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tert-butyl 4-((4-(5-(methylsulfonyl)pyridin-2-yl)cyclohex-3-enyloxy)methyl)piperidine-1-carboxylate

Base Information
  • Chemical Name:tert-butyl 4-((4-(5-(methylsulfonyl)pyridin-2-yl)cyclohex-3-enyloxy)methyl)piperidine-1-carboxylate
  • CAS No.:1401098-40-5
  • Molecular Formula:C23H34N2O5S
  • Molecular Weight:450.599
  • Hs Code.:
tert-butyl 4-((4-(5-(methylsulfonyl)pyridin-2-yl)cyclohex-3-enyloxy)methyl)piperidine-1-carboxylate

Synonyms:tert-butyl 4-((4-(5-(methylsulfonyl)pyridin-2-yl)cyclohex-3-enyloxy)methyl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-((4-(5-(methylsulfonyl)pyridin-2-yl)cyclohex-3-enyloxy)methyl)piperidine-1-carboxylate
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Technology Process of tert-butyl 4-((4-(5-(methylsulfonyl)pyridin-2-yl)cyclohex-3-enyloxy)methyl)piperidine-1-carboxylate

There total 7 articles about tert-butyl 4-((4-(5-(methylsulfonyl)pyridin-2-yl)cyclohex-3-enyloxy)methyl)piperidine-1-carboxylate 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:
With sodium carbonate; tetrakis(triphenylphosphine) palladium(0); In water; N,N-dimethyl-formamide; at 100 ℃; for 1h; Inert atmosphere; Sealed tube; Microwave irradiation;
Guidance literature:
Multi-step reaction with 3 steps
1.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere
1.2: 2.5 h / -78 - 20 °C
2.1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 1 h / 100 °C / Inert atmosphere; Microwave irradiation
3.1: sodium carbonate / tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide; water / 1 h / 100 °C / Inert atmosphere; Sealed tube; Microwave irradiation
With potassium acetate; sodium carbonate; lithium hexamethyldisilazane; tetrakis(triphenylphosphine) palladium(0); dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; In tetrahydrofuran; water; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 6 steps
1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 72 h / 20 - 55 °C
2.1: hydrogen / palladium 10% on activated carbon / ethanol; water / 15 h / 23 °C / 760.05 Torr
3.1: hydrogen; sodium hydroxide / rhodium contaminated with carbon / water / 21 h / 60 - 70 °C / 7500.75 - 9750.98 Torr
3.2: 18 h / 23 °C
4.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere
4.2: 2.5 h / -78 - 20 °C
5.1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 1 h / 100 °C / Inert atmosphere; Microwave irradiation
6.1: sodium carbonate / tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide; water / 1 h / 100 °C / Inert atmosphere; Sealed tube; Microwave irradiation
With di-isopropyl azodicarboxylate; hydrogen; potassium acetate; sodium carbonate; triphenylphosphine; sodium hydroxide; lithium hexamethyldisilazane; tetrakis(triphenylphosphine) palladium(0); dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium 10% on activated carbon; rhodium contaminated with carbon; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide;
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