With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.208167-83-3,tert-Butyl 4-(2-chloroethyl)piperazine-1-carboxylate,as a common compound, the synthetic route is as follows.
Example 15.1.2: Preparation of 4-[2-(2-Amino-benzoimidazol-l-yl)-ethyl]- piperazine-1-carboxylic acid tert-butyl ester; 4-[2-(2-Amino-benzoimidazol-l-yl)-ethyl]-piperazine-l-carboxylic acid tert-butyl ester was prepared according to the procedure described in WO2005/058869. 1H NMR (300MHz, CDCl3): delta 7.43 (IH, d, J = 7.5 Hz, Ar-CH), 7.17-7.06 (3H, m, Ar- CH), 5.78 (2H, s, NH2), 3.64 (2H, t, J = 5.7 Hz, NCH2CH2N), 3.46 (4H, m, CH2NCH2), 2.56 (4H, m, CH2NCH2), 2.43 (2H, t, J = 5.7 Hz, NCH2CH2N), 1.46 (9H, s, C[CH3J3).
208167-83-3 tert-Butyl 4-(2-chloroethyl)piperazine-1-carboxylate 22106269, apiperazines compound, is more and more widely used in various fields.
Reference£º
Patent; AVEXA LIMITED; WO2008/77188; (2008); A1;,
Piperazine – Wikipedia
Piperazines – an overview | ScienceDirect Topics