N-cyclohexyl-N-isopropyl-4-(2-oxo-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-7-yl)oxybutyramide

Base Information

Chemical Name:N-cyclohexyl-N-isopropyl-4-(2-oxo-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-7-yl)oxybutyramide
CAS No.:94192-75-3
Molecular Formula:C₂₃H₃₂N₄O₃
Molecular Weight:412.532
Hs Code.:

Synonyms:N-cyclohexyl-N-isopropyl-4-(2-oxo-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-7-yl)oxybutyramide

Suppliers and Price of N-cyclohexyl-N-isopropyl-4-(2-oxo-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-7-yl)oxybutyramide

Supply Marketing:

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 0 raw suppliers

Chemical Property of N-cyclohexyl-N-isopropyl-4-(2-oxo-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-7-yl)oxybutyramide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-cyclohexyl-N-isopropyl-4-(2-oxo-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-7-yl)oxybutyramide

There total 7 articles about N-cyclohexyl-N-isopropyl-4-(2-oxo-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-7-yl)oxybutyramide 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:

: 5459-93-8
N-ethyl-cyclohexanamine

: 94192-75-3
N-cyclohexyl-N-isopropyl-4-(2-oxo-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-7-yl)oxybutyramide

Guidance literature:: Multi-step reaction with 5 steps

1: aq. Na₂CO₃ / tetrahydrofuran / 1 h / Ambient temperature

2: 1.) AcONa / ethanol / 0.5 h

3: NaBH₃Cn / ethanol / 3 h

4: H₂ / 10percent Pd/C / ethanol

5: 2.) conc. aq. NH₃ / 1.) EtOH, RT, overnight, 2.) EtOH, RT, 30 min

With ammonium hydroxide; hydrogen; sodium acetate; sodium cyanoborohydride; sodium carbonate; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00385a012

Reference yield:

: 105695-09-8
N-Cyclohexyl-N-ethyl-4-(3-formyl-4-nitro-phenoxy)-butyramide

: 94192-75-3
N-cyclohexyl-N-isopropyl-4-(2-oxo-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-7-yl)oxybutyramide

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) AcONa / ethanol / 0.5 h

2: NaBH₃Cn / ethanol / 3 h

3: H₂ / 10percent Pd/C / ethanol

4: 2.) conc. aq. NH₃ / 1.) EtOH, RT, overnight, 2.) EtOH, RT, 30 min

With ammonium hydroxide; hydrogen; sodium acetate; sodium cyanoborohydride; palladium on activated charcoal; In ethanol;
DOI:10.1021/jm00385a012

Reference yield:

: {5-[3-(Cyclohexyl-ethyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

: 94192-75-3
N-cyclohexyl-N-isopropyl-4-(2-oxo-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-7-yl)oxybutyramide

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 10percent Pd/C / ethanol

2: 2.) conc. aq. NH₃ / 1.) EtOH, RT, overnight, 2.) EtOH, RT, 30 min

With ammonium hydroxide; hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1021/jm00385a012