Chloroacetaldehyde → 6-Iodoimidazo(1,2-a)pyridine

HRID 1372471Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1372471
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([I:8])=[CH:4][N:3]=1.Cl[CH2:10][CH:11]=O>C(O)C>[I:8][C:5]1[CH:6]=[CH:7][C:2]2[N:3]([CH:10]=[CH:11][N:1]=2)[CH:4]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
85 °C

Versuchsvorschrift

To a solution of the product (480 mg, 2.18 mmol) from Step A in ethanol (12 mL) was added chloroacetaldehyde (50 wt. % in water, 0.336 mL) and the mixture was heated at 85° C. for 3 h. After cooling to room temperature, the solution was concentrated under reduced pressure. The residue was partitioned between saturated aqueous sodium bicarbonate solution and dichloromethane. The organic phase was separated, dried (magnesium sulfate) and concentrated in vacuo to yield the product as light-brown solid which was used without further purification. LC/MS 244.8 (M+1).

Aufarbeitung

  1. temperatureAfter cooling to room temperature
  2. concentrationthe solution was concentrated under reduced pressure
  3. customThe residue was partitioned between saturated aqueous sodium bicarbonate solution and dichloromethane
  4. customThe organic phase was separated
  5. dry with materialdried (magnesium sulfate)
  6. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-f62ae5d5d6eb44ff81bb1d6abc7e2e5f
Quelldatensatz
uspto-grants-2007_01
Patentnummer
US07157490B2

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