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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127273Erstellt: 26. Oktober 2026

Sodium Carbonate → 1-[1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-piperidinyl]-4,4-dimethyl-piperidin-2,6-dione monohydrochloride

https://huagongshe.com/reaction/127273

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt2-Chloro-6,7-dimethoxy-4-quinazolinamineHCID 90235—
Edukt4,4-Dimethyl[1,4'-bipiperidine]-2,6-dioneHCID 12822562—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-[1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-piperidinyl]-4,4-dimethyl-piperidin-2,6-dione monohydrochlorideHCID 20556260—

Reaktionsschritte

The mixture of 4.79 g of 4-amino-2-chloro-6,7-dimethoxyquinazoline, 4.49 g of 4,4-dimethyl-1-(4-piperidinyl)-piperidin-2,6-dione, 4.24 g of anhydrous sodium carbonate and 75 ml of dimethylformamide is stirred at 150° under nitrogen for 6 hours. It is filtered, the filtrate evaporated, the residue dissolved in ethyl acetate and the solution washed with aqueous sodium carbonate and water. It is dried, evaporated, the residue triturated with isopropanol, filtered off and discarded. The filtrate is made strongly acidic with hydrogen chloride, the precipitate filtered off and triturated with 175 ml of boiling methanol, to yield the 1-[1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-piperidinyl]-4,4-dimethyl-piperidin-2,6-dione monohydrochloride, melting at 279°-280° with decomposition.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04255429
Quelldatensatzuspto-grants-1981_03
ORD IDord-a4e04b06a28b4d3a9bdb79429e524ff1
Quellennotizuspto-grants-1981_03