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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231405Erstellt: 25. Oktober 2026

2-Amino-4,6-dimethoxypyrimidine → 4-(Cyclopropylcarbonyl)-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-1-methyl-1H-pyrazole-5-sulfonamide

https://huagongshe.com/reaction/231405

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-4,6-dimethoxypyrimidineHCID 118946—
Edukt4-Cyclopropylcarbonyl-1-methyl-5-pyrazolesulfonamideHCID 14230998—
EduktPhenylcarbamateHCID 21896570—
EduktHCID 22171225HCID 22171225—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-(Cyclopropylcarbonyl)-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-1-methyl-1H-pyrazole-5-sulfonamideHCID 14230999—

Reaktionsschritte

To a stirring mixture of the sulfonamide from Example 2 (175 mg, 0.76 mmol) and the phenylcarbamate of 4,6-dimethoxy-2-aminopyrimidine (210 mg, 0.76 mmol) in 3 ml of acetonitrile was added diazobicycloundecane (116 mg, 0.76 mmol). The solution was stirred for approximately 10 minutes. Acidification of the reaction mixture and filtration of the resulting solids afforded 300 mg of the desired compound m.p. 189°-192° C. NMR (200 MHz, CDCl3) 1.0 (m, 2H), 1.1 (m, 2H), 2.4 (m, 1H), 4.0 (s, 6H), 4.35 (s, 1H), 5.80 (s, 1H), 7.4 (br. s, 1H), 8.05 (s, 1H), 12.9 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04846878
Quelldatensatzuspto-grants-1989_07
ORD IDord-5b8f307d02064ce6995a15186cec2310
Quellennotizuspto-grants-1989_07