Triethylamine → HCID 178441839, Verbindung

HRID 37221

Reaktionsgleichung

Reaktionsgleichung von HRID 37221
[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([CH3:11])=[CH:7][C:3]=1[C:4]([OH:6])=O.C([N:14]([CH2:17][CH3:18])CC)C.[C:19](Cl)(=O)[CH2:20][CH2:21]CC.CCOC(C)=O.CCCCCC>CN(C=O)C.CN(C1C=CN=CC=1)C>[CH2:18]([C:17]1[NH:1][C:2]2[C:3]([C:4](=[O:6])[N:14]=1)=[CH:7][C:8]([CH3:11])=[CH:9][CH:10]=2)[CH2:19][CH2:20][CH3:21]

Komponenten

7

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of 3.0 g (20 mmol) of 2-amino-5-methyl benzoic acid in 20 mL of dry DMF at 0° C. was added 200 mg of DMAP followed by 6.07 g (60 mmol) of triethylamine and 5.02 g (40 mmol) of valeryl chloride. The resulting mixture was stirred at 0° C. for 30 min. The mixture was heated to 110° C. and monitored by TLC for the formation of the intermediate quinoxazolone (Rf =0.8, 40% EtOAc/hexane). Following complete formation of the intermediate 10 g (100 mmol) of (NH4)2CO3 was added cautiously. Heating was continued to ensure consumption of the quinoxazolone and formation of the polar (Rf =0.4, 40% EtOAc/hexane) quinazolin-4(1H)-one. The reaction mixture was concentrated in vacuo and the residue was taken up in 50 mL of ether and 50 mL of water. The mixture was filtered and the filtrate discarded after washing the residue with 20 mL of ether. The residue was recrystalized from MeOH to give 1.07 g (25%) of the title compound as a white crystalline solid.

Aufarbeitung

  1. temperatureThe mixture was heated to 110° C.
  2. additionwas added cautiously
  3. temperatureHeating
  4. customconsumption of the quinoxazolone and formation of the polar (Rf =0.4, 40% EtOAc/hexane) quinazolin-4(1H)-one
  5. concentrationThe reaction mixture was concentrated in vacuo
  6. filtrationThe mixture was filtered
  7. washafter washing the residue with 20 mL of ether
  8. customThe residue was recrystalized from MeOH

Quellen und Nachweise

ORD-Eintrag
ord-e9d62138891645b49a8ad36a194e69d0
Quelldatensatz
uspto-grants-1995_05
Patentnummer
US05420133

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