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 | 氯化亚砜 | HCID 24386 | — |
| 反应物 | 2-溴-4-氟苯胺 | HCID 242873 | — |
| 反应物 | 1-Boc-4-哌啶甲酸 | HCID 392871 | — |
| 催化剂 | 4-二甲氨基吡啶(DMAP) | HCID 14284 | — |
| 溶剂 | 吡啶 | HCID 1049 | — |
| 溶剂 | 二氯甲烷 | HCID 6344 | — |
| 产物 | tert-Butyl 4-((2-bromo-4-fluorophenyl)carbamoyl)piperidine-1-carboxylate | HCID 58878481 | — |
反应步骤
Piperidine-1,4-dicarboxylic acid mono-tert-butyl ester (16.5 g, 72.00 mmol) was dissolved in dry methylene chloride (100 mL) and dry pyridine (15 mL). To the reaction mixture was then added thionyl chloride (10.28 g, 86.40 mmol) under nitrogen atmosphere and the reaction mixture was stirred at room temperature for 30 minutes. To the reaction mixture was then added successively, under nitrogen atmosphere, 2-bromo-4-fluoro-phenylamine (15.0 g, 79.00 mmol), dry triethylamine (25.50 g, 252.0 mmol), dry methylene chloride (120 mL), 4-(dimethylamino)pyridine (0.87 g, 7.20 mmol) and the reaction mixture was stirred at room temperature for 24 hours. The reaction mixture was then partitioned with aqueous 2N HCl and tert-butyl methyl ether. The organic layer was washed with aqueous 2N HCl, aqueous NaHCO3, brine, dried with Na2SO4, filtered and the solvent evaporated in vacuo to yield the title compound as a solid.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07655670B2 |
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| 来源数据集 | uspto-grants-2010_02 |
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| ORD ID | ord-8e2005afd5824055b07c184c86d6bd04 |
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| 来源说明 | uspto-grants-2010_02 |
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