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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248251Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/1248251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantKetanserinHCID 3822—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
Product3-(2-(4-((4-Fluorophenyl)hydroxymethyl)-1-piperidinyl)ethyl)-2,4(1H,3H)-quinazolinedioneHCID 156394—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04522945
Source datasetuspto-grants-1985_06
ORD IDord-f947b5b120344dbda0d61256c471343e
Source noteuspto-grants-1985_06