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HRID 2163513作成日:2026年10月25日

Acetic Anhydride → 2-Bromo-4-formamidothiazole

https://huagongshe.com/reaction/2163513

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物Acetic-formic anhydrideHCID 75269—
反応物Sodium AcetateHCID 517045—
反応物2-Bromo-1,3-thiazol-4-amine--hydrogen bromide (1/1)HCID 20294041—
溶媒Formic AcidHCID 284—
溶媒PyridineHCID 1049—
生成物2-Bromo-4-formamidothiazoleHCID 2029403658%

反応条件

温度50 °C

反応手順

Acetic anhydride (100 ml) was cooled to 0° C. and treated with 98% formic acid (50 ml.). The resulting mixture was heated at 50° C. for 15 minutes then cooled to 0° C. To this solution of formic-acetic anhydride was added 4-amino-2-bromothiazole hydrobromide (26 g, 0.1 m) followed dropwise by pyridine (25 ml.). The reaction mixture was allowed to stand for 1 hour at room temperature then poured onto 20% aqueous sodium acetate solution (500 ml). The resulting crystals were removed by filtration, washed once with water (100 ml) then recrystallised from ethanol to give the 2-bromo-4-formamidothiazole (12 g, 58%). m.p. 167° C. d. (Found: C, 23.55; H, 1.6; N, 13.45. C4H3N2BrOS requires C, 23.2; H, 1.45; N, 13.5%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04134984
出典データセットuspto-grants-1979_01
ORD IDord-e70a790fb4a84e349129e891279d4390
出典メモuspto-grants-1979_01