参与物
| 角色 | 名称 | HCID | 投料 |
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| 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)picolinamide | HCID 42645025 | 18% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US08524726B2 |
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| 来源数据集 | uspto-grants-2013_09 |
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| ORD ID | ord-bf9a8f47cc0d45d592b8c2e6d4a9879b |
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| 来源说明 | uspto-grants-2013_09 |
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