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7-Benzyloxy4-(2-methoxyethylsulphanyl)quinazoline → 7-Hydroxy-4-(2-methoxyethylsulphanyl)quinazoline

HRID 1597245
노트
인쇄 미리보기

반응식

HRID 1597245 반응식
C([O:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13]([S:19][CH2:20][CH2:21][O:22][CH3:23])=[N:14][CH:15]=[N:16]2)=[CH:11][CH:10]=1)C1C=CC=CC=1>C(O)(C(F)(F)F)=O>[OH:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13]([S:19][CH2:20][CH2:21][O:22][CH3:23])=[N:14][CH:15]=[N:16]2)=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 216992667-Benzyloxy4-(2-methoxyethylsulphanyl)quinazoline

생성물 1

HCID 1357987517-Hydroxy-4-(2-methoxyethylsulphanyl)quinazoline수율 100.2%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of 7-benzyloxy-4-(2-methoxyethylsulphanyl)quinazoline (8 g, 24.5 mmol) in TFA (80 ml) was refluxed for 5 hours. After cooling and removal of the volatiles by evaporation, the residue was triturated with water, collected by filtration, washed with water and then ethyl acetate. The residue was resuspended in methylene chloride, filtered, washed with petroleum ether and dried under vacuum to give 7-hydroxy-4-(2-methoxyethylsulphanyl)quinazoline (5.8 g, quant.).

후처리

  1. temperature
After cooling
  • customremoval of the volatiles
  • customby evaporation
  • customthe residue was triturated with water
  • filtrationcollected by filtration
  • washwashed with water
  • filtrationfiltered
  • washwashed with petroleum ether
  • customdried under vacuum
  • 출처 및 근거

    ORD 기록
    ord-f15a852f84aa42e3a4e3f8483a3b7d9a
    출처 데이터셋
    uspto-grants-2001_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06294532B1

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