5-chlorothiophene-2-carboxylic acid {(S)-3-[4-(1-methanesulfonyl-4,5-dihydro-1H-imidazole-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}amide

Base Information

Chemical Name:5-chlorothiophene-2-carboxylic acid {(S)-3-[4-(1-methanesulfonyl-4,5-dihydro-1H-imidazole-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}amide
CAS No.:1082936-48-8
Molecular Formula:C₁₉H₁₉ClN₄O₅S₂
Molecular Weight:482.969
Hs Code.:

Synonyms:5-chlorothiophene-2-carboxylic acid {(S)-3-[4-(1-methanesulfonyl-4,5-dihydro-1H-imidazole-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}amide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-chlorothiophene-2-carboxylic acid {(S)-3-[4-(1-methanesulfonyl-4,5-dihydro-1H-imidazole-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}amide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 5-chlorothiophene-2-carboxylic acid {(S)-3-[4-(1-methanesulfonyl-4,5-dihydro-1H-imidazole-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}amide

There total 5 articles about 5-chlorothiophene-2-carboxylic acid {(S)-3-[4-(1-methanesulfonyl-4,5-dihydro-1H-imidazole-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}amide 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: 34.0%

: 1082936-38-6
5-chlorothiophene-2-carboxylic acid {(S)-3-[4-(4,5-dihydro-1H-imidazol-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}amide

: 124-63-0
methanesulfonyl chloride

: 1082936-48-8
5-chlorothiophene-2-carboxylic acid {(S)-3-[4-(1-methanesulfonyl-4,5-dihydro-1H-imidazole-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}amide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 6h;

Reference yield:

: 1082937-32-3
[(S)-3-(4-cyanophenyl)-2-oxo-oxazolidin-5-ylmethyl]-carbamic acid tert-butyl ester

: 1082936-48-8
5-chlorothiophene-2-carboxylic acid {(S)-3-[4-(1-methanesulfonyl-4,5-dihydro-1H-imidazole-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / 1,4-dioxane; ethyl acetate / 1 h / 20 °C

2.1: benzotriazol-1-ol; triethylamine; diisopropyl-carbodiimide / N,N-dimethyl-formamide / 12 h / 20 °C

3.1: hydrogenchloride / methanol / 2.5 h / 0 - 20 °C

3.2: 12 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 6 h / 20 °C

With hydrogenchloride; benzotriazol-1-ol; triethylamine; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide; In 1,4-dioxane; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 1027385-05-2
(S)-5-chloro-N-((3-(4-cyanophenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide

: 1082936-48-8
5-chlorothiophene-2-carboxylic acid {(S)-3-[4-(1-methanesulfonyl-4,5-dihydro-1H-imidazole-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}amide

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogenchloride / methanol / 2.5 h / 0 - 20 °C

1.2: 12 h / 20 °C

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 6 h / 20 °C

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;