{(2S,5S)-2-[5-(4-Bromo-2-fluoro-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

Base Information

Chemical Name:{(2S,5S)-2-[5-(4-Bromo-2-fluoro-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
CAS No.:1399844-99-5
Molecular Formula:C₂₃H₂₀BrFN₄O₃
Molecular Weight:499.339
Hs Code.:

Synonyms:{(2S,5S)-2-[5-(4-Bromo-2-fluoro-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

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Chemical Property of {(2S,5S)-2-[5-(4-Bromo-2-fluoro-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

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Technology Process of {(2S,5S)-2-[5-(4-Bromo-2-fluoro-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

There total 4 articles about {(2S,5S)-2-[5-(4-Bromo-2-fluoro-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 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: 80.0%

: 1399844-98-4
(2S,5S)-5-methoxycarbonylamino-4-oxo-1,2,4,5,6,7-hexahydro-azepino[3,2,1-hi]indole-2-carboxylic acid 2-(4-bromo-2-fluoro-phenyl)-2-oxo-ethylester

: 1399844-99-5
{(2S,5S)-2-[5-(4-Bromo-2-fluoro-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

Guidance literature:: With ammonium acetate; In xylene; at 140 ℃; for 3h; Inert atmosphere; Sealed tube;

Reference yield:

: 5-(S)-amino-1,2,4,5,6,7-hexahydro-azepino <3,2,1-hi> indole-4-one-2-(S)-carboxylic acid

: 1399844-99-5
{(2S,5S)-2-[5-(4-Bromo-2-fluoro-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

Guidance literature:: Multi-step reaction with 3 steps

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

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

3: ammonium acetate / xylene / 3 h / 140 °C / Inert atmosphere; Sealed tube

With ammonium acetate; sodium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In water; acetonitrile; xylene;

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

: 1399844-99-5
{(2S,5S)-2-[5-(4-Bromo-2-fluoro-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

Guidance literature:: Multi-step reaction with 4 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: ammonium acetate / xylene / 3 h / 140 °C / Inert atmosphere; Sealed tube

With piperidine; ammonium acetate; sodium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In water; N,N-dimethyl-formamide; acetonitrile; xylene;