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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505584Generated: November 4, 2026

Bromine → 5-Methoxy[1,3]thiazolo[5,4-b]pyridin-2-amine

https://huagongshe.com/reaction/505584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant6-Methoxy-3-pyridinylamineHCID 81121—
ReactantPotassium thiocyanateHCID 516872—
SolventAcetic AcidHCID 176—
Product5-Methoxy[1,3]thiazolo[5,4-b]pyridin-2-amineHCID 2801557—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 6-methoxy-pyridin-3-ylamine (5.0 g, 0.0403 mol) in 10 mL of acetic acid is added slowly to a solution of potassium thiocyanate (20 g, 0.205 mol) in 100 mL of acetic acid at 0° C. followed by a solution of bromine (2.5 mL, 0.0488 mol) in 5 mL of acetic acid. The reaction is stirred for 2 h at 0° C. and then allowed to warm to RT. The resulting solid is collected by filtration and washed with acetic acid, then partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The insoluble material is removed by filtration and the organic layer is evaporated and dried to afford 5-methoxy-thiazolo[5,4-b]pyridin-2-ylamine as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781451B2
Source datasetuspto-grants-2010_08
ORD IDord-3cdf78ba52a94fce8c0d70e5b174411d
Source noteuspto-grants-2010_08