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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1884823Erstellt: 27. Oktober 2026

Sulfamethazine → N-[4-(4,6-Dimethylpyrimidin-2-ylsulfamoyl)-phenyl]-2-(2-methoxyphenyl)-acetamide

https://huagongshe.com/reaction/1884823

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfamethazineHCID 5327—
Edukt2-Methoxyphenylacetic acidHCID 7134—
EduktTriethylamineHCID 8471—
EduktDiisopropylcarbodiimideHCID 12734—
LösungsmittelChloroformHCID 6212—
ProduktN-[4-(4,6-Dimethylpyrimidin-2-ylsulfamoyl)-phenyl]-2-(2-methoxyphenyl)-acetamideHCID 2350490040%

Reaktionsschritte

2-Methoxyphenylacetic acid (33 mg, 0.20 mmol) and sulfamethazine (55 mg, 0.20 mmol) were dissolved in 4 ml of chloroform. Triethylamine (70 μl, 0.55 mmol) and diisopropylcarbodiimide (50 μl, 0.20 mmol) were added to the reaction mixture. Solution was stirred and refluxed overnight. The reaction mixture was then evaporated to dryness, washed with water and purified on silica using gradient elution (chloroform to 2% methanol in chloroform) to obtain white crystals with the yield of 40%. 1H NMR (CDCl3, 500 MHz): 8.04 (2H, m), 7.54 (2H, m), 7.30 (2H, m), 6.98 (2H, m), 6.60 (1H, s), 3.95 (3H, s), 3.72 (2H, s), 2.33 (6H, s); MS (ESI+): m/z 449 (M+Na)+, 427 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06767909B2
Quelldatensatzuspto-grants-2004_07
ORD IDord-433da962c43a4fbf8a0b104ef2722b91
Quellennotizuspto-grants-2004_07