1-benzyl-3-diisopropoxyphosphoryloxy-4-methylene-3-phenyl-3,4-dihydro-2-quinolone

Base Information

Chemical Name:1-benzyl-3-diisopropoxyphosphoryloxy-4-methylene-3-phenyl-3,4-dihydro-2-quinolone
CAS No.:1615653-09-2
Molecular Formula:C₂₉H₃₂NO₅P
Molecular Weight:505.551
Hs Code.:

Synonyms:1-benzyl-3-diisopropoxyphosphoryloxy-4-methylene-3-phenyl-3,4-dihydro-2-quinolone

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Chemical Property of 1-benzyl-3-diisopropoxyphosphoryloxy-4-methylene-3-phenyl-3,4-dihydro-2-quinolone

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Technology Process of 1-benzyl-3-diisopropoxyphosphoryloxy-4-methylene-3-phenyl-3,4-dihydro-2-quinolone

There total 4 articles about 1-benzyl-3-diisopropoxyphosphoryloxy-4-methylene-3-phenyl-3,4-dihydro-2-quinolone 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: 88.0%

: 1809-20-7
diisopropyl hydrogenphosphonate

: 1615652-88-4
N-benzyl-N-(2-ethynylphenyl)-2-oxo-2-phenylacetamide

: 1615653-09-2
1-benzyl-3-diisopropoxyphosphoryloxy-4-methylene-3-phenyl-3,4-dihydro-2-quinolone

Guidance literature:: With 1-tert-butyl-2,2,4,4,4-pentakis(dimethylamino)-2Λ⁵,4Λ⁵-catenadi(phosphazene); In tetrahydrofuran; dimethyl sulfoxide; at 20 ℃; for 4h; Inert atmosphere;
DOI:10.1021/ol501479t

Reference yield:

: 324738-51-4
2′-N-benzylaminophenylacetylene

: 1615653-09-2
1-benzyl-3-diisopropoxyphosphoryloxy-4-methylene-3-phenyl-3,4-dihydro-2-quinolone

Guidance literature:: Multi-step reaction with 2 steps

1.1: Dichloromethyl methyl ether / dichloromethane / 1 h / 20 °C / Inert atmosphere

1.2: 24 h / 0 - 20 °C / Inert atmosphere

2.1: 1-tert-butyl-2,2,4,4,4-pentakis(dimethylamino)-2Λ⁵,4Λ⁵-catenadi(phosphazene) / tetrahydrofuran; dimethyl sulfoxide / 4 h / 20 °C / Inert atmosphere

With Dichloromethyl methyl ether; 1-tert-butyl-2,2,4,4,4-pentakis(dimethylamino)-2Λ⁵,4Λ⁵-catenadi(phosphazene); In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;
DOI:10.1021/ol501479t

Reference yield:

: 76464-99-8
N-benzyl-2-iodoaniline

: 1615653-09-2
1-benzyl-3-diisopropoxyphosphoryloxy-4-methylene-3-phenyl-3,4-dihydro-2-quinolone

Guidance literature:: Multi-step reaction with 3 steps

1.1: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / N,N-dimethyl-formamide; triethylamine / 18 h / 20 °C / Inert atmosphere

2.1: Dichloromethyl methyl ether / dichloromethane / 1 h / 20 °C / Inert atmosphere

2.2: 24 h / 0 - 20 °C / Inert atmosphere

3.1: 1-tert-butyl-2,2,4,4,4-pentakis(dimethylamino)-2Λ⁵,4Λ⁵-catenadi(phosphazene) / tetrahydrofuran; dimethyl sulfoxide / 4 h / 20 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; Dichloromethyl methyl ether; 1-tert-butyl-2,2,4,4,4-pentakis(dimethylamino)-2Λ⁵,4Λ⁵-catenadi(phosphazene); In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; triethylamine; N,N-dimethyl-formamide;
DOI:10.1021/ol501479t