With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.74879-18-8,(S)-(+)-2-Methylpiperazine,as a common compound, the synthetic route is as follows.,74879-18-8
To a solution of (S)-2-methylpiperazine (10 g, 100 mmol, eq) in EtOH (200 ml_) was added DIPEA (43.58 ml_, 250 mmol, 2.5 eq) and BOC20 (21.8 ml_, 100 mmol, 1 eq) at RT, then the reaction mixture was continued for 16 h. TLC analysis indicated formation of a less polar spot. The reaction mixture was concentrated to crude compound, which was diluted with water and extracted with EtOAc (3×100 ml_). The combined organic layer was dried over Na2S04 then concentrated to give (S)-tert-butyl 3-methylpiperazine- 1 -carboxylate (18 g, 90%) as a colorless oil.
As the paragraph descriping shows that 74879-18-8 is playing an increasingly important role.
Reference:
Patent; ONTARIO INSTITUTE FOR CANCER RESEARCH (OICR); AL-AWAR, Rima; ISAAC, Methvin; CHAU, Anh My; MAMAI, Ahmed; WATSON, Iain; PODA, Gennady; SUBRAMANIAN, Pandiaraju; WILSON, Brian; UEHLING, David; (191 pag.)WO2019/119145; (2019); A1;,
Piperazine – Wikipedia
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