The origin of a common compound about 56622-54-9

At the same time, in my other blogs, there are other synthetic methods of this type of compound,56622-54-9, (6-Methylpyridin-3-yl)methanamine, and friends who are interested can also refer to it.

With the rapid development and complex challenges of chemical substances, the synthesis of new drugs is usually one of the most effective ways to increase yield.56622-54-9, name is (6-Methylpyridin-3-yl)methanamine, molecular formula is C7H10N2, molecular weight is 122.17, as common compound, the synthetic route is as follows.Quality Control of (6-Methylpyridin-3-yl)methanamine

Into a round bottom flask were combined 5-formyl-4′-methylbiphenyl-3-carboxylic acid(3.00 g, 12.5 mmol), (6-methylpyridin-3-yl)methanamine (1.91 g, 15.6 mmol), NN-diisopropylethylamine (6.46 g, 49.9 mmol) and NN-dimethylformamide (97 mL). NN,N’,N’-Tetramethyl-O-(7-azabenzotriazol- l-yl)uronium hexafluorophosphate (9.50 g, 25.0 mmol) was added in one portion and the mixture was heated at 60 0C for 2 h. After cooling, the mixture was poured onto saturated sodium bicarbonate (200 mL) and extracted with ethyl acetate (3 x 100 mL). The combined extracts were dried over sodium sulfate and concentrated in vacuo. The residue was purified by column chromatography using methylene chloride:methanol gradient (0-10%) to afford the title compound. LC-MS: 346.2 [M+l ]+; 1H NMR (400 MHz, DMSO-d6): 10.14 (s, IH), 8.46-8.43 (m, 2H), 8.37-8.33 (m, 2H), 7.72 (d, 2H, J = 8.0 Hz), 7.64 (dd, IH, J = 8.0 Hz), 7.34 (d, 2H, J = 7.9 Hz), 7.22 (d, 2H, J = 7.9 Hz), 4.51 (d, 2H, J = 5.9 Hz), 2.44 (s, 3H), 2.37 (s, 3H).

At the same time, in my other blogs, there are other synthetic methods of this type of compound,56622-54-9, (6-Methylpyridin-3-yl)methanamine, and friends who are interested can also refer to it.

Reference:
Patent; RENOVIS, INC.; WO2009/110985; (2009); A2;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem