Reaktion #658268

ord-d00e67e6c0064cadbaed9e1c1d69663e

Reaktionsgleichung

O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCCC(C)C
isohexane
N#N
N2
COc1ccc(I)cc1OC
4-iodo-1,2-dimethoxybenzene
CC(C)(C)c1cc(N)[nH]n1
3-tert-butyl-1H-pyrazol-5-amine
CN[C@@H]1CCCC[C@H]1NC
(1R,2R)—N1,N2-dimethylcyclohexane-1,2-diamine
COc1ccc(-n2nc(C(C)(C)C)cc2N)cc1OC
title compound
COc1ccc(-n2nc(C(C)(C)C)cc2N)cc1OC
3-tert-Butyl-1-(3,4-dimethoxyphenyl)-1H-pyrazol-5-amine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added
  2. 2
    Temperaturthe reaction mixture was heated
  3. 3
    Temperaturat reflux under N2 for 16 hr
  4. 4
    Sonstigewas partitioned between EtOAc (100 mL) and water (150 mL)
  5. 5
    SonstigeThe organic layer was separated
  6. 6
    Waschenwas washed with aq. citric acid solution (10% w/v, 50 mL)
  7. 7
    Sonstigedried
  8. 8
    Sonstigeevaporated in vacuo
  9. 9
    SonstigeThe residue was purified by flash column chromatography (SiO2, 80 g, EtOAc in isohexane, 0-70%, gradient elution)
  10. 10
    SonstigeThe impure product so obtained
  11. 11
    Filtrationthe resulting precipitate was collected by filtration

Vorschrift

To a solution of 4-iodo-1,2-dimethoxybenzene (1.10 g, 4.17 mmol) in anhydrous toluene (5.0 mL) was added 3-tert-butyl-1H-pyrazol-5-amine (638 mg, 4.58 mmol) followed by (1R,2R)—N1,N2-dimethylcyclohexane-1,2-diamine (130 μL, 0.83 mmol) and potassium carbonate (1.15 g, 8.3 mmol). The mixture was purged with N2, copper(I) iodide (40 mg, 0.21 mmol) was added and the reaction mixture was heated at reflux under N2 for 16 hr. The resulting mixture was cooled to RT and was partitioned between EtOAc (100 mL) and water (150 mL). The organic layer was separated and was washed with aq. citric acid solution (10% w/v, 50 mL) followed by brine (50 mL) and then dried and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, 80 g, EtOAc in isohexane, 0-70%, gradient elution). The impure product so obtained was dissolved in ether (1.0 mL), isohexane (10 mL) was added and the resulting precipitate was collected by filtration to afford the title compound, Intermediate A19, as a purple solid (364 mg, 31%); Rt 3.55 min (Method 1); m/z 276 (M+H)+ (ES+).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09024041B2uspto-grants-2015_05