ethyl 3-ethoxy-7-[4-((4-ethoxycarbonylphenylamino)carbonyloxymethyl)imidazol-1-yl]-6-nitroquinoxaline-2-carboxylate

Base Information

Chemical Name:ethyl 3-ethoxy-7-[4-((4-ethoxycarbonylphenylamino)carbonyloxymethyl)imidazol-1-yl]-6-nitroquinoxaline-2-carboxylate
CAS No.:221166-33-2
Molecular Formula:C₂₇H₂₆N₆O₉
Molecular Weight:578.538
Hs Code.:

Synonyms:ethyl 3-ethoxy-7-[4-((4-ethoxycarbonylphenylamino)carbonyloxymethyl)imidazol-1-yl]-6-nitroquinoxaline-2-carboxylate

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Chemical Property of ethyl 3-ethoxy-7-[4-((4-ethoxycarbonylphenylamino)carbonyloxymethyl)imidazol-1-yl]-6-nitroquinoxaline-2-carboxylate

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Technology Process of ethyl 3-ethoxy-7-[4-((4-ethoxycarbonylphenylamino)carbonyloxymethyl)imidazol-1-yl]-6-nitroquinoxaline-2-carboxylate

There total 7 articles about ethyl 3-ethoxy-7-[4-((4-ethoxycarbonylphenylamino)carbonyloxymethyl)imidazol-1-yl]-6-nitroquinoxaline-2-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:

Reference yield: 100.0%

: 30806-83-8
p-ethoxycarbonylphenyl isocyanate

: 221164-29-0
ethyl 3-ethoxy-7-[4-(hydroxymethyl)imidazol-1-yl]-6-nitroquinoxaline-2-carboxylate

: 221166-33-2
ethyl 3-ethoxy-7-[4-((4-ethoxycarbonylphenylamino)carbonyloxymethyl)imidazol-1-yl]-6-nitroquinoxaline-2-carboxylate

Guidance literature:: In benzene; for 2h; Heating;
DOI:10.1016/j.bmc.2005.05.030

Reference yield:

: 364-78-3
2-nitro-4-fluoroaniline

: 221166-33-2
ethyl 3-ethoxy-7-[4-((4-ethoxycarbonylphenylamino)carbonyloxymethyl)imidazol-1-yl]-6-nitroquinoxaline-2-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: 88 percent / toluene / 24 h / Heating

2: 31 percent / potassium tert-butoxide / dimethylformamide / 1.5 h / 0 °C

3: 75 percent / PBr₃ / dimethylformamide / 1.5 h / 20 °C

4: 45 percent / AcOH; HNO₃ / 2 h / 80 °C

5: 68 percent / silver(I) oxide / toluene / 2 h / 100 °C

6: 43 percent / triethylamine / acetonitrile / 16 h / Heating

7: 100 percent / benzene / 2 h / Heating

With potassium tert-butylate; nitric acid; phosphorus tribromide; acetic acid; triethylamine; silver(l) oxide; In N,N-dimethyl-formamide; toluene; acetonitrile; benzene;
DOI:10.1016/j.bmc.2005.05.030

Reference yield:

: 55496-01-0
7-fluoro-3,4-dihydro-3-oxo-2-quinoxalinecarboxylic acid,ethyl ester

: 221166-33-2
ethyl 3-ethoxy-7-[4-((4-ethoxycarbonylphenylamino)carbonyloxymethyl)imidazol-1-yl]-6-nitroquinoxaline-2-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: 45 percent / AcOH; HNO₃ / 2 h / 80 °C

2: 68 percent / silver(I) oxide / toluene / 2 h / 100 °C

3: 43 percent / triethylamine / acetonitrile / 16 h / Heating

4: 100 percent / benzene / 2 h / Heating

With nitric acid; acetic acid; triethylamine; silver(l) oxide; In toluene; acetonitrile; benzene;
DOI:10.1016/j.bmc.2005.05.030