Reaktion #682598

Reaktionsgleichung

2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carboxylic acid

thionyl chloride

Sodium azide

→

2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carbonyl azide

Lösungsmittel

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThionyl chloride was removed under reduced pressure
2. 2
   workup.DISSOLUTIONThe resulting solid acid chloride was dissolved in acetone (15 mL)
3. 3
   workup.ADDITIONwas added to the reaction mixture at 0° C.
4. 4
   TemperaturThe reaction temperature was raised to room temperature
5. 5
   workup.STIRRINGstirred for 5 h
6. 6
   EinengenThe reaction mixture was concentrated
7. 7
   Sonstigeto remove the solvent
8. 8
   SonstigeThe compound precipitated in the aqueous layer
9. 9
   Filtrationwas filtered
10. 10
    Sonstigedried under vacuum

Vorschrift

2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carboxylic acid (30a) (750 mg, 2.54 mmol) and thionyl chloride (12.68 mmol) were refluxed at 100° C. for 20 h. Thionyl chloride was removed under reduced pressure. The resulting solid acid chloride was dissolved in acetone (15 mL) and cooled to 0° C. Sodium azide (7.61 mmol) dissolved in water (3 mL) was added to the reaction mixture at 0° C. and stirred for 30 min. The reaction temperature was raised to room temperature and stirred for 5 h. The reaction mixture was concentrated to remove the solvent. The compound precipitated in the aqueous layer was filtered and dried under vacuum to obtain the desired compound 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carbonyl azide. LC/MS: ZORBAX SB C18, 4.6×50 mm, 5 μm; Solvent A=10% MeOH: 90% H2O: 0.1% TFA; Solvent B=90% MeOH: 10% H2O: 0.1% TFA; gradient 0-100% B over 2 min (3 min run time); retention time: 2.363 min.

Quelle