Methanol → 4-Chloro-N-methylpicolinamide

HRID 387425

Reaktionsgleichung

Reaktionsgleichung von HRID 387425
Cl.C[O:3][C:4]([C:6]1[CH:11]=[C:10]([Cl:12])[CH:9]=[CH:8][N:7]=1)=O.CO.[CH3:15][NH2:16]>O1CCCC1>[CH3:15][NH:16][C:4]([C:6]1[CH:11]=[C:10]([Cl:12])[CH:9]=[CH:8][N:7]=1)=[O:3]

Komponenten

5

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A suspension of 17.8 g (0.103 mol, 1 eq) of 4-chloro-pyridine-2-carboxylic acid methyl ester hydrochloride in 15 mL, of methanol was cooled to 0° C. and slowly treated with a 2.0 M solution of methylamine in tetrahydrofuran at a rate that kept internal temperature below 5° C. The reaction mixture was stirred at 0° C. for 2 hours, then slowly allowed to warm up to ambient temperature and stirred for 18 hours. Solvent was removed in vacuum, approx. 200 mL of ethyl acetate was added and the resulting suspension was filtered. The precipitate was washed with 100 mL of ethyl acetate. The combined ethyl acetate solutions were washed three times with 100 mL of brine and dried over sodium sulfate. Solvent was removed in vacuum to yield 14.16 g of the product as orange oil. Yield: 80.5%.

Aufarbeitung

  1. customtemperature below 5° C
  2. temperatureto warm up to ambient temperature
  3. stirringstirred for 18 hours
  4. customSolvent was removed in vacuum, approx. 200 mL of ethyl acetate
  5. additionwas added
  6. filtrationthe resulting suspension was filtered
  7. washThe precipitate was washed with 100 mL of ethyl acetate
  8. washThe combined ethyl acetate solutions were washed three times with 100 mL of brine
  9. dry with materialdried over sodium sulfate
  10. customSolvent was removed in vacuum

Quellen und Nachweise

ORD-Eintrag
ord-a4e4c8b5a6254c1f8b5c73c2e6f29149
Quelldatensatz
uspto-grants-2013_02
Patentnummer
US08372971B2

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