Water → 2-(Benzylthio)-N,N-dimethylnicotinamide

HRID 414006Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 414006
CC(C)([O-])C.[K+].[CH2:7]([SH:14])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[CH3:15][N:16]([CH3:26])[C:17]([C:19]1[C:20](Cl)=[N:21][CH:22]=[CH:23][CH:24]=1)=[O:18].O>CN(C)C=O>[CH3:15][N:16]([CH3:26])[C:17]([C:19]1[C:20]([S:14][CH2:7][C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[N:21][CH:22]=[CH:23][CH:24]=1)=[O:18]

Komponenten

6

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

A solution of 25.0 g (223 mmol) of potassium t-butoxide in 100 ml of dimethylformamide was cooled to 0° C. and 22 ml (186 mmol) of benzyl mercaptan added dropwise at 0° C. After addition was complete, the reaction mixture was allowed to warm to 25° C. and stirred at this temperature for 15 minutes. The reaction mixture was then re-cooled to 0° C. and 34.0 g (186 mmol) of N,N-dimethyl-2-(chloro)-3-pyridinecarboxamide added in one portion. After an exotherm to 50° C., the mixture was heated at 80° C. for 1.5 hour. The mixture was cooled, poured into 100 ml of water and extracted with ether. The combined organic extracts were washed twice with water, then brine and dried over sodium sulfate. Concentration gave 19.2 g of a viscous yellow oil. IR (Nujol) 1640 (CONMe2) cm-1.

Aufarbeitung

  1. additionAfter addition
  2. temperatureThe reaction mixture was then re-cooled to 0° C.
  3. temperatureAfter an exotherm to 50° C., the mixture was heated at 80° C. for 1.5 hour
  4. temperatureThe mixture was cooled
  5. extractionextracted with ether
  6. washThe combined organic extracts were washed twice with water
  7. dry with materialbrine and dried over sodium sulfate
  8. concentrationConcentration

Quellen und Nachweise

ORD-Eintrag
ord-e095c60610ed4391bd00b36cd56e0f65
Quelldatensatz
uspto-grants-1988_12
Patentnummer
US04789393

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