Ethyl 2-chloroacetoacetate → Ethyl 7-methoxy-2-methylimidazo[1,2-a]pyridine-3-carboxylate

HRID 2076240Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2076240
OC1C=CN2C(C(NC)=O)=C(C)N=C2C=1.[CH3:16][O:17][C:18]1[CH:23]=[CH:22][N:21]=[C:20]([NH2:24])[CH:19]=1.Cl[CH:26]([C:32](=O)[CH3:33])[C:27]([O:29][CH2:30][CH3:31])=[O:28]>C(O)C>[CH3:16][O:17][C:18]1[CH:23]=[CH:22][N:21]2[C:26]([C:27]([O:29][CH2:30][CH3:31])=[O:28])=[C:32]([CH3:33])[N:24]=[C:20]2[CH:19]=1

Komponenten

5

Versuchsvorschrift

Note that 7-hydroxy-N,2-dimethylimidazo[1,2-α]pyridine-3-carboxamide 111-B was obtained by the following procedure. To a solution of 4-methoxypyridin-2-amine (prepared as in Org. Prep. & Proc. Int., 29, 1, 117-122, 1997) 2.8 g, 22.6 mmol in ethanol (100 ml) was added ethyl 2-chloro-3-oxobutanoate (6.2 ml, 45.2 mmol) and the resulting solution heated to reflux for 16 hours under a nitrogen atmosphere. The solvents were removed in-vacuo and the yellow solid was titrated with dichloromethane to extract the crude product. The dichloromethane extracts were concentrated and purified by flash chromatography (eluting with ethyl acetate) to yield ethyl 7-methoxy-2-methylimidazo[1,2-α]pyridine-3-carboxylate, 2 g, 38%, as a yellow solid.

Aufarbeitung

  1. customwas obtained by the following procedure
  2. temperaturethe resulting solution heated
  3. temperatureto reflux for 16 hours under a nitrogen atmosphere
  4. customThe solvents were removed in-vacuo
  5. extractionto extract the crude product
  6. concentrationThe dichloromethane extracts were concentrated
  7. custompurified by flash chromatography (eluting with ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-c3ef833701c440b381ea38408143b629
Quelldatensatz
uspto-grants-2011_04
Patentnummer
US07923457B2

Notizen zur Reaktion

Wird geladen…