Réaction #2275728

Équation de réaction

NaBH(OAc)3

1-(4-oxo-cyclohexyl)-1H-pyridin-2-one

N-(azetidin-3-ylcarbamoylmethyl)-3-trifluoromethyl-benzamide HCl salt

→

N-({1-[4-(2-Oxo-2H-pyridin-1-yl)-cyclohexyl]-azetidin-3-ylcarbamoyl}-methyl)-3-trifluoromethyl-benzamide

Solvants

DCM

Conditions de réaction

Traitement

1. 1
   AutreThe reaction was quenched with saturated sodium bicarbonate
2. 2
   AutreThe organic layer was separated
3. 3
   Extractionthe aqueous layer was extracted 3 times with a chloroform/IPA “cocktail” (˜3:1
4. 4
   SéchageThe combined organic layer was dried over anhydrous Na2SO4
5. 5
   Filtrationfiltered
6. 6
   Concentrationconcentrated
7. 7
   Autreto give the crude product, which
8. 8
   Autrewas then purified by a CombiFlash® system
9. 9
   Autreto afford two title compounds as white solids

Mode opératoire

A solution of 1-(4-oxo-cyclohexyl)-1H-pyridin-2-one (as prepared in the previous step, 150 mg, 0.79 mmol) and N-(azetidin-3-ylcarbamoylmethyl)-3-trifluoromethyl-benzamide HCl salt (as prepared in Example 2 Step C, 400 mg, 1.18 mmol) in DCM (10 mL) was treated with TEA (340 μL, 2.40 mmol) for 10 min followed by NaBH(OAc)3 (Aldrich, 510 mg, 2.40 mmol) for another 4 hours at room temperature. The reaction was quenched with saturated sodium bicarbonate. The organic layer was separated and the aqueous layer was extracted 3 times with a chloroform/IPA “cocktail” (˜3:1, v/v). The combined organic layer was dried over anhydrous Na2SO4, filtered and concentrated to give the crude product, which was then purified by a CombiFlash® system using ethyl acetate and 7N NH3 in MeOH as eluent (from pure ethyl acetate to 5% 7N NH3 in MeOH in ethyl acetate) to afford two title compounds as white solids: a less polar isomer, and a more polar isomer.

Source