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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 6-Methoxy-3-pyridinylamine | HCID 81121 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Methoxy[1,3]thiazolo[5,4-b]pyridin-2-amine | HCID 2801557 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750020B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-767a867ae2bc42d3a36ea76c32b82b1a |
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| Source note | uspto-grants-2010_07 |
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