Ethanolamine → 3-[3-(5-Fluoro-pyridin-2-yl)-5-methyl-isoxazol-4-ylmethoxy]-isothiazole-5-carboxylic acid (2-hydroxy-ethyl)-amide

HRID 1920939Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1920939
CO[C:3]([C:5]1[S:9][N:8]=[C:7]([O:10][CH2:11][C:12]2[C:13]([C:18]3[CH:23]=[CH:22][C:21]([F:24])=[CH:20][N:19]=3)=[N:14][O:15][C:16]=2[CH3:17])[CH:6]=1)=[O:4].[CH2:25]([CH2:27][NH2:28])[OH:26]>>[CH:13]([NH2:14])([CH3:18])[CH3:12].[OH:26][CH2:25][CH2:27][NH:28][C:3]([C:5]1[S:9][N:8]=[C:7]([O:10][CH2:11][C:12]2[C:13]([C:18]3[CH:23]=[CH:22][C:21]([F:24])=[CH:20][N:19]=3)=[N:14][O:15][C:16]=2[CH3:17])[CH:6]=1)=[O:4]

Komponenten

4

Versuchsvorschrift

As described for example 38b, 3-[3-(5-fluoro-pyridin-2-yl)-5-methyl-isoxazol-4-ylmethoxy]-isothiazole-5-carboxylic acid methyl ester (120 mg, 0.34 mmol), was converted, using ethanolamine (25 mg, 0.41 mmol), instead of isopropyl amine, to the title compound (91 mg, 70%) which was obtained as a white solid after purification by chromatography (silica, dichloromethane:methanol=97.5:2.5 to 9:1). MS: m/e=379.3 [M+H]+.

Quellen und Nachweise

ORD-Eintrag
ord-8628b06608a5438584709a8d22af3f8d
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08173652B2

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