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HRID 398273作成日:2026年10月26日

Water → 5-Chloro-N-[(S)-2-hydroxy-1-(4-hydroxycyclohexyl)ethyl]thiophene-2-sulfonamide

https://huagongshe.com/reaction/398273

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物N-(4-Hydroxyphenyl)glycineHCID 67149—
反応物5-Chlorothiophene-2-sulfonyl chlorideHCID 2733925—
反応物HCID 178418361HCID 178418361—
触媒NickelHCID 935—
溶媒Sodium HydroxideHCID 14798—
生成物5-Chloro-N-[(S)-2-hydroxy-1-(4-hydroxycyclohexyl)ethyl]thiophene-2-sulfonamideHCID 59086185—

反応条件

温度0 °C

反応手順

To a solution of 4-hydroxy-L-phenylglycine (10 g, 60 mmole) in NaOH (20 mL, 3M) was added water (380 mL) and Raney nickel (30 g). The reaction mixture was hydrogenated at about 3 atm at 60 to 80° C. for 36 h in a hydrogen bomb. The reaction mixture was filtered through Celite and reduced in volume to about 80-100 mL and dioxane (100 mL) was added. The resulting mixture was cooled to 0° C. and treated with Et3N (10 mL) and 5-chlorothiophene-2-sulfonyl chloride (16 g, 72 mmoles). The reaction was allowed to warm up to 25° C. and stirred overnight. The dioxane and Et3N were removed and the remaining aqueous solution diluted with 1N aq. HCl. The resulting precipitate was collected, washed with water and diethyl ether to give the desired product as a white solid (12 g, 50% in two steps) (100% purity by ELSD, m/z=352 (M−1)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06610734B2
出典データセットuspto-grants-2003_08
ORD IDord-14d8f51c5c6e4961864a90bb7cf32a45
出典メモuspto-grants-2003_08