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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2187601Erstellt: 24. Oktober 2026

Methane → Jtc-801

https://huagongshe.com/de/reaction/2187601

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
EduktEthanolHCID 702—
EduktOxalyl chlorideHCID 65578—
Edukt2-Methylquinoline-4,6-diamineHCID 223995—
EduktSodium BicarbonateHCID 516892—
LösungsmittelPyridineHCID 1049—
ProduktJtc-801HCID 531133959%

Reaktionsschritte

To a solution of 2-[(4-ethylphenoxy)methyl]benzoic acid (1.13 g, 4.4 mmol) obtained in Preparation Example 2-1 in chloroform (20 ml) was added oxalyl chloride (0.6 ml, 6.8 mmol) and the mixture was stirred at room temperature for 1 hr. Then the reaction mixture was concentrated under reduced pressure. To the obtained acid chloride were added pyridine (20 ml) and 4,6-diamino-2-methylquinoline (623 mg, 4 mmol) obtained in Preparation Example 1-1 and the mixture was stirred at room temperature for 10 hr. To the reaction mixture was added an aqueous sodium hydrogencarbonate solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over sodium sulfate, and the solvent was evaporated. The obtained crude product was dissolved in ethanol and treated with active charcoal, and the solvent was evaporated. The obtained residue was dissolved in ethyl acetate and 1N hydrochloric acid-ether solution was added. The resulting precipitate was collected by filtration. The obtained solid was heated and dried under reduced pressure to give the title compound (1.06 g, 59%, pale-yellow crystals).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06410561B1
Quelldatensatzuspto-grants-2002_06
ORD IDord-877dd52c90344404af587b56784ff73d
Quellennotizuspto-grants-2002_06