Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161905Generated: October 29, 2026

Methyl iodide → N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-2-(1-methyl-2-piperidyl)-6-oxo-pyrimidine-4-carboxamide

https://huagongshe.com/reaction/1161905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTriethylamineHCID 8471—
Reactant4-FluorobenzylamineHCID 67326—
Reactant1-Carbobenzoxy-2-piperidinecarboxylic AcidHCID 4431026—
ReactantMethyl 5-(benzoyloxy)-1-methyl-6-oxo-2-piperidin-2-yl-1,6-dihydropyrimidine-4-carboxylateHCID 17961843—
SolventTetrahydrofuranHCID 8028—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductN-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-2-(1-methyl-2-piperidyl)-6-oxo-pyrimidine-4-carboxamideHCID 54677580—

Reaction Steps

Methyl 5-(benzoyloxy)-1-methyl-6-oxo-2-piperidin-2-yl-1,6-dihydropyrimidine-4-carboxylate (prepared from 1-(benzyloxycarbonyl)piperidine-2-carboxylic acid by procedures similar to those set forth in Examples 1 or 2 in combination with a deprotection step) was suspended in THF and treated with 3 eq. of triethylamine and 3 eq. of methyl iodide at 40° C. After stirring for 5 h, THF was evaporated and residue poured into EtOAc and washed with brine. Organic phase was dried (Na2SO4), filtered and concentrated under reduced pressure. The oily residue was taken into EtOAc and treated with 3 eq. of 4-fluorobenzylamine at 90° C. for 0.5 h. The title product was isolated as its trifluoroacetic salt by preparative RP-HPLC (C18, 5 μM, acetonitrile/water containing 0.1% TFA as eluant).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820660B2
Source datasetuspto-grants-2010_10
ORD IDord-1ed7869ede5245a09cbeaaeffe35d52b
Source noteuspto-grants-2010_10