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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156365Generated: October 26, 2026

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

https://huagongshe.com/reaction/1156365

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 numberUS04335127
Source datasetuspto-grants-1982_06
ORD IDord-45be1c0b95f7485189ed572b20128d75
Source noteuspto-grants-1982_06