether=3:7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710055B2
Source datasetuspto-grants-2004_03
ORD IDord-71ae40c96c0c4e09b62a60be1f2d0b35
Source noteuspto-grants-2004_03