1,1-dimethylethyl 7-{3-[(difluoromethyl)oxy]-4-(methyloxy)phenyl}-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate

Base Information

Chemical Name:1,1-dimethylethyl 7-{3-[(difluoromethyl)oxy]-4-(methyloxy)phenyl}-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate
CAS No.:1379596-59-4
Molecular Formula:C₂₂H₂₅F₂NO₅
Molecular Weight:421.441
Hs Code.:

Synonyms:1,1-dimethylethyl 7-{3-[(difluoromethyl)oxy]-4-(methyloxy)phenyl}-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate

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Chemical Property of 1,1-dimethylethyl 7-{3-[(difluoromethyl)oxy]-4-(methyloxy)phenyl}-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate

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Technology Process of 1,1-dimethylethyl 7-{3-[(difluoromethyl)oxy]-4-(methyloxy)phenyl}-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate

There total 5 articles about 1,1-dimethylethyl 7-{3-[(difluoromethyl)oxy]-4-(methyloxy)phenyl}-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate 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: 58.0%

: 1251164-95-0
tert-butyl 7-dihydroxyboryl-2,3-dihydro-5H-benzo[f ]-[1,4]-oxazepine-4(5H)-carboxylate

: 1261818-69-2
4-bromo-2-[(difluoromethyl)oxy]-1-(methyloxy)benzene

: 1379596-59-4
1,1-dimethylethyl 7-{3-[(difluoromethyl)oxy]-4-(methyloxy)phenyl}-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate

Guidance literature:: With potassium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; water; at 110 ℃; for 0.283333h; Inert atmosphere; Microwave irradiation;

Reference yield:

: 1217862-54-8
tert-butyl N-(5-bromo-2-hydroxybenzyl)-N-(2-hydroxyethyl)carbamate

: 1379596-59-4
1,1-dimethylethyl 7-{3-[(difluoromethyl)oxy]-4-(methyloxy)phenyl}-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: triphenylphosphine; di-isopropyl azodicarboxylate / dichloromethane / 12 h / 20 °C / Inert atmosphere

2.1: n-butyllithium / tetrahydrofuran / 1.17 h / -78 °C / Inert atmosphere

2.2: -78 - 20 °C

3.1: potassium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 0.28 h / 110 °C / Inert atmosphere; Microwave irradiation

With n-butyllithium; di-isopropyl azodicarboxylate; potassium carbonate; triphenylphosphine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1379596-59-4
1,1-dimethylethyl 7-{3-[(difluoromethyl)oxy]-4-(methyloxy)phenyl}-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium tetrahydroborate / tetrahydrofuran; methanol / 4 h / 40 °C / Inert atmosphere

1.2: 20 °C / Inert atmosphere

2.1: triphenylphosphine; di-isopropyl azodicarboxylate / dichloromethane / 12 h / 20 °C / Inert atmosphere

3.1: n-butyllithium / tetrahydrofuran / 1.17 h / -78 °C / Inert atmosphere

3.2: -78 - 20 °C

4.1: potassium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 0.28 h / 110 °C / Inert atmosphere; Microwave irradiation

With sodium tetrahydroborate; n-butyllithium; di-isopropyl azodicarboxylate; potassium carbonate; triphenylphosphine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water;