Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

6-[(1-methylpiperidin-4-yl)oxy]pyridin-3-amine synthesis

3synthesis methods
2-(1-methylpiperidin-4-yl)oxy-5-nitropyridine

944401-78-9
2 suppliers
inquiry

6-[(1-methylpiperidin-4-yl)oxy]pyridin-3-amine

944401-79-0
9 suppliers
inquiry

-

Yield:944401-79-0 860 mg

Reaction Conditions:

with palladium 10% on activated carbon;hydrogen in methanol at 35; under 760.051 Torr;

Steps:

22.2 Step 22.2: 6-(1 -Methylpiperidin-4-yloxy)pyridin-3-ylamine

Step 22.2: 6-(1 -Methylpiperidin-4-yloxy)pyridin-3-ylamine 1.05 g of the compound obtained in step 20.1 are dissolved in 90 ml of MeOH and then hydrogenated at atmospheric pressure at 35°C over 10% Pd/C. The medium is filtered and then evaporated under reduced pressure to give 860 mg of 6-(1 - methylpiperidin-4-yloxy)pyridin-3-ylamine.

References:

WO2013/111106,2013,A1 Location in patent:Page/Page column 109