N-(6-{4-[3-(2-fluoro-5-trifluoromethyl-phenyl)-ureido]-phenoxy}-1H-benzoimidazol-2-yl)-2-(4-methyl-piperazin-1-yl)-acetamide

Base Information

Chemical Name:N-(6-{4-[3-(2-fluoro-5-trifluoromethyl-phenyl)-ureido]-phenoxy}-1H-benzoimidazol-2-yl)-2-(4-methyl-piperazin-1-yl)-acetamide
CAS No.:433225-03-7
Molecular Formula:C₂₈H₂₇F₄N₇O₃
Molecular Weight:585.561
Hs Code.:

Synonyms:N-(6-{4-[3-(2-fluoro-5-trifluoromethyl-phenyl)-ureido]-phenoxy}-1H-benzoimidazol-2-yl)-2-(4-methyl-piperazin-1-yl)-acetamide

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Chemical Property of N-(6-{4-[3-(2-fluoro-5-trifluoromethyl-phenyl)-ureido]-phenoxy}-1H-benzoimidazol-2-yl)-2-(4-methyl-piperazin-1-yl)-acetamide

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Technology Process of N-(6-{4-[3-(2-fluoro-5-trifluoromethyl-phenyl)-ureido]-phenoxy}-1H-benzoimidazol-2-yl)-2-(4-methyl-piperazin-1-yl)-acetamide

There total 5 articles about N-(6-{4-[3-(2-fluoro-5-trifluoromethyl-phenyl)-ureido]-phenoxy}-1H-benzoimidazol-2-yl)-2-(4-methyl-piperazin-1-yl)-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: 50.0%

: 433224-24-9
C₂₁H₁₅F₄N₅O₂

: 54699-92-2
(4-Methyl-piperazin-1-yl)-acetic acid

: 433225-03-7
N-(6-{4-[3-(2-fluoro-5-trifluoromethyl-phenyl)-ureido]-phenoxy}-1H-benzoimidazol-2-yl)-2-(4-methyl-piperazin-1-yl)-acetamide

Guidance literature:: With benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In N,N-dimethyl-formamide; for 4h;
DOI:10.1021/jm0611051

Reference yield:

: 1635-61-6
5-chloro-2-nitroaniline

: 433225-03-7
N-(6-{4-[3-(2-fluoro-5-trifluoromethyl-phenyl)-ureido]-phenoxy}-1H-benzoimidazol-2-yl)-2-(4-methyl-piperazin-1-yl)-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: NaH / dimethylformamide / 90 °C

2: 21.6 g / tetrahydrofuran / 20 °C

3: 13.0 g / H₂ / Pd/C / ethanol / 72 h

4: 96 percent / methanol / 1 h

5: 50 percent / Et₃N; HBTU; HOBT / dimethylformamide / 4 h

With hydrogen; sodium hydride; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm0611051

Reference yield:

: 30491-74-8
3,4'-diamino-4-nitrodiphenyl ether

: 433225-03-7
N-(6-{4-[3-(2-fluoro-5-trifluoromethyl-phenyl)-ureido]-phenoxy}-1H-benzoimidazol-2-yl)-2-(4-methyl-piperazin-1-yl)-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 21.6 g / tetrahydrofuran / 20 °C

2: 13.0 g / H₂ / Pd/C / ethanol / 72 h

3: 96 percent / methanol / 1 h

4: 50 percent / Et₃N; HBTU; HOBT / dimethylformamide / 4 h

With hydrogen; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm0611051