Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyridine → N-[[[1-(6-Fluoro-2-naphthalenylmethyl)-4-piperidinyl]amino]carbonyl]-6-quinoline carboxamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Quinoline-6-carbonyl chloride | HCID 12391963 | — |
| 반응물 | N-[[(6-fluoro-2-naphthalenyl)methyl]-4-piperidinyl]urea | HCID 21288076 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | N-[[[1-(6-Fluoro-2-naphthalenylmethyl)-4-piperidinyl]amino]carbonyl]-6-quinoline carboxamide | HCID 13853618 | — |
반응 단계
A mixture of 6-quinolinoyl chloride (4.77 g, 22 mmol), N-[[(6-fluoro-2-naphthalenyl)methyl]-4-piperidinyl]urea (6.02 g, 20 mmol), dry pyridine (2.5 ml) and 1,2-dichloroethane (30 ml) is stirred at reflux for 18 hours. The solution is then cooled, washed with aqueous sodium carbonate solution, dried and evaporated. The residue is crystallised from ethanol to give the title compound, mp 200°-201° C. (softens, maleate salt).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04778802 |
| 출처 데이터셋 | uspto-grants-1988_10 |
| ORD ID | ord-fe4ffe43b4e3413780803c628c8a457f |
| 출처 메모 | uspto-grants-1988_10 |