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HRID 1800529作成日:2026年10月26日

Propionyl chloride → N-(4-chloro-2-fluoro-5-{[2-(propanoylamino)[1,3]thiazolo[5,4-b]pyridin-5-yl]oxy}phenyl)-3-(1-cyano-1-methylethyl)benzamide

https://huagongshe.com/reaction/1800529

反応式

関与物質

役割名称HCID仕込み量
反応物Propionyl chlorideHCID 62324—
反応物N-(5-[(2-Amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-4-chloro-2-fluorophenyl}-3-(1-cyano-1-methylethyl)benzamideHCID 86646015—
溶媒PyridineHCID 1049—
溶媒Ethyl AcetateHCID 8857—
生成物N-(4-chloro-2-fluoro-5-{[2-(propanoylamino)[1,3]thiazolo[5,4-b]pyridin-5-yl]oxy}phenyl)-3-(1-cyano-1-methylethyl)benzamideHCID 5950706752%

反応手順

To a solution of N-{5-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-4-chloro-2-fluorophenyl}-3-(1-cyano-1-methylethyl)benzamide produced in Example C52(v) in pyridine (1.0 mL) was added propionyl chloride (29 μL, 0.332 mmol), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with ethyl acetate (10 mL), washed with 5% aqueous sodium hydrogen carbonate solution (10 mL) and saturated brine (10 mL), and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=70/30→0/100), and the obtained solution was concentrated under reduced pressure. The residue was crystallized from ethyl acetate/hexane to give the title compound (46.7 mg, 52%) as a colorless powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08344135B2
出典データセットuspto-grants-2013_01
ORD IDord-dbba4ed4a15a45f6a7e5d0ca27d84e0b
出典メモuspto-grants-2013_01