(R)-5-chloro-N-(1-(3,5-difluorophenyl)-2-hydroxyethyl)-N-ethylthiophene-2-sulfonamide

Base Information

Chemical Name:(R)-5-chloro-N-(1-(3,5-difluorophenyl)-2-hydroxyethyl)-N-ethylthiophene-2-sulfonamide
CAS No.:1589473-86-8
Molecular Formula:C₁₄H₁₄ClF₂NO₃S₂
Molecular Weight:381.852
Hs Code.:

Synonyms:(R)-5-chloro-N-(1-(3,5-difluorophenyl)-2-hydroxyethyl)-N-ethylthiophene-2-sulfonamide

Suppliers and Price of (R)-5-chloro-N-(1-(3,5-difluorophenyl)-2-hydroxyethyl)-N-ethylthiophene-2-sulfonamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (R)-5-chloro-N-(1-(3,5-difluorophenyl)-2-hydroxyethyl)-N-ethylthiophene-2-sulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-5-chloro-N-(1-(3,5-difluorophenyl)-2-hydroxyethyl)-N-ethylthiophene-2-sulfonamide

There total 6 articles about (R)-5-chloro-N-(1-(3,5-difluorophenyl)-2-hydroxyethyl)-N-ethylthiophene-2-sulfonamide 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: 46.0%

: 1589473-82-4
(R)-5-chloro-N-(1-(3,5-difluorophenyl)-2-hydroxyethyl)thiophene-2-sulfonamide

: 75-03-6
ethyl iodide

: 1589473-86-8
(R)-5-chloro-N-(1-(3,5-difluorophenyl)-2-hydroxyethyl)-N-ethylthiophene-2-sulfonamide

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 12h;
DOI:10.1002/ardp.201300283

Reference yield:

: 1589473-76-6
(R)-4-benzyl-3-(2-(3,5-difluorophenyl)acetyl)oxazolidin-2-one

: 1589473-86-8
(R)-5-chloro-N-(1-(3,5-difluorophenyl)-2-hydroxyethyl)-N-ethylthiophene-2-sulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium hexamethylsilazane / tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

1.2: 0.17 h / -78 °C / Inert atmosphere

2.1: lithium borohydride; water / tetrahydrofuran / 24.5 h / 0 - 20 °C

3.1: palladium 10% on activated carbon; hydrogen / methanol / 4 h / Inert atmosphere

4.1: pyridine / dichloromethane / 0.25 h / 20 °C

4.2: 24 h

5.1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 20 °C

With pyridine; lithium borohydride; palladium 10% on activated carbon; water; hydrogen; potassium hexamethylsilazane; potassium carbonate; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/ardp.201300283

Reference yield:

: 1589473-77-7
(R)-4-benzyl-3-((R)-2-bromo-2-(3,5-difluorophenyl)acetyl)oxazolidin-2-one

: 1589473-86-8
(R)-5-chloro-N-(1-(3,5-difluorophenyl)-2-hydroxyethyl)-N-ethylthiophene-2-sulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium azide / acetonitrile / 7 h / 0 - 20 °C

2.1: lithium borohydride; water / tetrahydrofuran / 24.5 h / 0 - 20 °C

3.1: palladium 10% on activated carbon; hydrogen / methanol / 4 h / Inert atmosphere

4.1: pyridine / dichloromethane / 0.25 h / 20 °C

4.2: 24 h

5.1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 20 °C

With pyridine; lithium borohydride; sodium azide; palladium 10% on activated carbon; water; hydrogen; potassium carbonate; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1002/ardp.201300283