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HRID 416611作成日:2026年10月25日

Ethyl 2-aminothiazole-4-carboxylate → Ethyl 6-(2-nitrophenyl)imidazo[2,1-b]thiazole-3-carboxylate

https://huagongshe.com/reaction/416611

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-aminothiazole-4-carboxylateHCID 73216—
反応物2-Bromo-2'-nitroacetophenoneHCID 244025—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物Ethyl 6-(2-nitrophenyl)imidazo[2,1-b]thiazole-3-carboxylateHCID 2523252279.4%

反応手順

In a typical run, 2.1 g of ethyl 2-aminothiazole-4-carboxylate (Combi-Blocks, 0.0123 mol) was mixed with 25 mL of methyl ethyl ketone along with 2-bromo-2′-nitroacetophenone (3.0 g, 0.0123 mol). The reaction mixture was stirred under reflux for 18 hours. It was then cooled to room temperature and filtered to remove some of the solids. The filtrate was concentrated to afford 3.10 g of 6-(2-nitro-phenyl)-imidazo[2,1-b]thiazole-3-carboxylic acid ethyl ester (MS, M++H=318).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088928B2
出典データセットuspto-grants-2012_01
ORD IDord-f11f0e9818664a20991016afb4914dc7
出典メモuspto-grants-2012_01