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!

1903-68-0

N,N-DIMETHYLPIPERIDINE-4-CARBOXAMIDE synthesis

4synthesis methods
-

Yield:1903-68-0 530 mg

Reaction Conditions:

with palladium 10% on activated carbon;hydrogen in ethanol;ethyl acetate at 10 - 35; for 5 h;

Steps:

1.C C) N,N-dimethylpiperidine-4-carboxamide

C)
N,N-dimethylpiperidine-4-carboxamide
Benzyl 4-(dimethylcarbamoyl)piperidine-1-carboxylate (960 mg) was dissolved in ethanol (15 mL) and ethyl acetate (15 mL), 10% palladium carbon (96 mg) was added thereto, and the mixture was stirred at room temperature for 5 hr under hydrogen atmosphere.
The insoluble substance was removed by filtration, and the filtrate was concentrated under reduced pressure to give the title compound (530 mg).
1H NMR (300 MHz, DMSO-d6) δ 1.31-1.57 (4H, m), 2.45 (1H, d, J = 3.0 Hz), 2.63 (1H, tt, J = 11.1, 4.0 Hz), 2.79 (3H, s), 2.91 (2H, dt, J = 12.1, 3.0 Hz), 2.99 (3H, s), 3.29 (2H, brs).

References:

EP2933247,2015,A1 Location in patent:Paragraph 0303