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ChemicalBook CAS DataBase List THIAZOLO[4,5-B]PYRIDINE
273-98-3

THIAZOLO[4,5-B]PYRIDINE synthesis

3synthesis methods
-

Yield:273-98-3 53%

Reaction Conditions:

with copper(l) iodide;potassium sulfide;ammonium acetate in water at 140; for 11 h;Schlenk technique;Inert atmosphere;

Steps:

13 Example 13

Add 2-amino-3-iodopyridine (0.2 mmol), potassium sulfide (0.6 mmol), dimethyl sulfoxide (2 mL), cuprous iodide (0.04 mmol), and ammonium acetate to the dry Schlenk reaction tube in sequence (1.2 mmol) and water (80 ul). After the sample is added, vacuum with an oil pump and inject nitrogen for gas replacement. After three replacements, the reaction is stopped at 140°C for 11 hours and then cooled to room temperature. The reaction is detected by thin-layer chromatography (TLC). After the reaction of the raw materials is completed, the reaction is terminated, and the mixed solution in the reaction tube is cooled to room temperature. Preliminary treatment of the mixed solution: passing through a short column, extracting, collecting the organic layer, spinning powder, and performing column chromatography to obtain the target product with a yield of 52%.

References:

CN111892553,2020,A Location in patent:Paragraph 0072-0074

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