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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1441663생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물2-Bromo-4-fluoroanilineHCID 242873—
반응물1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물tert-Butyl 4-((2-bromo-4-fluorophenyl)carbamoyl)piperidine-1-carboxylateHCID 58878481—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07655670B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-8e2005afd5824055b07c184c86d6bd04
출처 메모uspto-grants-2010_02