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N-methyl-2-pyrrolidone → 7-Methyl-2-oxo-1,2-dihydroquinoline-6-carbonitrile

HRID 1465735
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인쇄 미리보기

반응식

HRID 1465735 반응식
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[CH3:12])[N:8]=[CH:7][CH:6]=[CH:5]2.CN1CCCC1=[O:19].[C:20]([Cu])#[N:21]>O>[CH3:12][C:11]1[CH:10]=[C:9]2[C:4]([CH:5]=[CH:6][C:7](=[O:19])[NH:8]2)=[CH:3][C:2]=1[C:20]#[N:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 13387N-methyl-2-pyrrolidoneHCID 579110186-Bromo-7-methylquinolineHCID 178418546HCID 178418546, 화합물

생성물 1

HCID 916190707-Methyl-2-oxo-1,2-dihydroquinoline-6-carbonitrile

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
20 °C

실험 절차

A mixture of 6-bromo-7-methylquinolin (10 g, 42.0 mmol, prepared following J. Med. Chem. 1988, 31, 2048.), N-methyl-2-pyrrolidinone (32 mL), and CuCN (11 g, 0.13 mol) was stirred at 20° C. overnight and then at reflux temperature (202° C.) for 7 h. The mixture was poured into water (250 mL) and filtered, and the solid was washed twice with water to furnish 7-Methyl-2-oxo-1,2-dihydroquinoline-6-carbonitrile.

후처리

  1. temperatureat reflux temperature (202° C.) for 7 h
  2. filtrationfiltered
  3. washthe solid was washed twice with water

출처 및 근거

ORD 기록
ord-a5f4fe8986354811a32590097edab413
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08999991B2

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