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2-Chlorophenothiazine → 1-propan-2-yl-10H-phenothiazine

HRID 1626258
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반응식

HRID 1626258 반응식
Cl[C:2]1[CH:15]=[CH:14][C:13]2[S:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[NH:5][C:4]=2[CH:3]=1.[CH2:16]1[CH2:20]OC[CH2:17]1>>[CH:16]([C:3]1[C:4]2[NH:5][C:6]3[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=3)[S:12][C:13]=2[CH:14]=[CH:15][CH:2]=1)([CH3:20])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 70882-ChlorophenothiazineHCID 8028Tetrahydrofuran

생성물 1

HCID 52575471-propan-2-yl-10H-phenothiazine수율 52%

실험 절차

To a solution of 2-chlorophenothiazine (4.67 g, 20 mmol) in anhydrous THF (40 mL) i-propyllithium (0.7 m solution in pentane, 100 mL, 70 mmol) was added at −75° C. (1 h). The reaction mixture had been stirred (2 h), ice-water was added slowly (30 min.) and after that the stirring was continued for 30 min. The organic layer was separated and combined with ether extracts of the aqueous phase. The combined organic phase was washed with water, dried (Na2SO4) and concentrated to give the crude product (52% yield). Compound was purified by flash chromatography (solvent system: hexane-ethyl acetate).

후처리

  1. additionwas added slowly (30 min.)
  2. customThe organic layer was separated
  3. washThe combined organic phase was washed with water
  • dry with materialdried (Na2SO4)
  • concentrationconcentrated
  • 출처 및 근거

    ORD 기록
    ord-2e34f53d44744047aece2e8b185e5292
    출처 데이터셋
    uspto-grants-2014_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08785434B2

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