Dimethylamine → N,N-dimethyl-[5-(4-heptylbenzoyl)-4,5,6,7-tetrahydrofuro[3,2-c]pyridin-2-ylmethyl]amine

HRID 611135Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 611135
[CH2:1]([C:8]1[CH:24]=[CH:23][C:11]([C:12]([N:14]2[CH2:19][CH2:18][C:17]3[O:20][CH:21]=[CH:22][C:16]=3[CH2:15]2)=[O:13])=[CH:10][CH:9]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].[CH3:25][NH:26][CH3:27].[CH2:28]=O>C(O)(=O)C>[CH3:25][N:26]([CH2:28][C:21]1[O:20][C:17]2[CH2:18][CH2:19][N:14]([C:12](=[O:13])[C:11]3[CH:23]=[CH:24][C:8]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7])=[CH:9][CH:10]=3)[CH2:15][C:16]=2[CH:22]=1)[CH3:27]

Komponenten

5

Edukt 3

HCID 674DimethylamineHCID 712FormaldehydeHCID 196000045-(4-Heptylbenzoyl)-4,5,6,7-tetrahydrofuro[3,2-c]pyridine

Produkt 1

HCID 19599914N,N-dimethyl-[5-(4-heptylbenzoyl)-4,5,6,7-tetrahydrofuro[3,2-c]pyridin-2-ylmethyl]amine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

To a solution of 0.190 g (0.584 mmol) of 5-(4-heptylbenzoyl)-4,5,6,7-tetrahydrofuro[3,2-c]pyridine in 20 ml of acetic acid, 0.079 ml (0.88 mmol) of 50% aqueous dimethylamine and 0.071 ml (0.88 mmol) of 37% aqueous formaldehyde were added, followed by stirring at 100° C. for 50 minutes. After the solvent was distilled off under reduced pressure, the residual solution was alkalified with 5% aqueous sodium hydrogen carbonate, and extracted with dichloromethane 2 times. The combined organic layer was washed with water and dried over anhydrous sodium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (chloroform to chloroform/methanol=25/1) to yield the desired product.

Aufarbeitung

  1. distillationAfter the solvent was distilled off under reduced pressure
  2. extractionextracted with dichloromethane 2 times
  3. washThe combined organic layer was washed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. distillationthe solvent was distilled off under reduced pressure
  6. customThe resulting crude product was purified by silica gel column chromatography (chloroform to chloroform/methanol=25/1)

Quellen und Nachweise

ORD-Eintrag
ord-0fefda61872640d89a984bdfb1dcdbdc
Quelldatensatz
uspto-grants-1999_12
Patentnummer
US05998433

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