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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2416635Erstellt: 24. Oktober 2026

Acetic Anhydride → HCID 10109395, Verbindung

https://huagongshe.com/de/reaction/2416635

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt4-[3-(4-Chlorophenyl)-2,1-benzisoxazol-5-yl]pyrimidin-2-amineHCID 2765355—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
ProduktHCID 10109395HCID 1010939530%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a suspension of 4-[3-(4-chlorophenyl)-benzo[c]isoxazol-5-yl]-pyrimidin-2-ylamine in toluene (1.5 mL) at room temperature, was added acetic anhydride (0.5 mL). The mixture was heated at 100° C. for 3 hours. The reaction mixture was diluted with water (6 mL) and the precipitate filtered then washed with toluene (2×6 mL). Purification was achieved by silica gel chromatography (4:1 ethyl acetate/hexane then 2% methanol/dichloromethane), followed by a 5% aqueous sodium bicarbonate wash (1×50 mL) to give the title compound as a yellow solid (12 mg, 30% yield). 1H NMR (500 MHz, d6-DMSO) δ 10.62 (s, 1H), 8.85 (s, 1H), 8.75 (d, 1H), 8.31 (d, 1H), 8.25 (d, 2H), 8.02 (d, 1H), 7.85 (d, 1H), 7.75 (d, 2H), 2.3 (s, 3H) ppm. LC-MS (ES+) m/e=365.13 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06825190B2
Quelldatensatzuspto-grants-2004_11
ORD IDord-fb15be05056543b98ac3652867af0879
Quellennotizuspto-grants-2004_11