N-(3,4-difluorophenyl)-5-(N-(1-ethylcyclopropyl)sulfamoyl)-2-fluorobenzamide

Base Information

Chemical Name:N-(3,4-difluorophenyl)-5-(N-(1-ethylcyclopropyl)sulfamoyl)-2-fluorobenzamide
CAS No.:1616807-77-2
Molecular Formula:C₁₈H₁₇F₃N₂O₃S
Molecular Weight:398.406
Hs Code.:

Synonyms:N-(3,4-difluorophenyl)-5-(N-(1-ethylcyclopropyl)sulfamoyl)-2-fluorobenzamide

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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 N-(3,4-difluorophenyl)-5-(N-(1-ethylcyclopropyl)sulfamoyl)-2-fluorobenzamide

Chemical Property:

Purity/Quality:

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Technology Process of N-(3,4-difluorophenyl)-5-(N-(1-ethylcyclopropyl)sulfamoyl)-2-fluorobenzamide

There total 3 articles about N-(3,4-difluorophenyl)-5-(N-(1-ethylcyclopropyl)sulfamoyl)-2-fluorobenzamide 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: 45.0%

: 174886-06-7
1-ethylcyclopropylamine hydrochloride

: 1616809-39-2
3-((3,4-difluorophenyl)carbamoyl)-4-fluorobenzene-1-sulfonyl chloride

: 1616807-77-2
N-(3,4-difluorophenyl)-5-(N-(1-ethylcyclopropyl)sulfamoyl)-2-fluorobenzamide

Guidance literature:: With triethylamine; In tetrahydrofuran; at 20 ℃; for 1.5h;

Reference yield:

: 37098-75-2
2-fluoro-5-chlorosulfonylbenzoic acid

: 1616807-77-2
N-(3,4-difluorophenyl)-5-(N-(1-ethylcyclopropyl)sulfamoyl)-2-fluorobenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / 1,2-dichloro-ethane / 1 h / Reflux

2: toluene / 16 h

3: triethylamine / tetrahydrofuran / 1.5 h / 20 °C

With thionyl chloride; triethylamine; In tetrahydrofuran; 1,2-dichloro-ethane; toluene;

Reference yield:

: 949485-81-8
5-(chlorosulfonyl)-2-fluorobenzoyl chloride

: 1616807-77-2
N-(3,4-difluorophenyl)-5-(N-(1-ethylcyclopropyl)sulfamoyl)-2-fluorobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 16 h

2: triethylamine / tetrahydrofuran / 1.5 h / 20 °C

With triethylamine; In tetrahydrofuran; toluene;