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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1156365Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/1156365

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
PatentnummerUS04335127
Quelldatensatzuspto-grants-1982_06
ORD IDord-45be1c0b95f7485189ed572b20128d75
Quellennotizuspto-grants-1982_06