N-1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazol-4-methyl-acetamide

Base Information

Chemical Name:N-1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazol-4-methyl-acetamide
CAS No.:327619-55-6
Molecular Formula:C₂₃H₁₇F₄N₃O
Molecular Weight:427.401
Hs Code.:

Synonyms:N-1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazol-4-methyl-acetamide

Suppliers and Price of N-1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazol-4-methyl-acetamide

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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 N-1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazol-4-methyl-acetamide

Chemical Property:

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Technology Process of N-1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazol-4-methyl-acetamide

There total 9 articles about N-1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazol-4-methyl-acetamide 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: 65.0%

: 108-24-7
acetic anhydride

: 407629-69-0
1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazol-4-yl-methylamine

: 327619-55-6
N-1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazol-4-methyl-acetamide

Guidance literature:: With triethylamine; In tetrahydrofuran; at 20 ℃; for 1.5h;
DOI:10.1021/jm060103d

Reference yield:

: 212503-82-7
methyl N,N-bis(2,6-difluorobenzoyl)-3-nitro-2-anilinecarboxylate

: 327619-55-6
N-1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazol-4-methyl-acetamide

Guidance literature:: Multi-step reaction with 10 steps

1: 92 percent / pyridine; NH₂NH₂ / 6 h / 20 °C

2: 60 percent / LiAlH₄ / tetrahydrofuran / 4 h / 0 - 20 °C

3: 75 percent / Et₃N / tetrahydrofuran / 20 °C

4: 75 percent / Fe; AcOH / 0.5 h / Heating

5: 76 percent / NaH / tetrahydrofuran / 6 h

6: 96 percent / K₂CO₃ / methanol; H₂O / 0.5 h

7: 92 percent / SOCl₂ / CHCl₃ / 3 h / 20 °C

8: 93 percent / NaN₃ / dimethylformamide / 1 h / 20 °C

9: 31 percent / Zn; AcOH / 1 h / 20 °C

10: 65 percent / Et₃N / tetrahydrofuran / 1.5 h / 20 °C

With pyridine; lithium aluminium tetrahydride; thionyl chloride; sodium azide; iron; sodium hydride; potassium carbonate; acetic acid; triethylamine; hydrazine; zinc; In tetrahydrofuran; methanol; chloroform; water; N,N-dimethyl-formamide;
DOI:10.1021/jm060103d

Reference yield:

: 327619-43-2
2,6-difluorobenzoic acid 2-hydroxymethyl-6-nitroanilide

: 327619-55-6
N-1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazol-4-methyl-acetamide

Guidance literature:: Multi-step reaction with 8 steps

1: 75 percent / Et₃N / tetrahydrofuran / 20 °C

2: 75 percent / Fe; AcOH / 0.5 h / Heating

3: 76 percent / NaH / tetrahydrofuran / 6 h

4: 96 percent / K₂CO₃ / methanol; H₂O / 0.5 h

5: 92 percent / SOCl₂ / CHCl₃ / 3 h / 20 °C

6: 93 percent / NaN₃ / dimethylformamide / 1 h / 20 °C

7: 31 percent / Zn; AcOH / 1 h / 20 °C

8: 65 percent / Et₃N / tetrahydrofuran / 1.5 h / 20 °C

With thionyl chloride; sodium azide; iron; sodium hydride; potassium carbonate; acetic acid; triethylamine; zinc; In tetrahydrofuran; methanol; chloroform; water; N,N-dimethyl-formamide;
DOI:10.1021/jm060103d