Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-(Piperidine-1-carbonyl)aniline → 1-[2-(2-Methyl-4-pyridinylamino)benzoyl]piperidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-(Piperidine-1-carbonyl)aniline | HCID 558730 | — |
| 반응물 | 4-Chloro-2-methylpyridine | HCID 581392 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 1-[2-(2-Methyl-4-pyridinylamino)benzoyl]piperidine | HCID 20235851 | 9.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04610991 |
| 출처 데이터셋 | uspto-grants-1986_09 |
| ORD ID | ord-3a247d4932c8499db59017a7574b9655 |
| 출처 메모 | uspto-grants-1986_09 |