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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1169280Erstellt: 26. Oktober 2026

Mecloqualone → 3-(2-Chloro-phenyl)-2-(2-dimethylamino-vinyl)-3,4-dihydro-quinazolin-4-one

https://huagongshe.com/reaction/1169280

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMecloqualoneHCID 9567—
EduktDimethylformamide dimethyl acetalHCID 78373—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(2-Chloro-phenyl)-2-(2-dimethylamino-vinyl)-3,4-dihydro-quinazolin-4-oneHCID 5368976962,4%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

A mixture of 3-(2-chloro-phenyl)-2-methyl-3,4-dihydro-quinazolin-4-one (1.0 g, 3.69 mmol) and dimethylformamide dimethyl acetal (0.64 mL, 4.8 mmol) in dimethylformamide (4 mL) was heated to 140° C. for 24 hours. Additional dimethylformamide dimethyl acetal (0.32 mL, 2.4 mmol) was added and heating was continued for an additional 24 hours. The reaction was cooled to ambient temperature and concentrated at reduced pressure (60° C. bath temperature). The dark residue was triturated with methanol and the pale orange solid which formed was collected and dried to give 0.75 g (62%) of 3-(2-chloro-phenyl)-2-(2-dimethylamino-vinyl)-3,4-dihydro-quinazolin-4-one which had: mp 228-230° C.; 1H 1H NMR δ 8.19 (d, J=8 Hz, 1H), 7.91 (d, J=12.3 Hz, 1H), 7.71-7.18 (m, 7H), 4.10 (d, J=12.3 Hz, 1H), 2.81 (br s, 6H). Analysis calculated for C18H16ClN3O: C, 66.36; H, 4.95; N, 12.90. Found: C, 66.20; H, 5.03; N, 12.79.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06627755B1
Quelldatensatzuspto-grants-2003_09
ORD IDord-a82b0769025d42b38648c587b336da1e
Quellennotizuspto-grants-2003_09