5-Bromo-1-(1-methylethyl)-2-[2-[4-(3-trifluoromethylphenyl)-1-piperazinyl]ethyl]-1H-naphth[1,2-d]imidazole

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Chemical Name:5-Bromo-1-(1-methylethyl)-2-[2-[4-(3-trifluoromethylphenyl)-1-piperazinyl]ethyl]-1H-naphth[1,2-d]imidazole
CAS No.:80429-29-4
Molecular Formula:C₂₇H₂₈BrF₃N₄
Molecular Weight:545.445
Hs Code.:

Synonyms:5-Bromo-1-(1-methylethyl)-2-[2-[4-(3-trifluoromethylphenyl)-1-piperazinyl]ethyl]-1H-naphth[1,2-d]imidazole

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Chemical Property of 5-Bromo-1-(1-methylethyl)-2-[2-[4-(3-trifluoromethylphenyl)-1-piperazinyl]ethyl]-1H-naphth[1,2-d]imidazole

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Technology Process of 5-Bromo-1-(1-methylethyl)-2-[2-[4-(3-trifluoromethylphenyl)-1-piperazinyl]ethyl]-1H-naphth[1,2-d]imidazole

There total 5 articles about 5-Bromo-1-(1-methylethyl)-2-[2-[4-(3-trifluoromethylphenyl)-1-piperazinyl]ethyl]-1H-naphth[1,2-d]imidazole 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:

: 5467-58-3
1-bromo-4-methoxynaphthalene

: 80429-29-4
5-Bromo-1-(1-methylethyl)-2-[2-[4-(3-trifluoromethylphenyl)-1-piperazinyl]ethyl]-1H-naphth[1,2-d]imidazole

Guidance literature:: Multi-step reaction with 4 steps

1: 49 percent / 99percent nitric acid, 96percent sulfuric acid / acetic anhydride / 0.17 h / -30 °C

2: 125 g / dimethylformamide / 1 h / Ambient temperature

3: 64 percent / 1,2-dichloro-ethane / 6 h / 120 °C

With sulfuric acid; nitric acid; In acetic anhydride; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/0223-5234(87)90053-5

Reference yield:

: 2216-69-5
1-Methoxynaphthalene

: 80429-29-4
5-Bromo-1-(1-methylethyl)-2-[2-[4-(3-trifluoromethylphenyl)-1-piperazinyl]ethyl]-1H-naphth[1,2-d]imidazole

Guidance literature:: Multi-step reaction with 5 steps

1: 91.5 percent / N-bromosuccinimide / CCl₄ / 4 h / Heating; Irradiation

2: 49 percent / 99percent nitric acid, 96percent sulfuric acid / acetic anhydride / 0.17 h / -30 °C

3: 125 g / dimethylformamide / 1 h / Ambient temperature

4: 64 percent / 1,2-dichloro-ethane / 6 h / 120 °C

With N-Bromosuccinimide; sulfuric acid; nitric acid; In tetrachloromethane; acetic anhydride; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/0223-5234(87)90053-5