2-[3'-fluoro-4'-(N-hydroxyamidino)biphenyl-4-yl]-1H-benzimidazole-5-(N-hydroxy)amidine

Base Information

Chemical Name:2-[3'-fluoro-4'-(N-hydroxyamidino)biphenyl-4-yl]-1H-benzimidazole-5-(N-hydroxy)amidine
CAS No.:869767-82-8
Molecular Formula:C₂₁H₁₇FN₆O₂
Molecular Weight:404.403
Hs Code.:

Synonyms:2-[3'-fluoro-4'-(N-hydroxyamidino)biphenyl-4-yl]-1H-benzimidazole-5-(N-hydroxy)amidine

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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 2-[3'-fluoro-4'-(N-hydroxyamidino)biphenyl-4-yl]-1H-benzimidazole-5-(N-hydroxy)amidine

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Technology Process of 2-[3'-fluoro-4'-(N-hydroxyamidino)biphenyl-4-yl]-1H-benzimidazole-5-(N-hydroxy)amidine

There total 5 articles about 2-[3'-fluoro-4'-(N-hydroxyamidino)biphenyl-4-yl]-1H-benzimidazole-5-(N-hydroxy)amidine 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: 96.0%

: 851340-78-8
2-(4'-cyano-3'-fluorobiphenyl-4-yl)-1H-benzimidazole-5-carbonitrile

: 869767-82-8
2-[3'-fluoro-4'-(N-hydroxyamidino)biphenyl-4-yl]-1H-benzimidazole-5-(N-hydroxy)amidine

Guidance literature:: With hydroxylamine hydrochloride; potassium tert-butylate; In dimethyl sulfoxide; at 20 ℃;
DOI:10.1016/j.bmc.2005.07.024

Reference yield: 96.0%

: 869767-82-8
2-[3'-fluoro-4'-(N-hydroxyamidino)biphenyl-4-yl]-1H-benzimidazole-5-(N-hydroxy)amidine

Guidance literature:

Reference yield:

: 87199-17-5
4-formylphenylboronic acid,

: 869767-82-8
2-[3'-fluoro-4'-(N-hydroxyamidino)biphenyl-4-yl]-1H-benzimidazole-5-(N-hydroxy)amidine

Guidance literature:: Multi-step reaction with 3 steps

1: 78 percent / Na₂CO₃ / tetrakis(triphenylphosphine)palladium / toluene; H₂O; methanol / 12 h / 80 °C

2: 84 percent / sodium hydrogen sulfite / dimethylformamide / Heating

3: 96 percent / hydroxylamine hydrochloride; potassium t-butoxide / dimethylsulfoxide / 20 °C

With hydroxylamine hydrochloride; potassium tert-butylate; sodium carbonate; sodium hydrogensulfite; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In methanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene; 1: Suzuki coupling;
DOI:10.1016/j.bmc.2005.07.024