The origin of a common compound about 4,6-Dichloropyrimidine

The chemical industry reduces the impact on the environment during synthesis 1193-21-1, I believe this compound will play a more active role in future production and life.

Electric Literature of 1193-21-1, 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.1193-21-1, name is 4,6-Dichloropyrimidine, molecular formula is C4H2Cl2N2, molecular weight is 148.9781, as common compound, the synthetic route is as follows.

To a solution of 4, 6-dichloro-pyrimidine (10.0 g) in THF (10 mL) were added iPr2NEt (10.4 g) and 50% aqueous MezNH (6.05 g). The mixture was stirred at ambient temperature for 28 hr and poured into saturated aqueous NaHCO3. The aqueous layer was extracted with CHC13 (three times). The combined organic layer was dried over MgS04, filtered, and concentrated under reduced pressure. The residue was suspended in Et20. The precipitate was collected by filtration, washed with Et2O and dried under reduced pressure to give (6-chloro-pyrimidin-4-yl) -dimethyl-amine (6.37 g). ESI MS m/e 157, M ; IH NMR (300 MHz, CDC13) 6 3.12 (s, 6 H), 6.41 (s, 1 H), 8.37 (s, 1 H).

The chemical industry reduces the impact on the environment during synthesis 1193-21-1, I believe this compound will play a more active role in future production and life.

Reference:
Patent; TAISHO PHARMACEUTICAL CO., LTD.; Arena Pharmaceuticals, Inc; WO2005/95357; (2005); A2;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia