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N-{3-[7-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]propyl}propanamide monoformate

Base Information
  • Chemical Name:N-{3-[7-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]propyl}propanamide monoformate
  • CAS No.:1258853-30-3
  • Molecular Formula:CH2O2*C28H33N5O3
  • Molecular Weight:533.627
  • Hs Code.:
N-{3-[7-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]propyl}propanamide monoformate

Synonyms:N-{3-[7-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]propyl}propanamide monoformate

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Chemical Property of N-{3-[7-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]propyl}propanamide monoformate
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Technology Process of N-{3-[7-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]propyl}propanamide monoformate

There total 11 articles about N-{3-[7-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]propyl}propanamide monoformate 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:
5-{3-[3-(3-aminopropyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1,2,4-oxadiazol-5-yl}-2-[(1-methylethyl)oxy]benzonitrile monohydrochloride; propionyl chloride; With pyridine; In dichloromethane; at 20 ℃; for 0.333333h;
formic acid;
Guidance literature:
Multi-step reaction with 8 steps
1: oxalyl dichloride / N,N-dimethyl-formamide / 4 h / 20 °C
2: pyridine / toluene / 1.5 h / 110 °C / Inert atmosphere; Reflux
3: hydrogenchloride / dichloromethane; 1,4-dioxane; diethyl ether / 3.5 h
4: potassium carbonate / N,N-dimethyl-formamide / 4 h / 90 °C
5: sodium hydroxide / ethanol / 2 h / 20 °C
6: triethylamine; diphenylphosphoranyl azide / toluene / 2 h / 80 °C
7: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C
8: pyridine / dichloromethane / 0.33 h / 20 °C
With pyridine; hydrogenchloride; oxalyl dichloride; diphenylphosphoranyl azide; potassium carbonate; triethylamine; sodium hydroxide; N,N-dimethyl-formamide; In 1,4-dioxane; diethyl ether; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;
Guidance literature:
Multi-step reaction with 9 steps
1: tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 1.25 h / 100 °C / Inert atmosphere
2: hydroxylamine hydrochloride; sodium hydrogencarbonate / ethanol / 4 h / 60 °C / Reflux
3: pyridine / toluene / 1.5 h / 110 °C / Inert atmosphere; Reflux
4: hydrogenchloride / dichloromethane; 1,4-dioxane; diethyl ether / 3.5 h
5: potassium carbonate / N,N-dimethyl-formamide / 4 h / 90 °C
6: sodium hydroxide / ethanol / 2 h / 20 °C
7: triethylamine; diphenylphosphoranyl azide / toluene / 2 h / 80 °C
8: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C
9: pyridine / dichloromethane / 0.33 h / 20 °C
With pyridine; hydrogenchloride; diphenylphosphoranyl azide; hydroxylamine hydrochloride; sodium hydrogencarbonate; potassium carbonate; triethylamine; sodium hydroxide; tetrakis(triphenylphosphine) palladium(0); In 1,4-dioxane; diethyl ether; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;
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