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HRID 619063作成日:2026年10月25日

Hydrochloric Acid → N-[4-(2-fluoro-5-trifluoromethyl-phenyl)-thiazol-2-yl]-4-methoxy-benzenesulfonamide

https://huagongshe.com/reaction/619063

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-Methoxybenzenesulfonyl chlorideHCID 7401—
反応物4-(2-Fluoro-5-trifluoromethyl-phenyl)-thiazol-2-ylamine hydrobromideHCID 21845595—
溶媒PyridineHCID 1049—
生成物N-[4-(2-fluoro-5-trifluoromethyl-phenyl)-thiazol-2-yl]-4-methoxy-benzenesulfonamideHCID 2184557341.3%

反応手順

A mixture of 0.5 g of 4-(2-fluoro-5-trifluoromethyl-phenyl)-thiazol-2-ylamine hydrobromide with 0.33 g of 4-methoxy-benzenesulfonyl chloride was stirred overnight with 2 ml of pyridine. The resulting, red colored suspension was poured into 30 ml of 1N hydrochloric acid and the mixture was extracted lo with ethyl acetate. The organic phase was dried with magnesium sulphate and concentrated. The residue was dissolved in a mixture of 30 ml of ethanol and 20 ml of 2N sodium hydroxide solution. After the addition of 0.5 g of active charcoal the mixture was stirred at room temperature for 30 minutes and subsequently the active charcoal was filtered off. The product separated upon neutralization with concentrated hydrochloric acid. Recrystallization from 30 ml of 50% ethanol yielded 0.26 g of N-[4-(2-fluoro-5-trifluoromethyl-phenyl)-thiazol-2-yl]-4-methoxy-benzenesulfonamide as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05958910
出典データセットuspto-grants-1999_09
ORD IDord-fbb3c4e2f5e44399b93db1bf2ee32789
出典メモuspto-grants-1999_09