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HRID 856073생성일: 2026년 10월 26일

Tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate → N-(4-chlorophenyl)piperidin-4-amine

https://huagongshe.com/reaction/856073

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylateHCID 1491503—
용매DichloromethaneHCID 6344—
용매Trifluoroacetic acidHCID 6422—
생성물N-(4-chlorophenyl)piperidin-4-amineHCID 7183033—

반응 단계

Tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate (2.67 g, 8.59 mmol) prepared in Reference Example 131 was dissolved in methylene chloride (20 ml), to which trifluoroacetic acid (15 ml) was added dropwise, and the mixture was stirred at room temperature for 5 hours. The reaction mixture was concentrated under reduced pressure, and the residue was then dissolved in methylene chloride. This solution was neutralized with sodium hydroxide aqueous solution, and the mixture was extracted with methylene chloride. The extract was washed with brine, dried over magnesium sulfate, and then filtered. The filtrate was concentrated under reduced pressure to afford 4-(4-chlorophenylamino)piperidine as a pale yellow powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07262212B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-b7e0b26ef41843808d9e512db4e5bd34
출처 메모uspto-grants-2007_08