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ChemicalBook CAS DataBase List 3-(AMINOMETHYL)-4-ETHYL-6-METHYLPYRIDIN-2(1H)-ONE HCL
1346576-04-2

3-(AMINOMETHYL)-4-ETHYL-6-METHYLPYRIDIN-2(1H)-ONE HCL synthesis

3synthesis methods
2(1H)-Pyridinone, 3-(aminomethyl)-4-ethyl-6-methyl-

1346576-05-3
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3-(AMINOMETHYL)-4-ETHYL-6-METHYLPYRIDIN-2(1H)-ONE HCL

1346576-04-2
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Yield:1346576-04-2 86%

Reaction Conditions:

with hydrogenchloride in 1,4-dioxane;dichloromethane at 0; for 0.166667 h;

Steps:

5.4

Step 43-(Aminomethy])-4-ethyl-6-methylpyridin-2(lH)-one hydrochloride3-(Amino methyl)-4-ethyl-6-methylpyridin-2(lH)-one, (5.6 g, 33 mmol) was suspended in DCM (560 mL) and the insoluble contents/particles were filtered. The filtrate was concentrated and dried. The residue was dissolved in DCM (10 mL) and 4 M HCI inl,4-dioxane (16 mL, 66 mmol) was added at 0 °C and stirred for 10 min, at which time the reaction mixture was concentrated under high- vacuum and dried. The resulting crude solid was triturated with hexane (150 mL) and filtered. The solid was dried under vacuum. Collected 3-(amino methyl)-4-ethyl-6-methylpyridin-2(lH)-one hydrochloride (5.9 g, 86%). ? NMR (400 MHz, DMSO-6) δ ppm 1.082-1.120 (t, 3H, J = 7.6 Hz), 2.179 (s, 3H), 2.503-2.544 (m, 2H), 3.785-3.798 (d, 2H, J = 5.2 Hz), 6.024 (s,lH),7.985 (broad s,2H), 11.858 (broad s,lH). MS(ES) [M+H]+ 167.2.

References:

WO2011/140325,2011,A1 Location in patent:Page/Page column 146