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HRID 1441663作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/1441663

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Thionyl ChlorideHCID 24386—
反応物2-Bromo-4-fluoroanilineHCID 242873—
反応物1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物tert-Butyl 4-((2-bromo-4-fluorophenyl)carbamoyl)piperidine-1-carboxylateHCID 58878481—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07655670B2
出典データセットuspto-grants-2010_02
ORD IDord-8e2005afd5824055b07c184c86d6bd04
出典メモuspto-grants-2010_02