تفاعل #159731

ord-c3d7c6b4b75f47ed8e702c3a4fe3ca59

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىSolvents were evaporated in vacuo
  2. 2
    workup.ADDITIONthe residue was diluted with water (5 ml)
  3. 3
    استخلاصextracted with ethylacetate (3×20 ml)
  4. 4
    أخرىCollected organics, after solvent evaporation
  5. 5
    أخرىafforded a residue that
  6. 6
    غسيلwas washed with methanol
  7. 7
    أخرىdried in vacuo

الإجراء التجريبي

4-(1-(5-chloro-2-(3-(3-fluorobenzoyl)azetidin-1-yl)nicotinamido)cyclopropyl)benzoic acid (E25) (12.6 mg, 0.025 mmol) was dissolved in dry pyridine (1.2 ml) then O-methylhydroxylamine hydrochloride (4.3 mg, 0.051 mmol) was added and the resulting mixture was stirred at room temperature for 60 h. Solvents were evaporated in vacuo, and the residue was diluted with water (5 ml) and extracted with ethylacetate (3×20 ml). Collected organics, after solvent evaporation, afforded a residue that was washed with methanol and dried in vacuo to afford the title compound (E26) (D021/092/2) (3 mg).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08828987B2uspto-grants-2014_09