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2-(2-Methoxycarbonyl-phenyl)-6-methyl-4-quinolinecarboxylic acid → HCID 15816898, 화합물

HRID 1956761
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인쇄 미리보기

반응식

HRID 1956761 반응식
[CH3:1][O:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]1[CH:20]=[C:19](C(O)=O)[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([CH3:24])[CH:17]=2)[N:12]=1)=[O:4]>C1(OC2C=CC=CC=2)C=CC=CC=1>[CH3:24][C:16]1[CH:17]=[C:18]2[C:13](=[CH:14][CH:15]=1)[N:12]=[C:11]([C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=1[C:3]([O:2][CH3:1])=[O:4])[CH:20]=[CH:19]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 218016092-(2-Methoxycarbonyl-phenyl)-6-methyl-4-quinolinecarboxylic acid

생성물 1

HCID 15816898HCID 15816898, 화합물수율 66.8%

시약·촉매·용매 1

HCID 7583Diphenyl Ether용매

반응 조건

온도
225 °C

실험 절차

267 mg (0.831 mmol) of 2-(2-methoxycarbonylphenyl)-6-methyl-4-quinolinecarboxylic acid obtained in Example 4 was dissolved in 4.0 ml of diphenyl ether and heated at 225° C. for 10 minutes. After allowing the mixture to cool to room temperature, purification was carried out by flash silica gel chromatography using a mixed solvent of hexane and ethyl acetate (10/1) to obtain 154 mg of methyl 2-(6-methylquinolin-2-yl)benzoate. NMR (270 MHz, CDCl3):

후처리

  1. temperatureto cool to room temperature
  2. custompurification

출처 및 근거

ORD 기록
ord-435a2f6856f04c6baef45afac5c0df84
출처 데이터셋
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05780634

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