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tert-butyl 4-(4-{(5S)-5-[(acetyl amino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenoxy)piperidine-1-carboxylate

Base Information
  • Chemical Name:tert-butyl 4-(4-{(5S)-5-[(acetyl amino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenoxy)piperidine-1-carboxylate
  • CAS No.:346664-40-2
  • Molecular Formula:C22H30FN3O6
  • Molecular Weight:451.495
  • Hs Code.:
tert-butyl 4-(4-{(5S)-5-[(acetyl amino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenoxy)piperidine-1-carboxylate

Synonyms:tert-butyl 4-(4-{(5S)-5-[(acetyl amino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenoxy)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(4-{(5S)-5-[(acetyl amino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenoxy)piperidine-1-carboxylate
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Technology Process of tert-butyl 4-(4-{(5S)-5-[(acetyl amino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenoxy)piperidine-1-carboxylate

There total 10 articles about tert-butyl 4-(4-{(5S)-5-[(acetyl amino)methyl]-2-oxo-1,3-oxazolidin-3-yl}-2-fluorophenoxy)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:
Multi-step reaction with 8 steps
1.1: 89 percent / KOtBu / tetrahydrofuran / 0 - 20 °C
2.1: ammonium formate / 10 percent Pd/C / methanol / 2 h / Heating
3.1: 2.06 g / NaHCO3 / acetone; H2O / 6 h / 20 °C
4.1: n-BuLi / tetrahydrofuran / 1 h / -78 °C
4.2: 72 percent / tetrahydrofuran / -78 - 20 °C
5.1: triethylamine / CH2Cl2 / 3 h / 0 °C
6.1: 2.07 g / sodium azide / dimethylformamide / 75 °C
7.1: triphenylphosphine / tetrahydrofuran / 3 h / 20 °C
7.2: H2O / 4 h / 60 °C
8.1: 1.85 g / pyridine / ethyl acetate / 20 °C
With pyridine; n-butyllithium; sodium azide; potassium tert-butylate; ammonium formate; sodium hydrogencarbonate; triethylamine; triphenylphosphine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; acetone;
DOI:10.1016/S0968-0896(02)00065-2
Guidance literature:
Multi-step reaction with 8 steps
1.1: 89 percent / KOtBu / tetrahydrofuran / 0 - 20 °C
2.1: ammonium formate / 10 percent Pd/C / methanol / 2 h / Heating
3.1: 2.06 g / NaHCO3 / acetone; H2O / 6 h / 20 °C
4.1: n-BuLi / tetrahydrofuran / 1 h / -78 °C
4.2: 72 percent / tetrahydrofuran / -78 - 20 °C
5.1: triethylamine / CH2Cl2 / 3 h / 0 °C
6.1: 2.07 g / sodium azide / dimethylformamide / 75 °C
7.1: triphenylphosphine / tetrahydrofuran / 3 h / 20 °C
7.2: H2O / 4 h / 60 °C
8.1: 1.85 g / pyridine / ethyl acetate / 20 °C
With pyridine; n-butyllithium; sodium azide; potassium tert-butylate; ammonium formate; sodium hydrogencarbonate; triethylamine; triphenylphosphine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; acetone;
DOI:10.1016/S0968-0896(02)00065-2
Guidance literature:
Multi-step reaction with 7 steps
1.1: ammonium formate / 10 percent Pd/C / methanol / 2 h / Heating
2.1: 2.06 g / NaHCO3 / acetone; H2O / 6 h / 20 °C
3.1: n-BuLi / tetrahydrofuran / 1 h / -78 °C
3.2: 72 percent / tetrahydrofuran / -78 - 20 °C
4.1: triethylamine / CH2Cl2 / 3 h / 0 °C
5.1: 2.07 g / sodium azide / dimethylformamide / 75 °C
6.1: triphenylphosphine / tetrahydrofuran / 3 h / 20 °C
6.2: H2O / 4 h / 60 °C
7.1: 1.85 g / pyridine / ethyl acetate / 20 °C
With pyridine; n-butyllithium; sodium azide; ammonium formate; sodium hydrogencarbonate; triethylamine; triphenylphosphine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; acetone;
DOI:10.1016/S0968-0896(02)00065-2
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