تفاعل #159731
ord-c3d7c6b4b75f47ed8e702c3a4fe3ca59
معادلة التفاعل
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىSolvents were evaporated in vacuo
- 2workup.ADDITIONthe residue was diluted with water (5 ml)
- 3استخلاصextracted with ethylacetate (3×20 ml)
- 4أخرىCollected organics, after solvent evaporation
- 5أخرىafforded a residue that
- 6غسيلwas washed with methanol
- 7أخرىdried 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).