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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 325802Erstellt: 24. Oktober 2026

Octane → N-(5-Methyl-2-propargyloxyphenylsulfonyl)-N'-(4-chloro-6-methoxypyrimidin-2-yl)-urea

https://huagongshe.com/de/reaction/325802

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOctaneHCID 356—
Edukt2-Pyrimidinamine, 4-chloro-6-methoxy-HCID 79811—
Edukt5-Methyl-2-propargyloxyphenylsulfonylisocyanateHCID 13472953—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(5-Methyl-2-propargyloxyphenylsulfonyl)-N'-(4-chloro-6-methoxypyrimidin-2-yl)-ureaHCID 13472954—

Reaktionsschritte

A solution of 9.4 g of crude 5-methyl-2-propargyloxyphenylsulfonylisocyanate in 50 ml of absolute tetrahydrofuran is added dropwise at room temperature, within 10 minutes, to a solution of 3.7 g of 2-amino-4-chloro-6-methoxy-pyrimidine and 0.1 g of 1,4-diazadicyclo[2.2.2]octane in 60 ml of absolute tetrahydrofuran, in the course of which the temperature rises slightly. The reaction solution is stirred for 18 hours at room temperature; it is then filtered, and concentrated by evaporation. The residue is crystallised from ethyl acetate to thus obtain 5.8 g of N-(5-methyl-2-propargyloxyphenylsulfonyl)-N'-(4-chloro-6-methoxy-pyrimidin-2-yl)-urea, m.p. 202°-204° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04443243
Quelldatensatzuspto-grants-1984_04
ORD IDord-d1f601befbce40ebb817445180d90ed2
Quellennotizuspto-grants-1984_04