Analyzing the synthesis route of 55052-27-2

At the same time, in my other blogs, there are other synthetic methods of this type of compound,55052-27-2, 6-Chloro-1H-pyrrolo[2,3-b]pyridine, 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.55052-27-2, name is 6-Chloro-1H-pyrrolo[2,3-b]pyridine, molecular formula is C7H5ClN2, molecular weight is 152.581, as common compound, the synthetic route is as follows.Computed Properties of C7H5ClN2

4 g (0.03 mol) of aluminum trichloride, 3 ml of dichloromethane and 3.6 g (0.02 mol), i.e. 2.23 ml, of trichloroacetyl chloride are placed in a round-bottomed flask with a condenser, a magnetic stirrer and a calcium chloride guard tube, and the mixture is stirred at room temperature for 30 minutes. 1.52 g (0.01 mol) of 6-chloro-1H-pyrrolo[2,3-b]pyridine are added portionwise and the mixture is refluxed for 3 hours. While cooling in an ice bath, 50 ml of ice are added to the flask and the mixture is stirred vigorously for 30 minutes. A pasty mass is obtained, which is separated from the aqueous phase by decantation. The product is used directly in the next step.

At the same time, in my other blogs, there are other synthetic methods of this type of compound,55052-27-2, 6-Chloro-1H-pyrrolo[2,3-b]pyridine, and friends who are interested can also refer to it.

Reference:
Patent; SANOFI-AVENTIS; US2005/182062; (2005); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem