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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30415생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Sodium CarbonateHCID 10340—
반응물L-Tartaric acidHCID 444305—
반응물1-(2-Fluoro-phenyl)-3-(piperidin-4-yloxy)-1h-indazole hydrochlorideHCID 57420549—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물L-tartrate salt-1-(2-fluoro-phenyl)-3-(piperidin-4-yloxy)-1H-indazole L-tartrateHCID 131727052124.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423054B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-ec8a8af7f4054d599a8a1236ba950fd0
출처 메모uspto-grants-2008_09