Diphenyl Ether → methyl 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylate

HRID 354888

반응식

HRID 354888 반응식
[CH3:1][O:2][C:3](=[O:29])[C:4](=[CH:9][NH:10][C:11]1[C:20]2[C:15](=[CH:16][CH:17]=[C:18]([NH:21][C:22](=[O:28])[CH:23]([CH2:26][CH3:27])[CH2:24][CH3:25])[CH:19]=2)[N:14]=[CH:13][N:12]=1)[C:5](OC)=[O:6].C1(OC2C=CC=CC=2)C=CC=CC=1>CCCCCC>[O:6]=[C:5]1[N:12]2[CH:13]=[N:14][C:15]3[CH:16]=[CH:17][C:18]([NH:21][C:22](=[O:28])[CH:23]([CH2:26][CH3:27])[CH2:24][CH3:25])=[CH:19][C:20]=3[C:11]2=[N:10][CH:9]=[C:4]1[C:3]([O:2][CH3:1])=[O:29]

참가 물질

4

반응 조건

온도
255 °C

실험 절차

A mixture of dimethyl[[6-(2-ethylbutyramido)-4-quinazolinylamino]methylene]propanedioate (5.3 g) and diphenyl ether (32 ml) was heated at 255° C. for 15 minutes and cooled to ambient temperature. Hexane was added to the reaction mixture. The resulting crystals were filtered off, washed with hexane and dried. The crude crystals were dissolved in a mixture of chloroform and methanol (10:1) under heating. Insoluble materials were removed by filtration. The filtrate was concentrated under reduced pressure to give crystals, which were recrystallized from a mixture of chloroform and hexane to give methyl 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylate (3.81 g).

후처리

  1. temperaturecooled to ambient temperature
  2. filtrationThe resulting crystals were filtered off
  3. washwashed with hexane
  4. customdried
  5. dissolutionThe crude crystals were dissolved in a mixture of chloroform and methanol (10:1)
  6. temperatureunder heating
  7. customInsoluble materials were removed by filtration
  8. concentrationThe filtrate was concentrated under reduced pressure
  9. customto give crystals, which
  10. customwere recrystallized from a mixture of chloroform and hexane

출처 및 근거

ORD 기록
ord-c2457fe689d94c68b6796249a04d2da1
출처 데이터셋
uspto-grants-1983_03
특허 번호
US04377580

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