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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1248251Erstellt: 27. Oktober 2026

Methanol → 3-(2-(4-((4-Fluorophenyl)hydroxymethyl)-1-piperidinyl)ethyl)-2,4(1H,3H)-quinazolinedione

https://huagongshe.com/reaction/1248251

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktKetanserinHCID 3822—
EduktSodium borohydrideHCID 4311764—
LösungsmittelWaterHCID 962—
Produkt3-(2-(4-((4-Fluorophenyl)hydroxymethyl)-1-piperidinyl)ethyl)-2,4(1H,3H)-quinazolinedioneHCID 156394—

Reaktionsschritte

To a stirred mixture of 2.6 parts of 3-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]-2,4(1H,3H)-quinazolinedione and 120 parts of methanol are added portionwise 2 parts of sodium borohydride. Upon completion, stirring is continued overnight at room temperature. Water is added and the whole is evaporated. The residue is stirred in water. The solid product is filtered off and crystallized from 2-propanone, yielding 1.2 parts of 3-[2-[4-[(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]ethyl]-2,4(1H,3H)-quinazolinedione; mp. 212.8° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04522945
Quelldatensatzuspto-grants-1985_06
ORD IDord-f947b5b120344dbda0d61256c471343e
Quellennotizuspto-grants-1985_06