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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23530Generated: October 30, 2026

Trifluoroacetic acid → Tert-butyl 4-[2-oxo-2-(4-pyridinyl)ethyl]-2-pyridinylcarbamate

https://huagongshe.com/reaction/23530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178452644HCID 178452644—
SolventDichloromethaneHCID 6344—
ProductAmmonium HydroxideHCID 14923—
ProductTert-butyl 4-[2-oxo-2-(4-pyridinyl)ethyl]-2-pyridinylcarbamateHCID 2257413250%

Reaction Steps

Trifluoroacetic acid (8 mL) was added to tert-butyl 4-[2-phenyl-4-(4-pyridinyl)-1H-imidazol-5-yl]-2-pyridinylcarbamate in dichloromethane (10 mL) and after 42 h, the volatiles were removed under reduced pressure. The residue was diluted with ethyl acetate and was washed with st. K2CO3, dried over Na2SO4, filtered and concentrated in vacuo to give a yellow solid which was purified by silica gel chromatography, eluting with 95 CH2Cl2:5 CH3OH:0.5 NH4OH to afford the 258 mg (50%) of the titled compound as a yellow solid. Step D: 4-(2-phenyl-4-pyridin-4-yl-1H-imidazol-5-yl)pyridin-2(1H)-one

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852727B2
Source datasetuspto-grants-2005_02
ORD IDord-4a48228f49e0452baa2414d569a2f24c
Source noteuspto-grants-2005_02