3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid[1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-yl]amide

Base Information

Chemical Name:3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid[1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-yl]amide
CAS No.:1426409-09-7
Molecular Formula:C₃₃H₃₄N₄O₄
Molecular Weight:550.657
Hs Code.:

Synonyms:3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid[1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-yl]amide

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Chemical Property of 3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid[1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-yl]amide

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Technology Process of 3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid[1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-yl]amide

There total 9 articles about 3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid[1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-yl]amide 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:

: 1426408-60-7
1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-ylamine

: 1426409-08-6
3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid

: 1426409-09-7
3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid[1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-yl]amide

Guidance literature:: 1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-ylamine; 3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid; With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃; for 14h;

With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 72h;

Reference yield:

: 1426408-59-4
1-phenyl-5-(3-propylphenyl)-4,5-dihydro-1H-pyrazol-3-ylamine

: 1426409-09-7
3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid[1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-yl]amide

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyrographite; oxygen / toluene / pH 5 - 8 / Reflux

2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 14 h / 20 °C

2.2: 72 h / 20 °C

With oxygen; pyrographite; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; toluene;

Reference yield:

: 1426409-04-2
N-[2-(tert-butyldimethylsilanyloxymethyl)allyl]-2-diazo-N-(2,4-dimethoxybenzyl)acetamide

: 1426409-09-7
3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid[1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-yl]amide

Guidance literature:: Multi-step reaction with 5 steps

1.1: rhodium(II) acetate dimer; α,α,α-trifluorotoluene / 24 h / 50 °C / Inert atmosphere

2.1: tetranormalbutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C

3.1: triethylamine; sulfur trioxide pyridine complex / chloroform; dimethyl sulfoxide / 2 h / 20 °C / Inert atmosphere

4.1: sodium dihydrogenphosphate dihydrate; sodium chlorite / tetrahydrofuran; water; tert-butyl alcohol / 24 h / 0 - 20 °C / Inert atmosphere

5.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 14 h / 20 °C

5.2: 72 h / 20 °C

With tetranormalbutyl ammonium fluoride; sodium chlorite; sodium dihydrogenphosphate dihydrate; α,α,α-trifluorotoluene; rhodium(II) acetate dimer; sulfur trioxide pyridine complex; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; chloroform; water; dimethyl sulfoxide; N,N-dimethyl-formamide; tert-butyl alcohol;