Benzamidine → HCID 178510335, Verbindung

HRID 33112

Reaktionsgleichung

Reaktionsgleichung von HRID 33112
[C:1]([NH2:9])(=[NH:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([O:12][C:13](=O)[C:14](=[CH:17]OCC)[C:15]#[N:16])C>CN(C=O)C>[OH:12][C:13]1[C:14]([C:15]#[N:16])=[CH:17][N:9]=[C:1]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[N:8]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a stirred solution of benzamidine (1.0 g, 8.32 mmol) in anhydrous DMF (20 mL ) was added Ethyl(ethoxymethylene)cyanoacetate (11) (1.41 g, 8.32 mmol, 1.0 equiv ) under argon at 0° C. The mixture was stirred at 0° C. for 2 h and increase to 105° C. for 60 h. The reaction mixture was then cooled to ambient temperature. The mixture was extracted with ethyl acetate (2×100 mL ). The combined organic extracts were washed with water (1×50 mL) and brine (1×50 mL), dried (Na2SO4), filtered, and evaporated in vacuo. The residue was washed with water (1×60 mL), dichloromethane (1×60 mL) then dried in the vacuum oven to obtain the light yellow solid as product (0.77 g, 47%). 1H-NMR (CD3CN) δ8.25 (s, 1H ), 8.06 (d, 2H ), 7.70 (t, 1H ), 7.61 (t, 2H). MS LC-MS (MH+=198).

Aufarbeitung

  1. temperatureincrease to 105° C. for 60 h
  2. temperatureThe reaction mixture was then cooled to ambient temperature
  3. extractionThe mixture was extracted with ethyl acetate (2×100 mL )
  4. washThe combined organic extracts were washed with water (1×50 mL) and brine (1×50 mL)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. customevaporated in vacuo
  8. washThe residue was washed with water (1×60 mL), dichloromethane (1×60 mL)
  9. customthen dried in the vacuum oven
  10. customto obtain the light yellow solid as product (0.77 g, 47%)

Quellen und Nachweise

ORD-Eintrag
ord-e6425ac839a74fdbb7b9d89eec18c911
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07429584B2

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