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N-[2-(2-azidoethoxy)ethyl]-4-[3,5-dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyramide

Base Information Edit
  • Chemical Name:N-[2-(2-azidoethoxy)ethyl]-4-[3,5-dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyramide
  • CAS No.:948995-63-9
  • Molecular Formula:C23H27N5O6
  • Molecular Weight:469.497
  • Hs Code.:
  • Mol file:948995-63-9.mol
N-[2-(2-azidoethoxy)ethyl]-4-[3,5-dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyramide

Synonyms:N-[2-(2-azidoethoxy)ethyl]-4-[3,5-dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyramide

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Chemical Property of N-[2-(2-azidoethoxy)ethyl]-4-[3,5-dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyramide Edit
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Technology Process of N-[2-(2-azidoethoxy)ethyl]-4-[3,5-dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyramide

There total 9 articles about N-[2-(2-azidoethoxy)ethyl]-4-[3,5-dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyramide 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 azide; In N,N-dimethyl-formamide; at 20 ℃; for 12h;
DOI:10.1021/jo070621b
Guidance literature:
Multi-step reaction with 3 steps
1: CH2Cl2 / 3 h / 20 °C
2: pyridine / 12 h / 20 °C
3: 70 percent / NaN3 / dimethylformamide / 12 h / 20 °C
With pyridine; sodium azide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo070621b
Guidance literature:
Multi-step reaction with 4 steps
1: EDAC / CH2Cl2 / 3 h / 20 °C
2: CH2Cl2 / 3 h / 20 °C
3: pyridine / 12 h / 20 °C
4: 70 percent / NaN3 / dimethylformamide / 12 h / 20 °C
With pyridine; sodium azide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo070621b
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