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HRID 1441663生成日期:2026年10月24日

三乙胺 → tert-Butyl 4-((2-bromo-4-fluorophenyl)carbamoyl)piperidine-1-carboxylate

https://huagongshe.com/zh-CN/reaction/1441663

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-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
专利号US07655670B2
来源数据集uspto-grants-2010_02
ORD IDord-8e2005afd5824055b07c184c86d6bd04
来源说明uspto-grants-2010_02