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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1250565Erstellt: 26. Oktober 2026

Piperidine → 2-Chloro-6-nitro-4-piperidinoquinazoline

https://huagongshe.com/reaction/1250565

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidineHCID 8082—
EduktPhosphorus oxychlorideHCID 24813—
Edukt6-Nitro-2,4(1H,3H)-quinazolinedioneHCID 816982—
LösungsmittelWaterHCID 962—
Produkt2-Chloro-6-nitro-4-piperidinoquinazolineHCID 18326509—

Reaktionsschritte

To 367 mg (1.77 mmol) of 6-nitroquinazoline-2,4 (1H,3H)-dione was added 15.13 g (98.70 mmol) of phosphorus oxychloride to effect reaction in the same manner as in Example 10. Next, to the reaction mixture was added dropwise 301 mg (3.54 mmol) of piperidine under ice cooling, and the resulting mixture was stirred under ice cooling for 2 hours. Water was added to the reaction mixture, and crystals thus precipitated were filtered out to obtain 2-chloro-6-nitro-4-piperidinoquinazoline. The compound was dissolved in 1 ml of DMF, and after 1.52 g (26.65 mmol) of allylamine was added to the resulting solution, the resulting mixture was stirred at room temperature for 2.5 hours. Water was added to the reaction mixture, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by a silica gel column to give 213 mg (yield: 38.4%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06339089B2
Quelldatensatzuspto-grants-2002_01
ORD IDord-8d9ae0c038e542ffa98a4345f542b98d
Quellennotizuspto-grants-2002_01