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HRID 1417270作成日:2026年10月27日

Hydrochloric Acid → 4-Methyl-N-[4-(2-nitro-phenyl)-thiazol-2-yl]-benzenesulfonamide

https://huagongshe.com/reaction/1417270

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-Toluenesulfonyl chlorideHCID 7397—
反応物4-(2-Nitro-phenyl)-thiazol-2-ylamine hydrobromideHCID 21845592—
溶媒PyridineHCID 1049—
生成物4-Methyl-N-[4-(2-nitro-phenyl)-thiazol-2-yl]-benzenesulfonamideHCID 21845599—

反応手順

A mixture of 0.5 g of 4-(2-nitro-phenyl)-thiazol-2-ylamine hydrobromide with 0.47 g of p-toluenesulfonyl chloride was stirred overnight with 2 ml of pyridine. The resulting, red colored suspension was poured into 30 ml of 1N hydrochloric acid and extracted twice with 40 ml of ethyl acetate each time. The organic extracts were combined, 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 0.4 g of active charcoal the mixture was stirred at room temperature for 30 minutes and subsequently the active charcoal was filtered off. After neutralization with concentrated hydrochloric acid and boiling there separated, upon cooling, 0.58 g of 4-methyl-N-[4-(2-nitro-phenyl)-thiazol-2-yl]-benzenesulfonamide as yellow crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05877193
出典データセットuspto-grants-1999_03
ORD IDord-e3563b45dbd14165bc552a49d9cabeae
出典メモuspto-grants-1999_03