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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280805Erstellt: 24. Oktober 2026

2-Amino-4-methoxy-6-methyl-1,3,5-triazine → N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(2-chloroethoxycarbonyl)benzenesulfonamide

https://huagongshe.com/de/reaction/280805

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
Edukt2-(beta-Chloroethoxycarbonyl)benzenesulfonylisocyanateHCID 13920549—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(2-chloroethoxycarbonyl)benzenesulfonamideHCID 1317669680,1%

Reaktionsschritte

To 0.7 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine in 10 ml anhydrous methylene chloride solvent was added 1.45 g 2-(β-chloroethoxycarbonyl)benzenesulfonyl isocyanate with stirring at ambient temperature. The mixture was thereafter stirred for sixteen hours. The solvent was evaporated under reduced pressure and the residue triturated with hexane and filtered to yield 1.72 g of compound which melted at 167°-170° C. The solid showed infrared absorption peaks at 1700 and 1705 cm-1, consistent for N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(2-chloroethoxycarbonyl)benzenesulfonamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04591378
Quelldatensatzuspto-grants-1986_05
ORD IDord-2bed349451c848c18105a55b4b3b9a9d
Quellennotizuspto-grants-1986_05