benzyl 6-chloro-2-fluoro-3-(N-(propylsulfonyl)propylsulfonamido)benzoate

Base Information

Chemical Name:benzyl 6-chloro-2-fluoro-3-(N-(propylsulfonyl)propylsulfonamido)benzoate
CAS No.:1186194-02-4
Molecular Formula:C₂₀H₂₃ClFNO₆S₂
Molecular Weight:491.989
Hs Code.:

Synonyms:benzyl 6-chloro-2-fluoro-3-(N-(propylsulfonyl)propylsulfonamido)benzoate

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Chemical Property of benzyl 6-chloro-2-fluoro-3-(N-(propylsulfonyl)propylsulfonamido)benzoate

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Technology Process of benzyl 6-chloro-2-fluoro-3-(N-(propylsulfonyl)propylsulfonamido)benzoate

There total 4 articles about benzyl 6-chloro-2-fluoro-3-(N-(propylsulfonyl)propylsulfonamido)benzoate 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: 72.0%

: 918523-46-3
benzyl 2-fluoro-3-amino-6-chlorobenzoate

: 10147-36-1
n-propanesulfonyl chloride

: 1186194-02-4
benzyl 6-chloro-2-fluoro-3-(N-(propylsulfonyl)propylsulfonamido)benzoate

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃;

Reference yield:

: 57946-56-2
2-fluoro-4-chloroaniline

: 501-53-1,94274-21-2
benzyl chloroformate

: 1186194-02-4
benzyl 6-chloro-2-fluoro-3-(N-(propylsulfonyl)propylsulfonamido)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran; hexanes / 0.58 h / -78 °C

1.2: 3.42 h / -78 - 20 °C

1.3: 1 h / -78 °C

2.1: triethylamine / dichloromethane / 0 °C

With n-butyllithium; triethylamine; In tetrahydrofuran; hexanes; dichloromethane;

Reference yield:

: 57946-56-2
2-fluoro-4-chloroaniline

: 1186194-02-4
benzyl 6-chloro-2-fluoro-3-(N-(propylsulfonyl)propylsulfonamido)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran; hexanes / 0.58 h / -78 °C

1.2: 3.42 h / -78 - 20 °C

1.3: 1 h / -78 °C

2.1: triethylamine / dichloromethane / 0 - 20 °C

With n-butyllithium; triethylamine; In tetrahydrofuran; hexanes; dichloromethane;