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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 888008생성일: 2026년 10월 26일

Hydrochloric Acid → N-(2-Aminophenyl)-4-piperidin-4-ylbenzamide

https://huagongshe.com/reaction/888008

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물N-(2-t-butoxycarbonylaminophenyl)-4-(1-t-butoxycarbonylpiperidin-4-yl)benzamideHCID 68407604—
용매1,4-DioxaneHCID 31275—
생성물N-(2-Aminophenyl)-4-piperidin-4-ylbenzamideHCID 1622558482%

반응 단계

A 4M solution of hydrogen chloride in dioxane (5 ml, 20 mmol) was added to a stirred solution of N-(2-t-butoxycarbonylaminophenyl)-4-(1-t-butoxycarbonylpiperidin-4-yl)benzamide (Method 15, 693 mg, 1.40 mmol) in 1,4-dioxane (5 ml) and the mixture stirred at ambient temperature for 18 hours. The resultant precipitate was filtered and washed with diethyl ether. The resultant solid was dissolved in water and basified to pH 12 with 2M solution of aqueous sodium hydroxide. The resultant precipitate was filtered, washed with water and dried in vacuo to give the title compound (338 mg, 82%); NMR Spectrum: (DMSO-d6) 1.52 (m, 2H), 1.69 (m, 2H), 2.60 (m, 3H), 3.02 (m, 2H), 4.84 (br, 2H), 6.58 (m, 1H), 6.76 (d, 1H), 6.95 (m, 1H), 7.16 (d, 1H), 7.34 (d, 2H), 7.89 (d, 2H), 9.53 (br, 1H); Mass Spectrum: M+H+ 296.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08247562B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-cdb7e8ef782046b68c8b4e2280a0456b
출처 메모uspto-grants-2012_08