methyl (2S,5S)-4-oxo-2-(5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-5-ylcarbamate

Base Information

Chemical Name:methyl (2S,5S)-4-oxo-2-(5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-5-ylcarbamate
CAS No.:1399843-88-9
Molecular Formula:C₂₉H₃₃BN₄O₅
Molecular Weight:528.416
Hs Code.:

methyl (2S,5S)-4-oxo-2-(5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-5-ylcarbamate

Synonyms:methyl (2S,5S)-4-oxo-2-(5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-5-ylcarbamate

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Chemical Property of methyl (2S,5S)-4-oxo-2-(5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-5-ylcarbamate

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Technology Process of methyl (2S,5S)-4-oxo-2-(5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-5-ylcarbamate

There total 9 articles about methyl (2S,5S)-4-oxo-2-(5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-5-ylcarbamate 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: 97.0%

: 1399843-34-5
{(2S,5S)-2-[5-(4-bromo-phenyl)-1H-imidazol-2-yl]-4-oxo-1,2,4,5,6,7-hexahydro-azepino[3,2,1-hi]indol-5-yl}-carbamic acid methyl ester

: 73183-34-3
bis(pinacol)diborane

: 1399843-88-9
methyl (2S,5S)-4-oxo-2-(5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-5-ylcarbamate

Guidance literature:: With potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; at 110 ℃; Inert atmosphere; Sealed tube;

Reference yield: 79.7%

: 1399843-34-5
methyl (2S,5S)-2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-oxo-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-5-ylcarbamate

: 73183-34-3
bis(pinacol)diborane

: 1399843-88-9
methyl (2S,5S)-4-oxo-2-(4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-5-ylcarbamate

Guidance literature:: With potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; at 80 ℃; for 18h; Inert atmosphere;

Reference yield:

: 204326-24-9
(2S,11S)-11-([[(9H-fluoren-9-yl)methoxy]carbonyl]amino)-12-oxo-1-azatricyclo[6.4.1.0^[4,13]]trideca-4⁽¹³⁾,5,7-triene-2-carboxylic acid

: 1399843-88-9
methyl (2S,5S)-4-oxo-2-(5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-5-ylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1: piperidine / N,N-dimethyl-formamide / 1 h / 20 °C

2: sodium hydroxide; sodium carbonate / water / 3 h / 20 °C / Cooling with ice

3: N-ethyl-N,N-diisopropylamine / acetonitrile / 4 h / 20 °C

4: N-ethyl-N,N-diisopropylamine; ammonium acetate / xylene / 3 h / 140 °C / Inert atmosphere; Sealed tube

5: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 110 °C / Inert atmosphere; Sealed tube

With piperidine; ammonium acetate; potassium acetate; sodium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; water; N,N-dimethyl-formamide; acetonitrile; xylene;