Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydroxyamine hydrochloride → 2-Oxo-1,2-dihydroquinoline-3-carbonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 반응물 | Sodium Formate | HCID 2723810 | — |
| 반응물 | 3-Chloroquinoline-2-carbaldehyde | HCID 18467053 | — |
| 용매 | Formic Acid | HCID 284 | — |
| 생성물 | 2-Oxo-1,2-dihydroquinoline-3-carbonitrile | HCID 2764577 | — |
반응 단계
Where the starting material above is a 2-chloro-3-cyanoquinoline, this can be prepared by starting from an appropriate substituted acetanilide. This is heated with phosphoryl chloride and dimethylformamide to give the corresponding 2-chloro-3-quinolinecarboxaldehyde. The process involved is discussed in detail by meth-Cohn et al., J. Chem. Soc., Perkin Trans. 1, 1981, 1520. The chloroquinolinecarboxaldehyde is then reacted with hydroxylamine hydrochloride, formic acid and sodium formate with heating to give the corresponding 3-cyano-2(1H)-quinolinone. This is then heated with an excess of phosphoryl chloride to give the desired 2-chloro-3-cyanoquinoline.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04496569 |
| 출처 데이터셋 | uspto-grants-1985_01 |
| ORD ID | ord-f3baa133583e4eefada2d25af48ae68d |
| 출처 메모 | uspto-grants-1985_01 |