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Sodium Hydroxide → 2-Bromo-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylic acid

HRID 874351
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 874351
[OH-].[Na+].[Br:3][C:4]1[N:16]=[C:7]2[CH:8]=[C:9]([C:12]([O:14]C)=[O:13])[CH:10]=[CH:11][N:6]2[N:5]=1>CO>[Br:3][C:4]1[N:16]=[C:7]2[CH:8]=[C:9]([C:12]([OH:14])=[O:13])[CH:10]=[CH:11][N:6]2[N:5]=1
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Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 90383439Methyl 2-bromo-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylate

Produkt 1

HCID 838249652-Bromo-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylic acidAusbeute 95,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

A 1 N sodium hydroxide aqueous solution (150 ml) was added to a methanol (150 ml) suspension of the methyl 2-bromo-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylate (10 g) obtained in (Example 3.15) <Step 2>, and the obtained mixture was then stirred for 30 minutes. Thereafter, about half of the solvent was distilled away under reduced pressure, and the residue was then adjusted to pH 4 by addition of 3 N hydrochloric acid (50 ml). The precipitated solid was collected by filtration, and was then successively washed with water (50 ml) and methyl tert-butyl ether (20 ml). The obtained solid was, subjected to azeotropy with toluene to obtain the title compound (9.0 g) in the form of a white solid.

Aufarbeitung

  1. customobtained in (Example 3.15) <Step 2>
  2. distillationThereafter, about half of the solvent was distilled away under reduced pressure
  3. additionthe residue was then adjusted to pH 4 by addition of 3 N hydrochloric acid (50 ml)
  4. filtrationThe precipitated solid was collected by filtration
  5. washwas then successively washed with water (50 ml) and methyl tert-butyl ether (20 ml)

Quellen und Nachweise

ORD-Eintrag
ord-609c08ecc4cd451782e3037b7bb5b9e3
Quelldatensatz
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08980888B2

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