반응 #2275728

반응 방정식

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

용매

DCM

반응 조건

후처리

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

실험 절차

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.

출처