戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2424372作成日:2026年10月27日

2-Aminobenzenesulfonamide → 2-(5-Bromo-2-chloropyrimidin-4-ylamino)benzenesulfonamide

https://huagongshe.com/reaction/2424372

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminobenzenesulfonamideHCID 72894—
反応物5-Bromo-2,4-dichloropyrimidineHCID 289973—
反応物Sodium BicarbonateHCID 516892—
溶媒Hydrochloric AcidHCID 313—
溶媒IsopropanolHCID 3776—
生成物2-(5-Bromo-2-chloropyrimidin-4-ylamino)benzenesulfonamideHCID 85997992—

反応条件

温度90 °C

反応手順

To a solution of 5-bromo-2,4-dichloropyrimidine (300 mg, 1.32 mmol) and 2-amino-benzenesulfonamide (340 mg, 1.97 mmol) in 2-propanol (3 mL), concentrated hydrochloric acid (0.06 mL) is added and the mixture is stirred at 90° C. for 4.5 hours. The mixture is poured into aqueous sodium hydrogen carbonate and extracted with ethyl acetate three times. The organic layer is washed with water, dried over sodium sulfate, and evaporated in vacuo. The residue is purified by column chromatography (hexane:ethyl acetate=2:1) to afford the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07964592B2
出典データセットuspto-grants-2011_06
ORD IDord-9ba9abeff4444547803d41d037ddf6a7
出典メモuspto-grants-2011_06