3,4-dihydro-7-(4-((N-(4-ethoxycarbonylphenyl)carbamoyloxy)methyl)imidazolyl)-6-nitro-3-oxoquinoxaline-2-carboxylic acid

Base Information

Chemical Name:3,4-dihydro-7-(4-((N-(4-ethoxycarbonylphenyl)carbamoyloxy)methyl)imidazolyl)-6-nitro-3-oxoquinoxaline-2-carboxylic acid
CAS No.:221166-74-1
Molecular Formula:C₂₃H₁₈N₆O₉
Molecular Weight:522.431
Hs Code.:

Synonyms:3,4-dihydro-7-(4-((N-(4-ethoxycarbonylphenyl)carbamoyloxy)methyl)imidazolyl)-6-nitro-3-oxoquinoxaline-2-carboxylic acid

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Chemical Property of 3,4-dihydro-7-(4-((N-(4-ethoxycarbonylphenyl)carbamoyloxy)methyl)imidazolyl)-6-nitro-3-oxoquinoxaline-2-carboxylic acid

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Technology Process of 3,4-dihydro-7-(4-((N-(4-ethoxycarbonylphenyl)carbamoyloxy)methyl)imidazolyl)-6-nitro-3-oxoquinoxaline-2-carboxylic acid

There total 8 articles about 3,4-dihydro-7-(4-((N-(4-ethoxycarbonylphenyl)carbamoyloxy)methyl)imidazolyl)-6-nitro-3-oxoquinoxaline-2-carboxylic acid 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: 80.0%

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

: 221166-74-1
3,4-dihydro-7-(4-((N-(4-ethoxycarbonylphenyl)carbamoyloxy)methyl)imidazolyl)-6-nitro-3-oxoquinoxaline-2-carboxylic acid

Guidance literature:: With hydrogenchloride; acetic acid; at 20 ℃; for 24h;
DOI:10.1016/j.bmc.2005.05.030

Reference yield:

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

: 221166-74-1
3,4-dihydro-7-(4-((N-(4-ethoxycarbonylphenyl)carbamoyloxy)methyl)imidazolyl)-6-nitro-3-oxoquinoxaline-2-carboxylic acid

Guidance literature:: Multi-step reaction with 8 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

8: 80 percent / HCl; AcOH / 24 h / 20 °C

With hydrogenchloride; 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

: 221166-74-1
3,4-dihydro-7-(4-((N-(4-ethoxycarbonylphenyl)carbamoyloxy)methyl)imidazolyl)-6-nitro-3-oxoquinoxaline-2-carboxylic acid

Guidance literature:: Multi-step reaction with 5 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

5: 80 percent / HCl; AcOH / 24 h / 20 °C

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