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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238238Generated: October 30, 2026

Trifluoroacetic acid → 2-(1-piperidin-4-yl-ethyl)-3H-quinazolin-4-one

https://huagongshe.com/reaction/238238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-[1-(4-Oxo-3,4-dihydro-quinazolin-2-yl)-ethyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 136111511—
SolventDichloromethaneHCID 6344—
Product2-(1-piperidin-4-yl-ethyl)-3H-quinazolin-4-oneHCID 136111504—

Reaction Steps

A solution of 4-[1-(4-oxo-3,4-dihydro-quinazolin-2-yl)-ethyl]-piperidine-1-carboxylic acid tert-butyl ester and TFA in CH2Cl2 was stirred at r.t. for 6 hr. The precipitated solid was filtered and dried to afford the product as a white solid. (2 g, 90%). 1H NMR (DMSO-d6) δ 8.51 (br, s, 1H), 8.18 (br, s, 1H), 8.06 (d, 1H, J=7.6), 7.74 (t, 1H, J=8.0), 7.57 (d, 1H, J=8.0), 7.44 (t, 1H, J=8.0), 3.29-3.18 (m, 2H), 2.88-2.76 (m, 2H), 2.61-2.57 (m, 1H), 1.95-1.92 (m, 2H), 1.61-1.57 (m, 1H), 1.42-1.25 (m, 2H), 1.25 (d, 3H, J=6.8); ESI-MS m/z 258.1 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642609B2
Source datasetuspto-grants-2014_02
ORD IDord-2c0792c56e7c4ce9a8d3da1452c94d7b
Source noteuspto-grants-2014_02