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HRID 1884821作成日:2026年10月24日

Sulfamethazine → 4-Benzylamino-N-(4,6-dimethylpyrimidin-2-yl)-benzenesulfonamide

https://huagongshe.com/ja/reaction/1884821

反応式

関与物質

役割名称HCID仕込み量
反応物SulfamethazineHCID 5327—
反応物Benzyl BromideHCID 7498—
反応物Cesium carbonateHCID 10796—
溶媒MethanolHCID 887—
生成物4-Benzylamino-N-(4,6-dimethylpyrimidin-2-yl)-benzenesulfonamideHCID 10155893—

反応手順

100 mg (0.36 mmol) sulfamethazine and 70.8 μl (0.60 mmol) benzyl bromide were dissolved in 4 ml methanol. Caesium carbonate (113.4 mg, 0.35 mmol) was added and solution was refluxed overnight with stirring. The reaction mixture was then evaporated to dryness, and purified on silica using gradient elution (chloroform to 2% methanol in chloroform) to obtain white crystals in a yield similar to that described in example 1 for step III. 1H NMR (CDCl3, 500 MHz): 7.93 (2H, m), 7.31 (5H, m), 6.58 (3H, m), 4.36 (2H, s), 2.34 (6H, s); MS (ESI+): m/z 369 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06767909B2
出典データセットuspto-grants-2004_07
ORD IDord-cbdbf0c9d743492b9dc28d251d1b0053
出典メモuspto-grants-2004_07