5-(1-benzoyl-2-methyl-3-isothioureido)-1-imidazole-4-carboxamide

Base Information

Chemical Name:5-(1-benzoyl-2-methyl-3-isothioureido)-1-imidazole-4-carboxamide
CAS No.:153887-21-9
Molecular Formula:C₂₂H₂₃N₅O₃S
Molecular Weight:437.522
Hs Code.:

5-(1-benzoyl-2-methyl-3-isothioureido)-1-<o-(2-hydroxyethyl)benzyl>imidazole-4-carboxamide

Synonyms:

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Chemical Property of 5-(1-benzoyl-2-methyl-3-isothioureido)-1-imidazole-4-carboxamide

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Technology Process of 5-(1-benzoyl-2-methyl-3-isothioureido)-1-imidazole-4-carboxamide

There total 5 articles about 5-(1-benzoyl-2-methyl-3-isothioureido)-1-imidazole-4-carboxamide 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: 77.0%

: 153887-20-8
5--1-imidazole-4-carboxamide

: 74-88-4
methyl iodide

: 153887-21-9
5-(1-benzoyl-2-methyl-3-isothioureido)-1-imidazole-4-carboxamide

Guidance literature:: With sodium hydroxide; for 1h;

Reference yield:

: 493-05-0
isochromane

: 153887-21-9
5-(1-benzoyl-2-methyl-3-isothioureido)-1-imidazole-4-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) HBr / 1) acetic acid, 4 h, reflux; 2) DMF, 2 h, reflux

2: 1.) hydrazine hydrate, 2.) hydrochloric acid / 1) ethanol, reflux, 10 min; 2) ethanol, reflux, 15 min

3: acetonitrile / 0.25 h / Heating

4: 92 percent / dimethylformamide / 1.5 h / Ambient temperature

5: 77 percent / aq. NaOH / 1 h

With hydrogenchloride; sodium hydroxide; hydrogen bromide; hydrazine hydrate; In N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 125593-25-1
o-(2-hydroxyethyl)benzylamine <2-ethanol>

: 153887-21-9
5-(1-benzoyl-2-methyl-3-isothioureido)-1-imidazole-4-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: acetonitrile / 0.25 h / Heating

2: 92 percent / dimethylformamide / 1.5 h / Ambient temperature

3: 77 percent / aq. NaOH / 1 h

With sodium hydroxide; In N,N-dimethyl-formamide; acetonitrile;