Sodium Hydroxide → HCID 71087699, Verbindung

HRID 2405082Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2405082
[CH2:1]([N:3]1[C:11]2[CH:10]=[C:9]([C:12]([O:14]C)=[O:13])[N:8]=[CH:7][C:6]=2[C:5]([CH3:16])=[CH:4]1)[CH3:2].[OH-].[Na+]>C1COCC1>[CH2:1]([N:3]1[C:11]2[CH:10]=[C:9]([C:12]([OH:14])=[O:13])[N:8]=[CH:7][C:6]=2[C:5]([CH3:16])=[CH:4]1)[CH3:2]

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 71087757HCID 71087757, Verbindung

Produkt 1

HCID 71087699HCID 71087699, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

In a 200-ml round bottom flask, methyl 1-ethyl-3-methyl-1H-pyrrolo[3,2-c]pyridine-6-carboxylate (1N, 6.0 g, 28 mmol) was dissolved in THF (50 ml). To the mixture was added a 2M NaOH (28 ml, 55 mmol) solution. The reaction was stirred at room temperature for 3 hrs. After completion, volatiles were removed and the residue was cooled in an ice bath and neutralized with dilute HCl to pH=4.0-4.5. The aqueous mixture washed with ethyl acetate (2×100 ml) and then lyophilized to give the crude product 1-ethyl-3-methyl-1H-pyrrolo[3,2-c]pyridine-6-carboxylic acid (1O) which is used in the next step without further purification.

Aufarbeitung

  1. customAfter completion, volatiles were removed
  2. temperaturethe residue was cooled in an ice bath
  3. washThe aqueous mixture washed with ethyl acetate (2×100 ml)

Quellen und Nachweise

ORD-Eintrag
ord-cd24699dac754b34880ab939ae009daf
Quelldatensatz
uspto-grants-2014_08
Patentnummer
US08802695B2

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