Glycolic Acid → 2-Hydroxymethyl-5-methoxy-3-methylimidazo[5,4-b]pyridine

HRID 1738248Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1738248
[NH2:1][C:2]1[C:3]([NH:10][CH3:11])=[N:4][C:5]([O:8][CH3:9])=[CH:6][CH:7]=1.C(O)(=O)[CH2:13][OH:14].O.[C:18]1(C)C=CC=CC=1>>[OH:14][CH2:13][C:11]1[N:10]([CH3:18])[C:3]2[C:2]([N:1]=1)=[CH:7][CH:6]=[C:5]([O:8][CH3:9])[N:4]=2

Komponenten

5

Edukt 4

HCID 757Glycolic AcidHCID 962WaterHCID 1140TolueneHCID 57437606-methoxy-2-N-methylpyridine-2,3-diamine

Produkt 1

HCID 108216002-Hydroxymethyl-5-methoxy-3-methylimidazo[5,4-b]pyridine

Versuchsvorschrift

A solution of 2.20 g of 3-amino-6-methoxy-2-methylaminopyridine (prepared as described in Preparation 68) and 3.30 g of glycolic acid in 40 ml of toluene was heated under reflux for 4 hours. At the end of this time, the reaction mixture was poured into water, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel, using a 30:1 by volume mixture of ethyl acetate and methanol as the eluent, to give 620 mg of the title compound, melting at 138-140° C.

Aufarbeitung

  1. temperatureunder reflux for 4 hours
  2. extractionafter which it was extracted with ethyl acetate
  3. washThe extract was washed with an aqueous solution of sodium chloride
  4. dry with materialdried over anhydrous sodium sulfate
  5. customafter which the solvent was removed by distillation under reduced pressure
  6. customThe residue was purified by column chromatography through silica gel
  7. additionby volume mixture of ethyl acetate and methanol as the eluent

Quellen und Nachweise

ORD-Eintrag
ord-d540869ba37d4ea3a0611a2d9f4c5963
Quelldatensatz
uspto-grants-1999_10
Patentnummer
US05962470

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