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HRID 38249生成日期:2026年10月23日

三乙胺 → N-(3-chloro-4-(4-isobutyrylpiperazin-1-yl)phenyl)picolinamide

https://huagongshe.com/zh-CN/reaction/38249

反应方程式

参与物

角色名称HCID投料
反应物三乙胺HCID 8471—
反应物吡啶-2-甲酰氯盐酸盐HCID 135033—
反应物1-[4-(4-氨基-2-氯-苯基)-哌嗪-1-基]-2-甲基-丙-1-酮HCID 936926—
溶剂二氯甲烷HCID 6344—
产物N-(3-chloro-4-(4-isobutyrylpiperazin-1-yl)phenyl)picolinamideHCID 4264502518%

反应步骤

According to Scheme 4 Step 3: Picolinoyl chloride hydrochloride (0.93 mmol, 178 mg) and Et3N (1.86 mmol, 0.26 mL) were added to a solution of 1-(4-(4-amino-2-chlorophenyl)piperazin-1-yl)-2-methylpropan-1-one (0.62 mmol, 175 mg) in DCM (3 mL) at 0° C. The reaction mixture was stirred at room temperature for 2 hours. The organic phase was washed with a saturated solution of NaHCO3. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over Na2SO4, was filtered and was concentrated under reduced pressure. The crude product was purified by flash chromatography over C18 column using water/ACN (60:40) as eluent to afford N-(3-chloro-4-(4-isobutyrylpiperazin-1-yl)phenyl)picolinamide (0.11 mmol, 42 mg, 18%) as a white solid.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08524726B2
来源数据集uspto-grants-2013_09
ORD IDord-bf9a8f47cc0d45d592b8c2e6d4a9879b
来源说明uspto-grants-2013_09