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HRID 455179作成日:2026年10月27日

Lithium hydroxide, monohydrate → N-[6-(3-aminophenoxy)-7-cyano-1,3-benzothiazol-2-yl]acetamide

https://huagongshe.com/reaction/455179

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium hydroxide, monohydrateHCID 168937—
反応物N-(3-{[2-(Acetylamino)-7-cyano-1,3-benzothiazol-6-yl]oxy}phenyl)-2,2,2-trifluoroacetamideHCID 86644687—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物N-[6-(3-aminophenoxy)-7-cyano-1,3-benzothiazol-2-yl]acetamideHCID 8664468638.1%

反応手順

N-(3-{[2-(Acetylamino)-7-cyano-1,3-benzothiazol-6-yl]oxy}phenyl)-2,2,2-trifluoroacetamide (6.8 g, 16.2 mmol) was dissolved in a mixed solvent of tetrahydrofuran (75 mL)/methanol (25 mL)/water (25 mL), lithium hydroxide monohydrate (1.99 g, 48.5 mmol) was added, and the mixture was stirred at room temperature for 20 hr. The reaction mixture was diluted with ethyl acetate (600 mL) and tetrahydrofuran (200 mL), washed successively with 5% aqueous sodium hydrogen carbonate solution (300 mL) and saturated brine (300 mL), and dried over anhydrous sodium sulfate. Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was suspended in N,N-dimethylformamide/ethyl acetate (1:1), and the insoluble material was collected by filtration to give the title compound (2.00 g, 38%) as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08497274B2
出典データセットuspto-grants-2013_07
ORD IDord-0bdc90c51b1e440aa85823e68eb7cc67
出典メモuspto-grants-2013_07