Lithium hydroxide, monohydrate → 5-[3-(4-Fluoro-phenyl)-5-methyl-3H-[1,2,3]triazol-4-ylmethoxy]-pyrazine-2-carboxylic acid

HRID 402456Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 402456
O.[OH-].[Li+].C[O:5][C:6]([C:8]1[CH:13]=[N:12][C:11]([O:14][CH2:15][C:16]2[N:17]([C:22]3[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=3)[N:18]=[N:19][C:20]=2[CH3:21])=[CH:10][N:9]=1)=[O:7]>O.C1COCC1>[F:28][C:25]1[CH:24]=[CH:23][C:22]([N:17]2[C:16]([CH2:15][O:14][C:11]3[N:12]=[CH:13][C:8]([C:6]([OH:7])=[O:5])=[N:9][CH:10]=3)=[C:20]([CH3:21])[N:19]=[N:18]2)=[CH:27][CH:26]=1

Komponenten

5

Versuchsvorschrift

A solution of lithium hydroxide monohydrate (180 mg, 4.25 mmol) in water (7.3 mL) was added dropwise to a suspension of 5-[3-(4-fluoro-phenyl)-5-methyl-3H-[1,2,3]triazol-4-ylmethoxy]-pyrazine-2-carboxylic acid methyl ester (730 mg, 2.13 mmol) in THF (7.3 mL). The reaction mixture was then stirred at room temperature for 30 min and was then evaporated and the residue dissolved in water, acidified with HCl (1N), and the resulting precipitate filtered off to afford the title product (700 mg, 100%) as a white solid. MS: m/e=330.1 [M−H]−.

Aufarbeitung

  1. customwas then evaporated
  2. dissolutionthe residue dissolved in water
  3. filtrationthe resulting precipitate filtered off

Quellen und Nachweise

ORD-Eintrag
ord-35dc9735a7f24ebe9153ea890e7c7cef
Quelldatensatz
uspto-grants-2014_06
Patentnummer
US08742097B2

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