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Chloroacetaldehyde → 4-(2-{5-[3-(3-Fluoro-phenyl)-2-oxo-imidazolidin-1-yl]-2-methyl-phenylamino}-oxazol-5-yl)-benzonitrile

HRID 244592
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HRID 244592 반응식
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:22])=[C:6]([NH:8][C:9]2[O:10][C:11]([C:14]3[CH:21]=[CH:20][C:17]([C:18]#[N:19])=[CH:16][CH:15]=3)=[CH:12][N:13]=2)[CH:7]=1.Cl[CH2:24][CH:25]=O.[BH3-]C#N.[Na+].C([O-])(O)=O.[Na+].[F:36][C:37]1[CH:42]=[CH:41][CH:40]=[C:39]([N:43]=[C:44]=[O:45])[CH:38]=1.CC(C)([O-])C.[K+]>C(#N)C.C1(C)C=CC=CC=1.O.C(OCC)(=O)C.C(O)(=O)C>[F:36][C:37]1[CH:38]=[C:39]([N:43]2[CH2:25][CH2:24][N:1]([C:2]3[CH:3]=[CH:4][C:5]([CH3:22])=[C:6]([NH:8][C:9]4[O:10][C:11]([C:14]5[CH:21]=[CH:20][C:17]([C:18]#[N:19])=[CH:16][CH:15]=5)=[CH:12][N:13]=4)[CH:7]=3)[C:44]2=[O:45])[CH:40]=[CH:41][CH:42]=1
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참가 물질

12

반응물 6

HCID 33ChloroacetaldehydeHCID 1230643-Fluorophenyl isocyanateHCID 516892Sodium BicarbonateHCID 5003444Sodium cyanoborohydrideHCID 177573464-[2-(5-Amino-2-methyl-phenylamino)-oxazol-5-yl]-benzonitrileHCID 23665647Potassium tert-butoxide

생성물 1

HCID 11965364
4-(2-{5-[3-(3-Fluoro-phenyl)-2-oxo-imidazolidin-1-yl]-2-methyl-phenylamino}-oxazol-5-yl)-benzonitrile
수율 45%

시약·촉매·용매 5

HCID 176Acetic Acid용매HCID 962Water용매HCID 1140Toluene용매HCID 6342Acetonitrile용매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 4-[2-(5-Amino-2-methyl-phenylamino)-oxazol-5-yl]-benzonitrile (558 mg, 2 mmol) and chloroacetaldehyde (50 wt. % in water, 628 mg, 4 mmol) in acetonitril (60 mL), was added at RT NaBH3CN (253 mg, 4 mmol) and dropwise acetic acid (0.4 mL). The mixture was stirred at room temperature 1 h. Ethyl acetate (50 mL) and saturated aqueous NaHCO3 (50 mL) were added. The organic layer was washed with brine (20 mL), dried over MgSO4 and concentrated to give a yellow solid. This was dissolved in toluene (40 mL) and treated with 1-Fluoro-3-isocyanato-benzene (274 mg, 2 mmol) at reflux for 2 h. After evaporation of solvent under reduced vacuum, the crude product was dissolved in isopropanol (60 mL) and treated with potassium tert-butoxide (1.8 g, 16 mmol) at RT for 5 h. Water (20 mL) was added, the organic layer was separated dried over MgSO4 and concentrated. The crude product was silica gel column chromatographed (dichloromethane/ethanol: 95/5) to give 408 mg (45%) of the title compound as a beige solid.

후처리

  1. washThe organic layer was washed with brine (20 mL)
  2. dry with materialdried over MgSO4
  3. concentrationconcentrated
  4. customto give a yellow solid
  5. temperatureat reflux for 2 h
  6. customAfter evaporation of solvent under reduced vacuum
  7. dissolutionthe crude product was dissolved in isopropanol (60 mL)
  8. customthe organic layer was separated
  9. dry with materialdried over MgSO4
  10. concentrationconcentrated
  11. customchromatographed (dichloromethane/ethanol: 95/5)

출처 및 근거

ORD 기록
ord-edc51a882ed8418e8057a0815757bbe6
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658659B2

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