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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 247469Erstellt: 25. Oktober 2026

2-Amino-4-methoxy-6-methyl-1,3,5-triazine → N-(3-Chloropyridazine-6-sulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea

https://huagongshe.com/reaction/247469

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
EduktN-(3-chloropyridazine-6-sulfonyl)phenylcarbamateHCID 86741701—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktN-(3-Chloropyridazine-6-sulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)ureaHCID 2127574343,3%

Reaktionsschritte

A mixture of 14.2 g of N-(3-chloropyridazine-6-sulfonyl)phenylcarbamate and 6.3 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine are refluxed for 1 hour in 120 ml of absolute dioxan. When the reaction is complete, the mixture is concentrated in vacuo and the residue is taken up in a saturated aqueous solution of sodium bicarbonate and the insoluble constituents are extracted with methylene chloride. The aqueous phase is acidified with dilute hydrochloric acid and extracted with methylene chloride. The methylene chloride solution is dried over sodium sulfate and concentrated, affording 7 g of the compound of the above formula with a melting point of 135° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04707551
Quelldatensatzuspto-grants-1987_11
ORD IDord-cc3cf87295054356b17909d3b9a248d0
Quellennotizuspto-grants-1987_11