5-<(N-benzoyl-S-methyl(isothiocarbamoyl))amino>-1-methylbenzimidazole-4-carbonitrile

Base Information

Chemical Name:5-<(N-benzoyl-S-methyl(isothiocarbamoyl))amino>-1-methylbenzimidazole-4-carbonitrile
CAS No.:103884-28-2
Molecular Formula:C₁₈H₁₅N₅OS
Molecular Weight:349.416
Hs Code.:

Synonyms:5-<(N-benzoyl-S-methyl(isothiocarbamoyl))amino>-1-methylbenzimidazole-4-carbonitrile

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Chemical Property of 5-<(N-benzoyl-S-methyl(isothiocarbamoyl))amino>-1-methylbenzimidazole-4-carbonitrile

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Technology Process of 5-<(N-benzoyl-S-methyl(isothiocarbamoyl))amino>-1-methylbenzimidazole-4-carbonitrile

There total 4 articles about 5-<(N-benzoyl-S-methyl(isothiocarbamoyl))amino>-1-methylbenzimidazole-4-carbonitrile 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:

: 2044-88-4
N-methyl-2,4-dinitroaniline

: 103884-28-2
5-<(N-benzoyl-S-methyl(isothiocarbamoyl))amino>-1-methylbenzimidazole-4-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: 43 percent / potassium ferricyanide / methanol; H₂O / 6 h / 55 °C

2: 1.) H₂ / 1.) 10percent Pd/C / 1.) EtOH, 52 psi, reflux, 2 h, 2.) reflux, 2 h

3: 98.6 percent / H₂O / 24 h / Ambient temperature

4: NaOH / H₂O / 24 h

With sodium hydroxide; hydrogen; potassium hexacyanoferrate(III); palladium on activated charcoal; In methanol; water;
DOI:10.1021/jo00371a029

Reference yield:

: 103884-25-9
3-(methylamino)-2,6-dinitrobenzonitrile

: 103884-28-2
5-<(N-benzoyl-S-methyl(isothiocarbamoyl))amino>-1-methylbenzimidazole-4-carbonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) H₂ / 1.) 10percent Pd/C / 1.) EtOH, 52 psi, reflux, 2 h, 2.) reflux, 2 h

2: 98.6 percent / H₂O / 24 h / Ambient temperature

3: NaOH / H₂O / 24 h

With sodium hydroxide; hydrogen; palladium on activated charcoal; In water;
DOI:10.1021/jo00371a029

Reference yield:

: 103884-26-0
5-amino-1-methylbenzimidazole-4-carbonitrile

: 103884-28-2
5-<(N-benzoyl-S-methyl(isothiocarbamoyl))amino>-1-methylbenzimidazole-4-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 98.6 percent / H₂O / 24 h / Ambient temperature

2: NaOH / H₂O / 24 h

With sodium hydroxide; In water;
DOI:10.1021/jo00371a029