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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190319Generated: November 4, 2026

Lithium hydroxide, monohydrate → (1,3)Thiazolo(4,5-c)pyridin-2-amine

https://huagongshe.com/reaction/2190319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantN-(thiazolo[4,5-c]pyridin-2-yl)acetamideHCID 15593545—
SolventMethanolHCID 887—
Product(1,3)Thiazolo(4,5-c)pyridin-2-amineHCID 14252938—

Reaction Steps

To a suspension of N-(thiazolo[4,5-c]pyridin-2-yl)acetamide, prepared in the previous step, in MeOH (200 mL) at room temperature was added lithium hydroxide hydrate (7.08 g, 169 mmol). The reaction mixture was stirred at room temperature for 30 min and then warmed to 40° C. After 3 h, additional lithium hydroxide hydrate (7.48 g) was added. The reaction mixture was heated to 50° C. for 20 h and concentrated. The reaction mixture was diluted with DCM/MeOH (˜10:1, 500 mL). The undissolved material was removed by filtration and the filtrate was concentrated. Purification by flash column chromatography on silica gel (eluted with 2% to 10% MeOH in DCM) gave thiazolo[4,5-c]pyridin-2-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324396B2
Source datasetuspto-grants-2012_12
ORD IDord-85f87b6daa354f8dbe35c680bc789d31
Source noteuspto-grants-2012_12