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HRID 30415作成日:2026年10月23日

Diethyl Ether → L-tartrate salt-1-(2-fluoro-phenyl)-3-(piperidin-4-yloxy)-1H-indazole L-tartrate

https://huagongshe.com/ja/reaction/30415

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Sodium CarbonateHCID 10340—
反応物L-Tartaric acidHCID 444305—
反応物1-(2-Fluoro-phenyl)-3-(piperidin-4-yloxy)-1h-indazole hydrochlorideHCID 57420549—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物L-tartrate salt-1-(2-fluoro-phenyl)-3-(piperidin-4-yloxy)-1H-indazole L-tartrateHCID 131727052124.9%

反応手順

A mixture of 1-(2-fluoro-phenyl)-3-(piperidin-4-yloxy)-1H-indazole hydrochloride (9.0 g, 0.026 moles) in tetrahydrofuran (20 ml) and water (100 ml) was stirred at room temperature for 0.5 hour as a solution formed. Sodium carbonate (15 g, 0.142 moles) was added portion-wise over a 5-minute period, followed by ether (150 ml). The mixture was shaken and the layers were separated. The aqueous layer was extracted with ether (100 ml). The combined organic layers were dried over magnesium sulfate and concentrated in vacuo to a gum (8.0 g, 99% crude). To this gum was added, all at once, a solution of L-tartaric acid (4.0 g, 0.0267 mol) in water (80 ml). The mixture was stirred for ˜2 minutes when a complete solution formed. Stirring was continued and after ˜2 minutes solid began precipitating. The suspension was stirred at 0° C. for 3 hours and filtered. The solid was rinsed with water (15 ml) and pressed dry under suction. Further drying in vacuo at 50° C. for 16 hours provided 10.2 g (85.5%) of the L-tartrate salt—1-(2-fluoro-phenyl)-3-(piperidin-4-yloxy)-1H-indazole L-tartrate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423054B2
出典データセットuspto-grants-2008_09
ORD IDord-ec8a8af7f4054d599a8a1236ba950fd0
出典メモuspto-grants-2008_09