Hydrochloric Acid → 4-Sec-butyl-1,2-dihydro-6-methyl-2-oxopyridine-3-carbonitrile

HRID 1476509Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1476509
CC([O-])(C)C.[K+].[C:7]([CH2:9][C:10]([NH2:12])=[O:11])#[N:8].[CH3:13][CH:14]([CH2:20][CH3:21])/[CH:15]=[CH:16]/[C:17](=O)[CH3:18].O=O.Cl>CS(C)=O.O>[CH:14]([C:15]1[CH:16]=[C:17]([CH3:18])[NH:12][C:10](=[O:11])[C:9]=1[C:7]#[N:8])([CH2:20][CH3:21])[CH3:13]

Komponenten

8

Edukt 5

HCID 313Hydrochloric AcidHCID 977OxygenHCID 7898CyanoacetamideHCID 53645545-Methyl-3-hepten-2-oneHCID 23665647Potassium tert-butoxide2×

Produkt 1

HCID 682102564-Sec-butyl-1,2-dihydro-6-methyl-2-oxopyridine-3-carbonitrileAusbeute 53 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 679Dimethyl SulfoxideLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

To a stirred solution of t-BuOK (8 g, 71.42 mmol) and cyanoacetamide (6.6 g, 78.57 mmol) in DMSO (80 mL) was added (E)-5-methylhept-3-en-2-one, 2 (9 g, 71.42 mmol) under argon atmosphere at room temperature. The reaction mixture was stirred at room temperature for 1 h and then added additional t-BuOK (24 g, 214.28 mmol) was added. Then argon was displaced by oxygen and stirred at RT for 48 h. The reaction mixture was cooled to 0° C., diluted with water (36 mL) followed by 4N HCl (up to pH˜4) and the resulting reaction mixture was stirred for 15 min. The separated solid was collected by filtration, washed with water (10 mL), pet ether (100 mL) and dried to afford the title compound as yellow solid (7 g, 53%). 1H NMR (DMSO-d6, 400 MHz): δ 0.816-0.779 (t, 3H, J=7.6 Hz), 1.178-1.161 (d, 3H, J=6.8 Hz), 1637-1.505 (m, 2H), 2.24 (s, 3H), 2.814-2.760 (m, 1H), 6.239 (s, 1H), 12.324 (bs, 1H); LCMS (ES−) m/z=189.20 (M−H)

Aufarbeitung

  1. additionwas added
  2. stirringstirred at RT for 48 h
  3. temperatureThe reaction mixture was cooled to 0° C.
  4. customthe resulting reaction mixture
  5. stirringwas stirred for 15 min
  6. filtrationThe separated solid was collected by filtration
  7. washwashed with water (10 mL), pet ether (100 mL)
  8. customdried

Quellen und Nachweise

ORD-Eintrag
ord-edc9f152105740a49e9e34992d0c9631
Quelldatensatz
uspto-grants-2015_04
Patentnummer
US09018382B2

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