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Butanamide, 4-[(6-chloro-1,2,3,5-tetrahydro-2-oxoimidazo[2,1-b]quinazolin-7-yl)oxy]- N-cyclohexyl-N-methyl-

Base Information Edit
  • Chemical Name:Butanamide, 4-[(6-chloro-1,2,3,5-tetrahydro-2-oxoimidazo[2,1-b]quinazolin-7-yl)oxy]- N-cyclohexyl-N-methyl-
  • CAS No.:105695-49-6
  • Molecular Formula:C21H27ClN4O3
  • Molecular Weight:418.923
  • Hs Code.:
  • Mol file:105695-49-6.mol
Butanamide,
4-[(6-chloro-1,2,3,5-tetrahydro-2-oxoimidazo[2,1-b]quinazolin-7-yl)oxy]-
N-cyclohexyl-N-methyl-

Synonyms:

Suppliers and Price of Butanamide, 4-[(6-chloro-1,2,3,5-tetrahydro-2-oxoimidazo[2,1-b]quinazolin-7-yl)oxy]- N-cyclohexyl-N-methyl-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of Butanamide, 4-[(6-chloro-1,2,3,5-tetrahydro-2-oxoimidazo[2,1-b]quinazolin-7-yl)oxy]- N-cyclohexyl-N-methyl- Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of Butanamide, 4-[(6-chloro-1,2,3,5-tetrahydro-2-oxoimidazo[2,1-b]quinazolin-7-yl)oxy]- N-cyclohexyl-N-methyl-

There total 10 articles about Butanamide, 4-[(6-chloro-1,2,3,5-tetrahydro-2-oxoimidazo[2,1-b]quinazolin-7-yl)oxy]- N-cyclohexyl-N-methyl- 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 5 steps
1: aq. NaCO3 / tetrahydrofuran / 1 h / Ambient temperature
2: 1.) AcONa / ethanol / 0.5 h
3: NaBH3CN / ethanol / 3 h
4: NiCl2*6H2O, NaBH4 / methanol
5: 2.) conc. aq. NH3 / 1.) EtOH, RT, overnight, 2.) EtOH
With ammonium hydroxide; sodium tetrahydroborate; sodium acetate; sodium cyanoborohydride; nickel dichloride; In tetrahydrofuran; methanol; ethanol;
DOI:10.1021/jm00385a012
Guidance literature:
Multi-step reaction with 8 steps
1: 38 g / K2CO3 / dimethylformamide
2: 82 percent / 2N HCl / dioxane / 2 h / Heating
3: oxalyl chloride / benzene; dimethylformamide / 0.5 h
4: aq. NaCO3 / tetrahydrofuran / 1 h / Ambient temperature
5: 1.) AcONa / ethanol / 0.5 h
6: NaBH3CN / ethanol / 3 h
7: NiCl2*6H2O, NaBH4 / methanol
8: 2.) conc. aq. NH3 / 1.) EtOH, RT, overnight, 2.) EtOH
With hydrogenchloride; ammonium hydroxide; sodium tetrahydroborate; oxalyl dichloride; sodium acetate; sodium cyanoborohydride; potassium carbonate; nickel dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00385a012
Guidance literature:
Multi-step reaction with 5 steps
1: aq. NaCO3 / tetrahydrofuran / 1 h / Ambient temperature
2: 1.) AcONa / ethanol / 0.5 h
3: NaBH3CN / ethanol / 3 h
4: NiCl2*6H2O, NaBH4 / methanol
5: 2.) conc. aq. NH3 / 1.) EtOH, RT, overnight, 2.) EtOH
With ammonium hydroxide; sodium tetrahydroborate; sodium acetate; sodium cyanoborohydride; nickel dichloride; In tetrahydrofuran; methanol; ethanol;
DOI:10.1021/jm00385a012
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