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HRID 559828作成日:2026年10月26日

2-Aminothiazole → 2-[([[(2-Phenoxyanilino)sulfonyl]amino]carbonyl)amino]thiazole

https://huagongshe.com/reaction/559828

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminothiazoleHCID 2155—
反応物Chlorosulfonyl isocyanateHCID 70918—
反応物Benzenamine, 2-phenoxy-HCID 75899—
反応物DiisopropylethylamineHCID 81531—
溶媒TetrahydrofuranHCID 8028—
生成物2-[([[(2-Phenoxyanilino)sulfonyl]amino]carbonyl)amino]thiazoleHCID 5973284566.6%

反応条件

温度0 °C

反応手順

To a solution of chlorosulfonyl isocyanate (0.22 ml, 2.5 mmol) in tetrahydrofuran (25 ml) were added 2-phenoxyaniline (0.37 g, 2.0 mmol) and DIEA (0.89 ml, 5.0 mmol) at −78° C. The solution was stirred and slowly allowed to warmed up to 0° C. To this reaction mixture, was added 2-amino thiazole (0.20 g, 2.0 mmol) and continued stirring at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure and the crude product was purified by column chromatography (ethylacetate:hexanes, from 50:50 to 90:10 as eluent system) to afford the title compound (0.52 g, 66%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063081B2
出典データセットuspto-grants-2011_11
ORD IDord-2767f934212a479eb68a8f532e7dca4c
出典メモuspto-grants-2011_11