Water → HCID 44252387, Verbindung

HRID 1477184Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1477184
[CH2:1]([C:8]1([CH2:19][N:20]([CH3:22])[CH3:21])[CH2:13][CH2:12][C:11]([N:16]([CH3:18])[CH3:17])([C:14]#N)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:23]1([Mg]Cl)[CH:28]=[CH:27]C=[CH:25][CH:24]=1.[NH4+].[Cl-].O>C1COCC1>[CH2:1]([C:8]1([CH2:19][N:20]([CH3:21])[CH3:22])[CH2:13][CH2:12][C:11]([N:16]([CH3:17])[CH3:18])([C:14]2[CH:27]=[CH:28][CH:23]=[CH:24][CH:25]=2)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

6

Versuchsvorschrift

The title compound of step 1 (0.88 g, 2.94 mmol) was dissolved in THF (35 mL) and mixed in drops with 2M phenylmagnesium chloride solution (5.1 mL, 10.2 mmol) with ice cooling. The reaction solution was heated to boiling for 8 h. For work up the solution was mixed with 20% NH4Cl solution (0.6 mL) and water (0.4 mL) with ice cooling, extracted with ether (3×25 mL), the ether solution was washed with water, dried (Na2SO4) and concentrated to low volume in a vacuum. The residue was purified by column chromatography with EtOH/EE (1:20). 2 fractions were obtained, wherein according to LCMS, inter alia, the more polar fraction (300 mg) contained the desired substance.

Aufarbeitung

  1. temperatureThe reaction solution was heated
  2. extractionextracted with ether (3×25 mL)
  3. washthe ether solution was washed with water
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated to low volume in a vacuum
  6. customThe residue was purified by column chromatography with EtOH/EE (1:20)
  7. custom2 fractions were obtained

Quellen und Nachweise

ORD-Eintrag
ord-cd4c1ad24bee4d3e80470eaff39787ce
Quelldatensatz
uspto-grants-2016_08
Patentnummer
US09403767B2

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