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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353339Generated: October 29, 2026

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

https://huagongshe.com/reaction/2353339

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 numberUS07750020B2
Source datasetuspto-grants-2010_07
ORD IDord-767a867ae2bc42d3a36ea76c32b82b1a
Source noteuspto-grants-2010_07