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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279385Erstellt: 24. Oktober 2026

Methanol → 2-Chloro-4-hydrazinyl-5-methoxypyrimidine

https://huagongshe.com/de/reaction/279385

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktHydrazineHCID 9321—
EduktSodium CarbonateHCID 10340—
Edukt2,4-Dichloro-5-methoxypyrimidineHCID 601401—
LösungsmittelTolueneHCID 1140—
Produkt2-Chloro-4-hydrazinyl-5-methoxypyrimidineHCID 1141266686%

Reaktionsbedingungen

Temperatur42 °C

Reaktionsschritte

Anhydrous sodium carbonate (5.83 g, 0.055 mole), methanol (60 mL), and 35% aqueous hydrazine (11.0 g, 0.120 mole) were loaded into a 500 mL three necked flask equipped with a thermometer, magnetic stirrer, condenser, and addition funnel. A solution/partial slurry of 2,4-dichloro-5-methoxy-pyrimidine (17.91 g, 0.100 mole) in toluene (30 mL) was added dropwise over 39 min. During the addition, the reaction temperature rose from 15° C. to 39° C. and the solids dissolved to form a clear, pale yellow solution. The reaction mixture was heated to 42° C. for 4.1 h, after which the heat source was removed. Slow, dropwise addition of water (180 mL), caused the product to crystallize out of solution. The resulting slurry was stirred for 2 h at room temperature, then the product was recovered by filtration through Whatman #1 filter paper using a Buchner funnel and aspirator vacuum. After washing the filter cake with water, the product was dried overnight in vacuo at 40° C., to give 15.02 g of white 2-chloro-4-hydrazino-5-methoxypyrimidine (purity 96.2%, yield=82.8%): 1H NMR (300 MHz, DMSO-d6) 3.33 (s, 3H), 3.78 (s, 3H), 4.39 (br s, 2H), 7.59 (s, 1H), 8.73 (br s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06362335B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-3ea2a7f9199d428ea3496179c602b3b4
Quellennotizuspto-grants-2002_03