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HRID 619044作成日:2026年10月27日

Hydrochloric Acid → 5-tert-Butyl-thiophene-2-sulfonic acid [4-(3-nitro-phenyl)-thiazol-2-yl]-amide

https://huagongshe.com/reaction/619044

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-(3-Nitro-phenyl)-thiazol-2-ylamine hydrobromideHCID 2870445—
反応物5-Tert-butylthiophene-2-sulfonyl chlorideHCID 21845564—
溶媒PyridineHCID 1049—
生成物5-tert-Butyl-thiophene-2-sulfonic acid [4-(3-nitro-phenyl)-thiazol-2-yl]-amideHCID 86753755—

反応手順

A mixture of 0.5 g of 4-(3-nitro-phenyl)-thiazol-2-ylamine hydrobromide with 0.43 g of 5-tert-butyl-thiophene-2-sulfonyl 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 three times with 30 ml of ethyl acetate each time. The organic phases were combined, dried with magnesium sulphate and the solvent was removed on a rotary evaporator. The residue was chromatographed on 50 g of Kieselgel 60 with ethyl acetate/hexane (1:2) as the eluent. The product-containing fractions were concentrated and the residue was dissolved in a mixture of 20 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. 0.20 g of 5-tert-butyl-thiophene-2-sulfonic acid [4-(3-nitro-phenyl)-thiazol-2-yl]-amide separated as yellowish crystals after neutralization with concentrated hydrochloric acid and repeated boiling.

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-ce3afca5fad3405fa923234338b859db
出典メモuspto-grants-1999_09