1-((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carbonitrile

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Chemical Name:1-((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carbonitrile
CAS No.:1437789-87-1
Molecular Formula:C₂₅H₂₆N₄O₃
Molecular Weight:430.506
Hs Code.:

Synonyms:1-((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carbonitrile

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Chemical Property of 1-((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carbonitrile

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Technology Process of 1-((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carbonitrile

There total 9 articles about 1-((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carbonitrile 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: 12.88%

: 1-((1S,4r)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carbonitrile

: 1437789-87-1
1-((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carbonitrile

: 1-((1S,4r)-4-((R)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carbonitrile

Guidance literature:: With Chiralpak IA; In methanol; diethylamine; Resolution of racemate;

Reference yield:

: 1437790-12-9
3-((4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)amino)-2-nitrobenzonitrile

: 1437789-87-1
1-((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: tin(ll) chloride / ethanol / 2 h / 80 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 20 - 60 °C

With N-ethyl-N,N-diisopropylamine; tin(ll) chloride; In tetrahydrofuran; ethanol;
DOI:10.1021/jm4000038

Reference yield:

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

: 1437789-87-1
1-((1S,4r)-4-((S)-5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)cyclohexyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carbonitrile

Guidance literature:: Multi-step reaction with 7 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 / 80 °C / Sealed tube

6.1: tin(ll) chloride / ethanol / 2 h / 80 °C

7.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 20 - 60 °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