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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217268Generated: November 3, 2026

3,4-dihydro-6-[2-(dimethylamino)ethoxy]-3-(1-phenylmethyl-4-piperidinyl)-2(1H)-quinazolinone → 3,4-dihydro-6-[2-(dimethylamino)ethoxy]-3-(4-piperidinyl)-2(1H)-quinazolinone

https://huagongshe.com/reaction/2217268

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-6-[2-(dimethylamino)ethoxy]-3-(1-phenylmethyl-4-piperidinyl)-2(1H)-quinazolinoneHCID 17958700—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product3,4-dihydro-6-[2-(dimethylamino)ethoxy]-3-(4-piperidinyl)-2(1H)-quinazolinoneHCID 17958686—

Reaction Steps

A mixture of 0.9 g (0.0022 mol) of 3,4-dihydro-6-[2-(dimethylamino)ethoxy]-3-(1-phenylmethyl-4-piperidinyl)-2(1H)-quinazolinone, 10 mL methanol, and 0.5 g palladium(II) hydroxide (Pearlman's catalyst) was hydrogenated until the uptake of hydrogen ended. The catalyst was filtered off, the filtrate was evaporated down in vacuo, and the residue remaining was used in the next step without any further purification. Yield: 0.6 g (86% of theoretical). IR (KBr): 1662 (C═O) cm−1; MS: M+=318.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407963B2
Source datasetuspto-grants-2008_08
ORD IDord-072a7b45ccac44d5bd79958f6e0242ff
Source noteuspto-grants-2008_08