Thionyl Chloride → 3-Ethyl-pentanoic acid (2,6-dimethyl-4-morpholin-4-yl-phenyl)-amide

HRID 1783368

Reaktionsgleichung

Reaktionsgleichung von HRID 1783368
[CH2:1]([CH:3]([CH2:8][CH3:9])[CH2:4][C:5]([OH:7])=O)[CH3:2].S(Cl)(Cl)=O.[CH3:14][C:15]1[CH:20]=[C:19]([N:21]2[CH2:26][CH2:25][O:24][CH2:23][CH2:22]2)[CH:18]=[C:17]([CH3:27])[C:16]=1[NH2:28].C(=O)(O)[O-].[Na+].[Cl-].[Na+].O.O>C(#N)C>[CH3:14][C:15]1[CH:20]=[C:19]([N:21]2[CH2:26][CH2:25][O:24][CH2:23][CH2:22]2)[CH:18]=[C:17]([CH3:27])[C:16]=1[NH:28][C:5](=[O:7])[CH2:4][CH:3]([CH2:1][CH3:2])[CH2:8][CH3:9]

Komponenten

6

Edukt 4

HCID 24386Thionyl ChlorideHCID 1344603-Ethylpentanoic acidHCID 230094142,6-Dimethyl-4-morpholin-4-yl-phenylamineHCID 131727349Sodium bicarbonate brine water

Produkt 1

HCID 116668733-Ethyl-pentanoic acid (2,6-dimethyl-4-morpholin-4-yl-phenyl)-amideAusbeute 30,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel2×

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

3-Ethylpentanoic acid (0.79 g) and thionyl chloride (0.44 mL) were mixed-in acetonitrile (10 mL) and heated to 110° C. for 5 minutes in a sealed microwave process vial. 2,6-Dimethyl-4-morpholin-4-yl-phenylamine (1:25 g) dissolved in acetonitrile (10 mL) was added to the reaction mixture and heated to 150° C. for 15 minutes in a sealed microwave process vial. Saturated aqueous sodium bicarbonate/brine/water (1:1:1, 50 mL) was added to the crude mixture and it was extracted with ethyl acetate (3×50 mL). The combined organic phases were dried over magnesium sulfate and concentrated in vacuo. The crude product was recrystallized from hot toluene, and the product was collected by filtration, washed with cold toluene and dried in vacuo to furnish 0.59 g (30% yield) of the title compound as an off-white solid. LC-MS (m/z) 319 (MH+); tR=2.04, (UV, ELSD) 98%, 99%. 1H NMR (500 MHz, DMSO-d6): 0.87 (t, 6H), 1.35 (qui, 4H), 1.76 (m, 1H), 2.07 (s, 6H), 2.20 (d, 2H), 3.05 (t, 4H), 3.71 (t, 4H), 6.62 (s, 2H), 8.94 (s, 1H).

Aufarbeitung

  1. additionwas added to the reaction mixture
  2. temperatureheated to 150° C. for 15 minutes in a sealed microwave process vial
  3. extractionwas extracted with ethyl acetate (3×50 mL)
  4. dry with materialThe combined organic phases were dried over magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe crude product was recrystallized from hot toluene
  7. filtrationthe product was collected by filtration
  8. washwashed with cold toluene
  9. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-5211cc71422745739d3aa7d204c09c02
Quelldatensatz
uspto-grants-2009_03
Patentnummer
US07501414B2

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