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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49151Generated: October 26, 2026

Propionamide → N-(4-{4-[5-(2-ethoxy-ethyl)-2,4,6-trioxo-hexahydro-pyrimidin-5-yloxy]-phenoxy}-benzyl)-propionamide

https://huagongshe.com/reaction/49151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionamideHCID 6578—
Reactant5-DeceneHCID 23916—
Reactant4,4',5,5,5',5'-Hexafluoro-2,2,2',2'-tetrakis(trifluoromethyl)-4,4'-bi-1,3-dioxolaneHCID 197408—
ReactantN-[4-(4-Hydroxy-phenoxy)-benzyl]-propionamideHCID 20636237—
Reactant5-Bromo-5-(2-ethoxy-ethyl)-pyrimidine-2,4,6-trioneHCID 21931123—
SolventAcetonitrileHCID 6342—
ProductN-(4-{4-[5-(2-ethoxy-ethyl)-2,4,6-trioxo-hexahydro-pyrimidin-5-yloxy]-phenoxy}-benzyl)-propionamideHCID 20636226—

Reaction Steps

Following the procedure outlined for the preparation of Example 1, N-[4-(4-hydroxy-phenoxy)-benzyl]-propionamide (0.13 g, 0.47 mmol) was reacted with 5-bromo-5-(2-ethoxy-ethyl)-pyrimidine-2,4,6-trione (0.13 g, 0.48 mmol), 1,5,7-trazabicyclo[4.4.0]dec-5-ene bound to polystyrene crosslinked with 2% DVB (PTBD, Fluka, 0.31 g) and 1.55 mL of acetonitrile, benzyl)-propionamide (0.060 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706723B2
Source datasetuspto-grants-2004_03
ORD IDord-4a89fc67434542439b5e46a12ded1604
Source noteuspto-grants-2004_03