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3-c]pyridine synthesis

4synthesis methods
3-c]pyridine

1357946-60-1
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Yield:-

Reaction Conditions:

with hydrogen;palladium 10% on activated carbon in tetrahydrofuran;ethanol at 20; for 24 h;

Steps:



A solution of 4-chloro-6-methyl-1 H-pyrazolo[4,3-c]pyridine [1159828-70-2] (750 mg, 4.48 mmol) in a mixture of ethanol (25 mL) and THF (10 mL) was hydrogenated over 10% Pd/C (75 mg, 0.07 mmol) at RT for 24 h. The reaction mixture was filtered, the catalyst was washed with ethanol and the filtrate was concentrated under vacuum. MS (LC-MS): 134 [M+H]+, tR (HPLC conditions k): 0.23 min.

References:

WO2012/93101,2012,A1 Location in patent:Page/Page column 159

1005515-30-9 Synthesis
4-chloro-6-methylnicotinoyl chloride

1005515-30-9
2 suppliers
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3-c]pyridine

1357946-60-1
15 suppliers
inquiry