Category: 1062580-52-2

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.1062580-52-2,(3R,4R)-1-Benzyl-N,4-dimethylpiperidin-3-amine dihydrochloride,as a common compound, the synthetic route is as follows.

Add SMA 11.0kg, SMB 12.8kg, DIPEA 19.5kg, DMSO to a 200L reactor50.0 kg, 15.0 kg of purified water, and the temperature was raised to 107C. After the reaction is complete, add 24.0kg absolute ethanol to room temperature and addWater 30.0kg, stirring and decrystallization 2h, suction filtration, drying at 60±5C, 17.2kg of white solid. Yield 93.0%, SMB residue0.3%, HPLC purity 98.9%.

1062580-52-2, The synthetic route of 1062580-52-2 has been constantly updated, and we look forward to future research findings.

Reference：
Patent; Yangzijiang Pharmaceutical Group Co., Ltd.; Xiao Can; Xu Jingren; Cai Wei; Zhu Xiaohe; Zhang Haibo; Lv Huimin; Hu Tao; Wu Jianhua; Gu Cheng; Xu Chenjun; (12 pag.)CN107793418; (2018); A;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem

1062580-52-2, (3R,4R)-1-Benzyl-N,4-dimethylpiperidin-3-amine dihydrochloride is a piperidines compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

100 gm of 4-Chloro-7H-pyrrolo[2,3-d] pyrimidine and 205 gm of (3R,4R)-l-benzyl-N-4- dim ethyl piperidin-3-amine dihydrochloride, 216 gm of Potassium carbonate was dissolved in water and raise the temperature of about 90.0C. After the end of the reaction, extract the product into Toluene and filter off. Distill off the solvent completely under vacuum and isolated the product in Isopropyl alcohol. Filtered the material and dried to get 145 gm of N-((3R,4R)-l-benzyl-4-methylpiperidin-3-yl)-N- methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine., 1062580-52-2

The synthetic route of 1062580-52-2 has been constantly updated, and we look forward to future research findings.

Reference：
Patent; PHALANX LABS PRIVATE LIMITED; AVIRNENI, Sri Ramakrishna; (26 pag.)WO2018/172821; (2018); A1;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem