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HRID 30334作成日:2026年10月26日

Trichloroacetyl isocyanate → Methyl 5-(4-methoxyphenyl)-2-({[(trichloroacetyl)amino]carbonyl}amino)thiophene-3-carboxylate

https://huagongshe.com/reaction/30334

反応式

関与物質

役割名称HCID仕込み量
反応物Trichloroacetyl isocyanateHCID 76400—
反応物2-Amino-5-(4-methoxy-phenyl)-thiophene-3-carboxylic acid methyl esterHCID 68963567—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 5-(4-methoxyphenyl)-2-({[(trichloroacetyl)amino]carbonyl}amino)thiophene-3-carboxylateHCID 11546916—

反応手順

To a stirred solution of 2-Amino-5-(4-methoxy-phenyl)-thiophene-3-carboxylic acid methyl ester (7.15 g, 27.2 mmol) in anhydrous THF (150 mL) was added trichloroacetyl isocyanate (6.4 mL, 54 mmol) slowly over a period of 5 min. After the addition was complete, a precipitate formed and the reaction stirred for an additional 1 h. The desired product was obtained by filtration to give 6.9 g (56%) an off-white solid. The product was used in the next step without purification 1H NMR (d6-DMSO δ 12.3, br s, 1H; δ 12.2, s, 1H; δ 7.46, d, 2H; δ 7.32, s, 1H; δ 6.85, d, 2H; δ 3.75, s, 3H; δ 3.66, s, 3H), LC/MS (APCI, ES, M+H=451).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423061B2
出典データセットuspto-grants-2008_09
ORD IDord-4c864b855fd644c992f4f26b7ed6bdd3
出典メモuspto-grants-2008_09