5-(2-aminophenyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazole-4-carbonitrile

Base Information

Chemical Name:5-(2-aminophenyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazole-4-carbonitrile
CAS No.:1375262-91-1
Molecular Formula:C₁₄H₁₆N₄O
Molecular Weight:256.307
Hs Code.:

Synonyms:5-(2-aminophenyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazole-4-carbonitrile

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-(2-aminophenyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazole-4-carbonitrile

Chemical Property:

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Safty Information:

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MSDS Files:: SDS file from LookChem

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Technology Process of 5-(2-aminophenyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazole-4-carbonitrile

There total 2 articles about 5-(2-aminophenyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazole-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: 89.0%

: 2-amino-benzeneboronic acid hydrochloride

: 1375262-95-5
1-(2-hydroxy-2-methylpropyl)-5-iodo-1H-imidazole-4-carbonitrile

: 1375262-91-1
5-(2-aminophenyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazole-4-carbonitrile

Guidance literature:: With palladium diacetate; sodium carbonate; triphenylphosphine; In 1,2-dimethoxyethane; water; at 100 ℃; for 3h; Inert atmosphere;
DOI:10.1021/ml300079e

Reference yield:

: 1375262-89-7
5-amino-1-(2-hydroxy-2-methylpropyl)-1H-imidazole-4-carbonitrile

: 1375262-91-1
5-(2-aminophenyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazole-4-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: diiodomethane; isopentyl nitrite / chloroform / 0.83 h / 80 °C / Inert atmosphere

2: palladium diacetate; sodium carbonate; triphenylphosphine / 1,2-dimethoxyethane; water / 3 h / 100 °C / Inert atmosphere

With diiodomethane; palladium diacetate; sodium carbonate; triphenylphosphine; isopentyl nitrite; In 1,2-dimethoxyethane; chloroform; water; 1: Sandmeyer reaction / 2: Suzuki coupling;
DOI:10.1021/ml300079e