Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List Sarolaner

Sarolaner synthesis

4synthesis methods
-

Yield:-

Reaction Conditions:

Stage #1:2-(methylsulfonyl)acetic acid;5'-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-3'H-spiro[azetidine-3,1'-isobenzofuran] besylate with triethylamine in ethyl acetate at 18 - 22; for 0.5 h;
Stage #2: with 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide in ethyl acetate at 10 - 35;

Steps:

1 Example 1 : 1 -(5'-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5- dihydroisoxazol-3-yl)-3'H-spiro[azetidine-3,1 '-isobenzofuran]-1 -yl)-2- (methylsulfonyl)ethanone.
Alternatively, the racemate of the besylate salt of the sulfonamide can be removed by mixing methanesulfonylacetic acid (0.615g, 1 .3eq) with the sulfonamide (2.1 g) in 9.3 mL ethyl acetate (EtOAc). Triethylamine is added dropwise over 1 minute (0.825g, 2.4eq) at about 18-22°C. The addition funnel is rinsed with 0.5 mL EtOAc and the resulting mixture is stirred for 30 minutes and cooled to <10°C. To this mixture, 4.313g n-propylphosphonic anhydride (50 weight% in EtOAc), 2.0eq) is added dropwise over 15 minutes at <10°C. The addition funnel is rinsed again with 1 .5 mL EtOAc. The reaction mixture is warmed to 35°C and stirred overnight. (UPLC >97% with <1 % starting material). To the reaction was added 1 .0g Celite filter aid (50% loading) and filtered through a 1 g celite plug in a 15 mL coarse frit glass funnel (1 .75 minute filtration) and rinsed with 4 mL EtOAc (2x). Chiral HPLC 98.8% S enantiomer, 1 .2% R; UPLC >97%, filtrate volume = 18 mL).

References:

ZOETIS LLC;WENDT, John, Adam;ASPER, David, Jose WO2014/39422, 2014, A1 Location in patent:Page/Page column 35