3-chloro-4-fluoro-N-[3-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]propyl]-benzenesulphonamide

Base Information

Chemical Name:3-chloro-4-fluoro-N-[3-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]propyl]-benzenesulphonamide
CAS No.:1365040-89-6
Molecular Formula:C₂₁H₂₂ClF₂N₃O₃S
Molecular Weight:469.94
Hs Code.:

Synonyms:3-chloro-4-fluoro-N-[3-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]propyl]-benzenesulphonamide

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Chemical Property of 3-chloro-4-fluoro-N-[3-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]propyl]-benzenesulphonamide

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Technology Process of 3-chloro-4-fluoro-N-[3-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]propyl]-benzenesulphonamide

There total 4 articles about 3-chloro-4-fluoro-N-[3-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]propyl]-benzenesulphonamide 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: 83.0%

: 131999-32-1
3-[1-(3-aminopropyl)-4-piperidinyl]-6-fluoro-1,2-benzisoxazole

: 91170-93-3
4-fluoro-3-chlorobenzenesulfonyl chloride

: 1365040-89-6
3-chloro-4-fluoro-N-[3-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]propyl]-benzenesulphonamide

Guidance literature:: With triethylamine; In dichloromethane; at 10 - 20 ℃; for 3h;
DOI:10.1021/jm401895u

Reference yield: 83.0%

: 1365040-89-6
3-chloro-4-fluoro-N-[3-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]propyl]-benzenesulphonamide

Guidance literature:

Reference yield:

: 84163-77-9
6-fluoro-3-(4-piperidinyl)benzo[d]isoxazole

: 1365040-89-6
3-chloro-4-fluoro-N-[3-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]propyl]-benzenesulphonamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 48 h / 20 °C

2: methylamine; water / 72 h / 20 °C

3: triethylamine / dichloromethane / 3 h / 10 - 20 °C

With water; potassium carbonate; triethylamine; methylamine; potassium iodide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm401895u