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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 452509Erstellt: 25. Oktober 2026

Bis(Chloromethyl) Ether → 7-[5-(3,5-Dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl]-1-methyl-3-(2-pyridylmethyl)-1,2,3,4-tetrahydroquinazoline-4-one

https://huagongshe.com/reaction/452509

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBis(Chloromethyl) EtherHCID 10967—
Edukt4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methylamino-N-(2-pyridylmethyl) benzoic acid amideHCID 66785191—
LösungsmittelDichloromethaneHCID 6344—
Produkt7-[5-(3,5-Dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl]-1-methyl-3-(2-pyridylmethyl)-1,2,3,4-tetrahydroquinazoline-4-oneHCID 2315982265,2%

Reaktionsschritte

In a solution of 0.06 g of 4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methylamino-N-(2-pyridylmethyl)benzoic acid amide (Compound of the present invention No. 5-332) synthesized similarly to Synthetic Example 18 in 5 ml of dichloromethane, 0.03 g of chloromethylether was added, and stirred at the same temperature for 15 hours. After the completion of the reaction, the solvent was distilled off under reduced pressure, and the residue was purified with silica gel column chromatography that was eluated with ethyl acetate-hexane (3:1) to obtain 0.04 g of the aimed product as colorless oily substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08492311B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-92fb4e793374411b95d987ebf38323b3
Quellennotizuspto-grants-2013_07