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N-(4-aminophenyl)-2-piperidin-1-ylacetamide synthesis

4synthesis methods
-

Yield:100450-98-4 98%

Reaction Conditions:

with palladium 10% on activated carbon;hydrogen in ethyl acetate; under 1810.07 - 1965.21 Torr;

Steps:

N-(3-Aminophenyl)-3-(dimethylamino)propanamide (15a)

General procedure: To a solution of 14a (4.7 g, 20 mmol) in EA, 10% Pd/C (1.0 g) was suspended. The mixture was hydrogenated at 35 psi overnight. The reaction mixture was filtered through a pad of Celite. The filter cake was washed successively with EA and methanol. The combined filtrate and washings were evaporated in vacuo and dried to give 15a as a brown gum. Yield: 3.9 g (94%)

References:

Tala, Satishkumar D.;Ou, Tai-Hsin;Lin, Yi-Wen;Tala, Kiranben S.;Chao, Shu-Hsin;Wu, Ming-Hsi;Tsai, Tung-Hu;Kakadiya, Rajesh;Suman, Sharda;Chen, Ching-Huang;Lee, Te-Chang;Su, Tsann-Long [European Journal of Medicinal Chemistry,2014,vol. 76,p. 155 - 169] Location in patent:supporting information