Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67080Generated: October 30, 2026

Sodium borohydride → 2(1H)-Quinazolinone, 3,4-dihydro-3-(1-(2-(4-chlorophenyl)-2-hydroxyethyl)-4-piperidinyl)-

https://huagongshe.com/reaction/67080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-Chlorobenzoylmethyl)-4-[3,4-dihydro-2(1H)-quinazolinon-3-yl]-piperidineHCID 12797993—
SolventMethanolHCID 887—
Product2(1H)-Quinazolinone, 3,4-dihydro-3-(1-(2-(4-chlorophenyl)-2-hydroxyethyl)-4-piperidinyl)-HCID 306138758.6%

Reaction Steps

In this example, 2.70 g of 1-(4-chlorobenzoylmethyl)-4-[3,4-dihydro-2(1H)-quinazolinon-3-yl]-piperidine and 150 ml of methanol are mixed and stirred at room temperature. To the stirred mixture, 2.0 g of sodium borohydride is added over a period of 5 hours. Then, the resultant mixture is stirred overnight at room temperature. The white crystals deposited are separated by filtration, successively washed with methanol and water and dried to obtain 2.07 g of a crude product. The crude product is recrystallized from a mixed solvent of chloroform and ethanol to obtain 1.59 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04344948
Source datasetuspto-grants-1982_08
ORD IDord-992b58a31d184306a098a05d791f8bd3
Source noteuspto-grants-1982_08