Hydrochloric Acid → (+)-2-(4-(1-Propanoyloxyethyl)phenyl}-5-decyloxypyrimidine

HRID 1938110

Reaktionsgleichung

Reaktionsgleichung von HRID 1938110
N1C=CC=CC=1.[OH:7][CH:8]([C:10]1[CH:15]=[CH:14][C:13]([C:16]2[N:21]=[CH:20][C:19]([O:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[CH:18][N:17]=2)=[CH:12][CH:11]=1)[CH3:9].[C:33](Cl)(=[O:36])[CH2:34][CH3:35].Cl>O>[C:33]([O:7][CH:8]([C:10]1[CH:11]=[CH:12][C:13]([C:16]2[N:21]=[CH:20][C:19]([O:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[CH:18][N:17]=2)=[CH:14][CH:15]=1)[CH3:9])(=[O:36])[CH2:34][CH3:35]

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 1049PyridineHCID 62324Propionyl chlorideHCID 214682802-(4-(1-Hydroxyethyl)phenyl)-5-decyloxypyrimidine

Produkt 1

HCID 21468270(+)-2-(4-(1-Propanoyloxyethyl)phenyl}-5-decyloxypyrimidineAusbeute 97 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Into 20 ml of pyridine were dissolved 1.78 g (5 millimole) of the (+)-2-{4-(1-hydroxyethyl)phenyl}-5-decyloxypyrimidine obtained in the Preparation Example [starting material compound (VI)] 70, and then 0.56 g (6 millimole) of propionic chloride was added thereto, to subject to reaction at 30° to 40° C. for 2 hours. After completion of the reaction, the reaction mixture was poured into 200 ml of water, adjusted to pH 1 to 2 with 4N hydrochloric acid, and then extracted with 200 ml of toluene, followed by separation thereof. The organic phase was washed with water, 5% aqueous sodium hydrogen carbonate solution and water in this order. After drying over anhydrous magnesium sulfate, the residue obtained by distilling the organic solvent off under reduced pressure was purified by silica gel column chromatography (eluent; toluene:ethyl acetate) to obtain 2.00 g (yield: 97%) of (+)-2-{4-(1-Propanoyloxyethyl)phenyl}-5-decyloxypyrimidine.

Aufarbeitung

  1. customto subject to reaction at 30° to 40° C. for 2 hours
  2. customAfter completion of the reaction
  3. extractionextracted with 200 ml of toluene
  4. customfollowed by separation
  5. washThe organic phase was washed with water, 5% aqueous sodium hydrogen carbonate solution and water in this order
  6. dry with materialAfter drying over anhydrous magnesium sulfate
  7. customthe residue obtained
  8. distillationby distilling the organic solvent off under reduced pressure
  9. customwas purified by silica gel column chromatography (eluent; toluene:ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-32fce9d0742b45b0a168a623e8ef4054
Quelldatensatz
uspto-grants-1997_12
Patentnummer
US05693251

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