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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 345592Erstellt: 24. Oktober 2026

Potassium Iodide → cis-4-amino-5-chloro-N-[1-[2-(1,4-dihydro-2,4-dioxo-3(2H)-quinazolinyl)ethyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamide

https://huagongshe.com/de/reaction/345592

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
Edukt3-(2-chloroethyl)(1H,3H)quinazoline-2,4-dioneHCID 78766—
EduktSodium BicarbonateHCID 516892—
Edukt4-Amino-5-chloro-2-methoxy-N-[(3R,4S)-3-methoxypiperidin-4-YL]benzamideHCID 9861621—
LösungsmittelWaterHCID 962—
LösungsmittelMethyl Isobutyl KetoneHCID 7909—
Produktcis-4-amino-5-chloro-N-[1-[2-(1,4-dihydro-2,4-dioxo-3(2H)-quinazolinyl)ethyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamideHCID 15096932—

Reaktionsschritte

A mixture of 3.8 parts of 3-(2-chloroethyl)-2(1H), 4(3H)-quinazolinedione, 4.7 parts of cis-4-amino-5-chloro-2-methoxy-N-(3-methoxy-4-piperidinyl)benzamide, 1.7 parts of sodium hydrogen carbonate, 0.1 parts of potassium iodide and 160 parts of 4-methyl-2-pentanone was stirred and refluxed for 24 hours. Water was added to the reaction mixture. The precipitated product was filtered off and crystallized from N,N-dimethylformamide and a small amount of water, yielding 3.3 parts of cis-4-amino-5-chloro-N-[1-[2-(1,4-dihydro-2,4-dioxo-3(2H)-quinazolinyl)ethyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamide; mp. 270.8° C. (compound 142).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05057525
Quelldatensatzuspto-grants-1991_10
ORD IDord-8c48a1546add4af2891fc35251d6aaf5
Quellennotizuspto-grants-1991_10