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2,5-Dihydroxybenzoic acid → HCID 11508769, Verbindung

HRID 2373327
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2373327
[OH:1][C:2]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH3:12][NH:13][C@H:14]([CH2:16]/[CH:17]=[CH:18]/[C:19]1[CH:20]=[N:21][CH:22]=[C:23]([O:25][CH3:26])[CH:24]=1)[CH3:15].C(OCC)(=O)C>C(O)C>[OH:1][C:2]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH3:12][NH:13][C@H:14]([CH2:16]/[CH:17]=[CH:18]/[C:19]1[CH:20]=[N:21][CH:22]=[C:23]([O:25][CH3:26])[CH:24]=1)[CH3:15]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 34692,5-Dihydroxybenzoic acidHCID 8857Ethyl AcetateHCID 102624065-(5-Methoxy-3-pyridinyl)-N-methyl-4-penten-2-amine, (2S,4E)-

Produkt 1

HCID 11508769HCID 11508769, VerbindungAusbeute 91 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel3×

Versuchsvorschrift

A hot solution of 2,5-dihydroxybenzoic acid (gentisic acid) (0.582 g, 3.78 mmol) in absolute ethanol (1 mL) was added to a warm solution of (2S)-(4E)-N-methyl-5-(5-methoxy-3-pyridinyl)-4-penten-2-amine (1.00 g, 4.85 mmol, 86.7% E isomer by GC-FID) in absolute ethanol (1 mL), using additional ethanol (2 mL) in the transfer. The resulting mixture was concentrated via rotary evaporation, leaving 1.5 mL of ethanol in the solution. With stirring and heating to near reflux, crystallization occurred. The resulting hot mixture was treated drop-wise with ethyl acetate (5.5 mL). After cooling to room temperature, the mixture was further cooled at 5° C. for 48 h. The resulting solids were filtered, washed with ethyl acetate (2×5 mL) and dried at 50° C. to give 1.24 g (91%) of an off-white powder (98.0% E isomer by GC-FID for the free base). To remove the color from the sample, the material was recrystallized from ethanol/isopropanol (3.5 mL:5.5 mL) to give 1.03 g (83% recovery) of an off-white powder and subsequently recrystallized from ethanol/ethyl acetate (3 mL:12 mL) to give 0.90 g (87% recovery) of a white, crystalline powder, mp 166-167° C.

Aufarbeitung

  1. concentrationThe resulting mixture was concentrated via rotary evaporation
  2. customleaving 1.5 mL of ethanol in the solution
  3. temperatureheating to near reflux, crystallization
  4. temperaturethe mixture was further cooled at 5° C. for 48 h
  5. filtrationThe resulting solids were filtered
  6. washwashed with ethyl acetate (2×5 mL)
  7. customdried at 50° C.

Quellen und Nachweise

ORD-Eintrag
ord-dacd4a9efac8448199f58c9bb7281bdc
Quelldatensatz
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07459469B2

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