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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64890생성일: 2026년 10월 24일

2-(Piperidine-1-carbonyl)aniline → 1-[2-(2-Methyl-4-pyridinylamino)benzoyl]piperidine

https://huagongshe.com/ko/reaction/64890

반응식

참여 물질

역할이름HCID투입량
반응물2-(Piperidine-1-carbonyl)anilineHCID 558730—
반응물4-Chloro-2-methylpyridineHCID 581392—
용매Acetic AcidHCID 176—
생성물1-[2-(2-Methyl-4-pyridinylamino)benzoyl]piperidineHCID 202358519.8%

반응 단계

A mixture of 18.2 g of 1-(2-aminobenzoyl)piperidine and 12.2 g of 2-methyl-4-chloropyridine in 5.0 ml of acetic acid was heated at reflux for six hours and then kept at room temperature overnight. The reaction mixture was concentrated in vacuo, and the residue treated with dilute acid to pH 2 and extracted with methylene dichloride. The aqueous layer was made basic with potassium carbonate and extracted with chloroform. Further work-up of this solution afforded 2.58 g of 1-[2-(2-methyl-4-pyridinylamino)benzoyl]piperidine, m.p. 93°-95° C. when recrystallized from ethyl acetate--ether--hexane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04610991
출처 데이터셋uspto-grants-1986_09
ORD IDord-3a247d4932c8499db59017a7574b9655
출처 메모uspto-grants-1986_09