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((S)-1-{(2S,5S)-2-[5-(4-bromo-phenyl)-1H-imidazol-2-yl]-5-methyl-piperidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester

Base Information
  • Chemical Name:((S)-1-{(2S,5S)-2-[5-(4-bromo-phenyl)-1H-imidazol-2-yl]-5-methyl-piperidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
  • CAS No.:1476720-95-2
  • Molecular Formula:C22H29BrN4O3
  • Molecular Weight:477.401
  • Hs Code.:
((S)-1-{(2S,5S)-2-[5-(4-bromo-phenyl)-1H-imidazol-2-yl]-5-methyl-piperidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester

Synonyms:((S)-1-{(2S,5S)-2-[5-(4-bromo-phenyl)-1H-imidazol-2-yl]-5-methyl-piperidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester

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Chemical Property of ((S)-1-{(2S,5S)-2-[5-(4-bromo-phenyl)-1H-imidazol-2-yl]-5-methyl-piperidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
Chemical Property:
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Technology Process of ((S)-1-{(2S,5S)-2-[5-(4-bromo-phenyl)-1H-imidazol-2-yl]-5-methyl-piperidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester

There total 11 articles about ((S)-1-{(2S,5S)-2-[5-(4-bromo-phenyl)-1H-imidazol-2-yl]-5-methyl-piperidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester 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:
Guidance literature:
Multi-step reaction with 2 steps
1: sodium carbonate; sodium hydroxide / water / 0 - 20 °C / Inert atmosphere
2: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 20 °C / Inert atmosphere
With sodium carbonate; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; In dichloromethane; water;
Guidance literature:
Multi-step reaction with 10 steps
1.1: water; acetic acid / 3 h / Inert atmosphere; Reflux
2.1: thionyl chloride / 0 - 20 °C / Inert atmosphere
3.1: dmap / acetonitrile / 0 - 20 °C / Inert atmosphere
4.1: lithium hexamethyldisilazane / tetrahydrofuran; toluene / 1 h / -78 °C / Inert atmosphere
4.2: -78 °C / Inert atmosphere
5.1: dimethylsulfide borane complex / tetrahydrofuran / 0 - 40 °C / Inert atmosphere
6.1: water; lithium hydroxide monohydrate / methanol / 20 °C / Inert atmosphere
7.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 20 °C / Inert atmosphere
8.1: ammonium acetate / toluene / Inert atmosphere; Reflux
9.1: hydrogenchloride / 1,4-dioxane / 3 h / 20 °C / Inert atmosphere
10.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 20 °C / Inert atmosphere
With hydrogenchloride; dmap; thionyl chloride; lithium hydroxide monohydrate; dimethylsulfide borane complex; ammonium acetate; water; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; toluene; acetonitrile;
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