Reaktion #4371

Reaktionsgleichung

methyl trans-2-[3-(3,4-dihydro-4-oxobenzofuro[3,2-d]pyrimidin-3-yl)-2-oxopropyl]-3-methoxy-1-piperidinecarboxylate

hydrobromic acid

→

title compound

trans-3-[3-(3-Hydroxy-2-piperidyl)-2-oxopropyl]benzofuro[3,2-d]pyrimidin-4(3H)-one Dihydrobromide

Lösungsmittel

ethanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigepreheated to 150° C.
2. 2
   Sonstigethe solution was evaporated under reduced pressure
3. 3
   Sonstigeto afford a residue
4. 4
   Temperaturto cool
5. 5
   Sonstigethe ethanol removed by pipette

Vorschrift

A solution of 0.600 g (0.00145 mole) of methyl trans-2-[3-(3,4-dihydro-4-oxobenzofuro[3,2-d]pyrimidin-3-yl)-2-oxopropyl]-3-methoxy-1-piperidinecarboxylate and 30 ml of 48% hydrobromic acid in a 100 ml round bottom flask was immersed in a bath preheated to 150° C. and held there for 12 minutes. Upon cooling to room temperature, the solution was evaporated under reduced pressure to afford a residue. The residue was heated with ethanol briefly; the mixture was allowed to cool, and the ethanol removed by pipette to furnish the title compound: m.p. 257°-258° C.; yield 0.28 g (41%); 1H-nmr (DMSO-d6) delta 1.4-2.0 ppm (multiplet, 4H, CH3OCHCH2CH2CH2N), 2.8-3.0 (multiplet, 2H, NCH2), 3.1-3.5 (multiplet, includes H2O, CHOH, COCH2CH, and CH2CHNCO), 5.2 (singlet, 2H, NCH2CO), 7.5 (triplet, 1H, aromatic H), 7.7 (triplet, 1H, aromatic H), 7.9 (doublet, 1H, aromatic H), 8.1 (doublet, 1H, aromatic H), 8.4 (singlet, 1H, N=CH--N), 8.7 (broad singlet, 1H, OH).

Quelle