6-{1-[4-(benzyloxy)butyl]-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-yl}-2H-1,4-benzoxazin-3(4H)-one

Base Information

Chemical Name:6-{1-[4-(benzyloxy)butyl]-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-yl}-2H-1,4-benzoxazin-3(4H)-one
CAS No.:1221503-12-3
Molecular Formula:C₂₉H₂₈FN₃O₃
Molecular Weight:485.558
Hs Code.:

Synonyms:6-{1-[4-(benzyloxy)butyl]-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-yl}-2H-1,4-benzoxazin-3(4H)-one

Suppliers and Price of 6-{1-[4-(benzyloxy)butyl]-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-yl}-2H-1,4-benzoxazin-3(4H)-one

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 6-{1-[4-(benzyloxy)butyl]-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-yl}-2H-1,4-benzoxazin-3(4H)-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-{1-[4-(benzyloxy)butyl]-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-yl}-2H-1,4-benzoxazin-3(4H)-one

There total 7 articles about 6-{1-[4-(benzyloxy)butyl]-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-yl}-2H-1,4-benzoxazin-3(4H)-one 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: 44.0%

: 943994-02-3
6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-benzo[b][1,4]oxazin-3(4H)-one

: 1221503-11-2
1-[4-(benzyloxy)butyl]-4-bromo-5-(4-fluorophenyl)-3-methyl-1H-pyrazole

: 1221503-12-3
6-{1-[4-(benzyloxy)butyl]-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-yl}-2H-1,4-benzoxazin-3(4H)-one

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; caesium carbonate; In tetrahydrofuran; water; for 18h; Inert atmosphere; Reflux;
DOI:10.1016/j.bmc.2014.07.038

Reference yield:

: 50873-93-3
[(4-chlorobutoxy)methyl]benzene

: 1221503-12-3
6-{1-[4-(benzyloxy)butyl]-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-yl}-2H-1,4-benzoxazin-3(4H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: hydrazine hydrate; sodium hydroxide / 2 h / 95 °C

2: triethylamine; trifluoroacetic acid / isopropyl alcohol / 1 h / 80 °C

3: N-Bromosuccinimide / acetonitrile / 0.17 h / 20 °C

4: caesium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / tetrahydrofuran; water / 18 h / Inert atmosphere; Reflux

With N-Bromosuccinimide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; caesium carbonate; hydrazine hydrate; triethylamine; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; water; isopropyl alcohol; acetonitrile; 4: |Suzuki Coupling;
DOI:10.1016/j.bmc.2014.07.038

Reference yield:

: 403-42-9
1-(4-fluorophenyl)ethanone

: 1221503-12-3
6-{1-[4-(benzyloxy)butyl]-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-yl}-2H-1,4-benzoxazin-3(4H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran / 0.5 h / 20 °C

1.2: 3 h / 40 °C

2.1: triethylamine; trifluoroacetic acid / isopropyl alcohol / 1 h / 80 °C

3.1: N-Bromosuccinimide / acetonitrile / 0.17 h / 20 °C

4.1: caesium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / tetrahydrofuran; water / 18 h / Inert atmosphere; Reflux

With N-Bromosuccinimide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; sodium hydride; caesium carbonate; triethylamine; trifluoroacetic acid; In tetrahydrofuran; water; isopropyl alcohol; acetonitrile; 4.1: |Suzuki Coupling;
DOI:10.1016/j.bmc.2014.07.038