5-amino-4-(((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)amino)-2-fluorobenzonitrile

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Chemical Name:5-amino-4-(((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)amino)-2-fluorobenzonitrile
CAS No.:1437790-15-2
Molecular Formula:C₂₄H₂₇FN₄O₂
Molecular Weight:422.502
Hs Code.:

Synonyms:5-amino-4-(((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)amino)-2-fluorobenzonitrile

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Chemical Property of 5-amino-4-(((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)amino)-2-fluorobenzonitrile

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Technology Process of 5-amino-4-(((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)amino)-2-fluorobenzonitrile

There total 9 articles about 5-amino-4-(((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)amino)-2-fluorobenzonitrile 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: 98.0%

: 1437790-14-1
4-(((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)amino)-2-fluoro-5-nitrobenzonitrile

: 1437790-15-2
5-amino-4-(((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)amino)-2-fluorobenzonitrile

Guidance literature:: With tin(ll) chloride; In ethanol; at 80 ℃; for 3h;
DOI:10.1021/jm4000038

Reference yield:

: 15028-39-4,13226-98-7
L-2-phenylglycine methyl ester hydrochloride

: 1437790-15-2
5-amino-4-(((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)amino)-2-fluorobenzonitrile

Guidance literature:: Multi-step reaction with 6 steps

1.1: 1,2-dichloro-ethane / 0.25 h / 20 °C

1.2: 20 °C

2.1: tetrahydrofuran / 0 - 20 °C / Inert atmosphere

3.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0 - 20 °C

4.1: trifluoroacetic acid / dichloromethane / 3 h / 20 °C

5.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 16 h / 0 - 20 °C / Sealed tube

6.1: tin(ll) chloride / ethanol / 3 h / 80 °C

With N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; tin(ll) chloride; In tetrahydrofuran; ethanol; dichloromethane; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1021/jm4000038

Reference yield:

: 179321-49-4
N-(tert-butoxycarbonyl)-4-aminocyclohexanone

: 1437790-15-2
5-amino-4-(((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)amino)-2-fluorobenzonitrile

Guidance literature:: Multi-step reaction with 6 steps

1.1: 1,2-dichloro-ethane / 0.25 h / 20 °C

1.2: 20 °C

2.1: tetrahydrofuran / 0 - 20 °C / Inert atmosphere

3.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0 - 20 °C

4.1: trifluoroacetic acid / dichloromethane / 3 h / 20 °C

5.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 16 h / 0 - 20 °C / Sealed tube

6.1: tin(ll) chloride / ethanol / 3 h / 80 °C

With N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; tin(ll) chloride; In tetrahydrofuran; ethanol; dichloromethane; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1021/jm4000038