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214045-74-6

4-Chlorothiazolo[4,5-c]pyridine synthesis

3synthesis methods
Thiazolo[4,5-c]pyridine,  5-oxide

214045-73-5
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4-Chlorothiazolo[4,5-c]pyridine

214045-74-6
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Yield:214045-74-6 180 mg

Reaction Conditions:

with trichlorophosphate for 2 h;Reflux;

Steps:

535.2 Step 2

Compound 535a (400 mg, 2.61 mmol) was dissolved in phosphorus oxychloride (5 mE) and refluxed for 2 hours. The reaction was concentrated under reduced pressure and then quenched with saturated sodium bicarbonate solution and extracted with ethyl acetate. The combined organiclayers were dried over sodium sulfate and concentrated toprovide the desired product (180 mg). [M+H]171.1

References:

US9433621,2016,B2 Location in patent:Page/Page column 139; 140

139460-11-0 Synthesis
3-Amino-4-pyridinethiol hydrochloride (1:1)

139460-11-0
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4-Chlorothiazolo[4,5-c]pyridine

214045-74-6
32 suppliers
inquiry