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HRID 1741作成日:2026年10月23日

N-((7-chloro-3-hydroxy-6-(2,2,2-trifluoroethyloxy)quinolin-2-yl)carbonyl)glycine → N-((3-Hydroxy-6-((2,2,2-trifluoroethyl)oxy)quinolin-2-yl)carbonyl)glycine hydrochloride

https://huagongshe.com/ja/reaction/1741

反応式

関与物質

役割名称HCID仕込み量
反応物N-((7-chloro-3-hydroxy-6-(2,2,2-trifluoroethyloxy)quinolin-2-yl)carbonyl)glycineHCID 19692257—
溶媒Formic AcidHCID 284—
生成物N-((3-Hydroxy-6-((2,2,2-trifluoroethyl)oxy)quinolin-2-yl)carbonyl)glycine hydrochlorideHCID 19692270—

反応手順

0.5 g (1.3 mmol) of N-((7-chloro-3-hydroxy-6-(2,2,2-trifluoroethyloxy)quinolin-2-yl)carbonyl)glycine (title compound from Example 31) was dissolved in 26 ml of methanolic formic acid (4.4% strength), and a further 26 ml of methanolic formic acid were added at 20° C. After addition of 0.5 g of Pd/C (10%), the mixture was stirred at 20° C. for 1 hour, the catalyst was filtered off, the filtrate was concentrated and the residue was crystallized with diisopropyl ether. 250 mg of product were obtained, melting point>300° C. (sintering at 207° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726305
出典データセットuspto-grants-1998_03
ORD IDord-29db157c047e49c9aec1fa6bbd5e3bdc
出典メモuspto-grants-1998_03