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Indoline → HCID 178418799, 화합물

HRID 7414
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HRID 7414 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.CS[C:12]1[N:17]=[C:16]([OH:18])[C:15]([C:19]([O:21][CH2:22][CH3:23])=[O:20])=[CH:14][N:13]=1>C(O)C>[OH:18][C:16]1[C:15]([C:19]([O:21][CH2:22][CH3:23])=[O:20])=[CH:14][N:13]=[C:12]([N:1]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[CH2:3][CH2:2]2)[N:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10328IndolineHCID 178418871HCID 178418871, 화합물

생성물 1

HCID 178418799HCID 178418799, 화합물수율 77.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of indoline (3.58 g, 30 mmol) in ethanol (50 mL) was added ethyl 2-methylthio-4-hydroxypyrimidine-5-carboxylate (5.35 g, 25 mmol) and the mixture was heated under reflux for 18 h. The reaction mixture was allowed to cool to room temperature and the precipitated crystals were collected by filtration. The crystals were washed several times with cold ethanol and dried to give the title compound (5.5 g, 77%) as crystals.

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temperature
the mixture was heated
  • temperatureunder reflux for 18 h
  • filtrationthe precipitated crystals were collected by filtration
  • washThe crystals were washed several times with cold ethanol
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-b3ebf651e99d40be9d11ee0c8e9016bb
    출처 데이터셋
    uspto-grants-2006_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07087597B1

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