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HCID 178506251, 화합물 → HCID 178457431, 화합물

HRID 1285564
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HRID 1285564 반응식
[O:1]1[CH2:20][CH:2]1[CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[NH:12][CH:13]=[C:14]([C:16]([F:19])([F:18])[F:17])[N:15]=2)=[CH:7][CH:6]=1>C(N)(C)C>[CH:14]([NH:15][CH2:20][CH:2]([OH:1])[CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[NH:12][CH:13]=[C:14]([C:16]([F:19])([F:18])[F:17])[N:15]=2)=[CH:7][CH:6]=1)([CH3:16])[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178506251HCID 178506251, 화합물

생성물 1

HCID 178457431HCID 178457431, 화합물

시약·촉매·용매 1

HCID 6363Isopropylamine용매

실험 절차

A solution of 2-[4-(2.3-epoxypropoxy)phenyl]-4-trifluoromethylimidazole (1 g) in isopropylamine (10 ml.) is heated 7 hours at reflux and then allowed to stand 16 hours at room temperature. The excess isopropylamine is removed by distillation at atmospheric pressure and the residue is triturated with nitromethane to yield a solid. After filtration and recrystallization from acetonitrile, 0.6 g. of 2-[4-(3-isopropylamino-2-hydroxypropoxy)phenyl]-4-trifluoromethylimidazole is obtained, m.p. 173°-173.5° C.

후처리

  1. temperatureat reflux
  2. customThe excess isopropylamine is removed by distillation at atmospheric pressure
  3. customthe residue is triturated with nitromethane
  • customto yield a solid
  • filtrationAfter filtration and recrystallization from acetonitrile, 0.6 g
  • 출처 및 근거

    ORD 기록
    ord-587f49d67733431d932887c1cb00624e
    출처 데이터셋
    uspto-grants-1986_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04567276

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