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N-methyl-2-(2-(2-(4-phenyl-1-piperidyl)ethoxy)phenyl)thiazolidine-3-carbothioamide oxalate

Base Information
  • Chemical Name:N-methyl-2-(2-(2-(4-phenyl-1-piperidyl)ethoxy)phenyl)thiazolidine-3-carbothioamide oxalate
  • CAS No.:107336-58-3
  • Molecular Formula:C24H31N3OS2
  • Molecular Weight:441.662
  • Hs Code.:
N-methyl-2-(2-(2-(4-phenyl-1-piperidyl)ethoxy)phenyl)thiazolidine-3-carbothioamide oxalate

Synonyms:N-methyl-2-(2-(2-(4-phenyl-1-piperidyl)ethoxy)phenyl)thiazolidine-3-carbothioamide oxalate

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Chemical Property of N-methyl-2-(2-(2-(4-phenyl-1-piperidyl)ethoxy)phenyl)thiazolidine-3-carbothioamide oxalate
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Technology Process of N-methyl-2-(2-(2-(4-phenyl-1-piperidyl)ethoxy)phenyl)thiazolidine-3-carbothioamide oxalate

There total 4 articles about N-methyl-2-(2-(2-(4-phenyl-1-piperidyl)ethoxy)phenyl)thiazolidine-3-carbothioamide oxalate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) K2CO3; 2.) 10percent HCl / 1.) DMF, 80 deg C, 22 h; 2.) H2O, MeOH, 70 deg C, 20 min
2: 1.) NaOH / 1.) EtOH, reflux, 1 h; 2.) reflux, 1.5 h
With hydrogenchloride; sodium hydroxide; potassium carbonate;
DOI:10.1248/cpb.35.2825
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) K2CO3; 2.) 10percent HCl / 1.) DMF, 80 deg C, 22 h; 2.) H2O, MeOH, 70 deg C, 20 min
2: 1.) NaOH / 1.) EtOH, reflux, 1 h; 2.) reflux, 1.5 h
With hydrogenchloride; sodium hydroxide; potassium carbonate;
DOI:10.1248/cpb.35.2825
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