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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44627Erstellt: 24. Oktober 2026

Iodine → HCID 57444149, Verbindung

https://huagongshe.com/de/reaction/44627

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktIsoamyl NitriteHCID 8053—
EduktCesium iodideHCID 24601—
Edukt8-amino-1-methyl-N-[(1S)-2-morpholin-4-yl-1-phenylethyl]-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamideHCID 57444150—
KatalysatorCopper iodideHCID 83717—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
ProduktHCID 57444149HCID 5744414940%

Reaktionsschritte

To a well stirred and warm suspension of 8-amino-1-methyl-N-[(1S)-2-morpholin-4-yl-1-phenylethyl]-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide (3 g, 6.92 mmol) in dimethoxyethane (240 mL), maintained in an inert atmosphere of argon, cesium iodide (2.16 g, 8.3 mmol), bisublimated iodine (870 mg, 3.46 mmol), copper iodide (460 mg, 2.42 mmol) and isopentyl nitrite (1.71 mL, 1.5 g, 12.46 mmol) were added, in sequence. The reaction mixture was stirred vigorously at 65-70° C. for 18 hours. After cooling in an ice-water bath, the solid was filtered off and the filtrate was diluted with dichloromethane (100 mL), washed with 30% ammonium hydroxide (50 mL), sodium thiosulphate (100 mL), brine and dried over anhydrous Na2SO4. The crude was purified by flash chromatography on silica gel (eluant: dichloromethane/methanol 95:59) and 1.48 g of the title compound was isolated (40% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541429B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-b27aceb55e484bbc8f9a5441de48ba65
Quellennotizuspto-grants-2013_09