6-(3-tert-butyl-ureido)-2-(2-methoxy-5-nitro-benzylsulfanyl)-3-propyl-3H-benzoimidazole-4-carboxylic acid

Base Information

Chemical Name:6-(3-tert-butyl-ureido)-2-(2-methoxy-5-nitro-benzylsulfanyl)-3-propyl-3H-benzoimidazole-4-carboxylic acid
CAS No.:853655-28-4
Molecular Formula:C₂₄H₂₉N₅O₆S
Molecular Weight:515.59
Hs Code.:

6-(3-<i>tert</i>-butyl-ureido)-2-(2-methoxy-5-nitro-benzylsulfanyl)-3-propyl-3<i>H</i>-benzoimidazole-4-carboxylic acid

Synonyms:6-(3-tert-butyl-ureido)-2-(2-methoxy-5-nitro-benzylsulfanyl)-3-propyl-3H-benzoimidazole-4-carboxylic acid

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Chemical Property of 6-(3-tert-butyl-ureido)-2-(2-methoxy-5-nitro-benzylsulfanyl)-3-propyl-3H-benzoimidazole-4-carboxylic acid

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Technology Process of 6-(3-tert-butyl-ureido)-2-(2-methoxy-5-nitro-benzylsulfanyl)-3-propyl-3H-benzoimidazole-4-carboxylic acid

There total 6 articles about 6-(3-tert-butyl-ureido)-2-(2-methoxy-5-nitro-benzylsulfanyl)-3-propyl-3H-benzoimidazole-4-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: 91.0%

: 853655-27-3
6-(3-tert-butyl-ureido)-2-(2-methoxy-5-nitro-benzylsulfanyl)-3-propyl-3H-benzoimidazole-4-carboxylic acid methyl ester

: 853655-28-4
6-(3-tert-butyl-ureido)-2-(2-methoxy-5-nitro-benzylsulfanyl)-3-propyl-3H-benzoimidazole-4-carboxylic acid

Guidance literature:: With sodium hydroxide; In methanol; at 65 ℃;
DOI:10.1016/j.bmcl.2005.03.030

Reference yield:

: 853655-45-5
3,5-dinitro-2-propylamino-benzoic acid methyl ester

: 853655-28-4
6-(3-tert-butyl-ureido)-2-(2-methoxy-5-nitro-benzylsulfanyl)-3-propyl-3H-benzoimidazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 100 percent / H₂ / Pd/C / ethyl acetate / 20 °C

2: 100 percent / N,N-diisopropylethylamine / ethanol / 60 °C

3: 98 percent / Et₃N / tetrahydrofuran / 40 °C

4: 72 percent / N,N-diisopropylethylamine / 20 °C

5: 91 percent / aq. NaOH / methanol / 65 °C

With sodium hydroxide; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; ethyl acetate;
DOI:10.1016/j.bmcl.2005.03.030

Reference yield:

: 2213-79-8
methyl 2-chloro-3,5-dinitrobenzoate

: 853655-28-4
6-(3-tert-butyl-ureido)-2-(2-methoxy-5-nitro-benzylsulfanyl)-3-propyl-3H-benzoimidazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1: 89 percent / CH₂Cl₂ / 20 °C

2: 100 percent / H₂ / Pd/C / ethyl acetate / 20 °C

3: 100 percent / N,N-diisopropylethylamine / ethanol / 60 °C

4: 98 percent / Et₃N / tetrahydrofuran / 40 °C

5: 72 percent / N,N-diisopropylethylamine / 20 °C

6: 91 percent / aq. NaOH / methanol / 65 °C

With sodium hydroxide; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; ethyl acetate;
DOI:10.1016/j.bmcl.2005.03.030