Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351085Generated: October 25, 2026

N,N'-Dicyclohexylurea → 1,4-Dihydro-5-hydroxy-4-oxo-N-(tetrahydro-2-oxo-1(2H)-pyrimidinyl)-2-pyridinecarboxamide

https://huagongshe.com/reaction/2351085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DicyclohexylureaHCID 4277—
ReactantBistrimethylsilylacetamidHCID 11708267—
Reactant1,4-dihydro-4-oxo-5-(phenylmethoxy)-N-(tetrahydro-2-oxo-1(2H)-pyrimidinyl)-2-pyridine-carboxamideHCID 19848003—
SolventAcetonitrileHCID 6342—
Product1,4-Dihydro-5-hydroxy-4-oxo-N-(tetrahydro-2-oxo-1(2H)-pyrimidinyl)-2-pyridinecarboxamideHCID 19848013—

Reaction Steps

To a suspension of 1.71 g. (ca. 5 mmol) crude 1,4-dihydro-4-oxo-5-(phenylmethoxy)-N-(tetrahydro-2-oxo-1(2H)-pyrimidinyl)-2-pyridine-carboxamide in 22 ml acetonitrile was added 4.1 g (20 mmol) bis(trimethylsilyl)acetamide. After stirring for 20 minutes the undissolved dicyclohexylurea was filtered off and 0.85 g palladium on carbon were added to the filtrate. After the mixture had been hydrogenated for one hour, the catalyst was removed by filtration and 2.1 ml methanol and 0.1 ml acetic acid were added to the filtrate. After stirring overnight the desired product was filtered off and dried in vacuo. Yield 0.7 g, melting point 285°-290° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871841
Source datasetuspto-grants-1989_10
ORD IDord-7f931630bbd84374a778080aa84c9a6e
Source noteuspto-grants-1989_10