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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097283Generated: October 31, 2026

5-Amino-5-ethyl-1-phenylbarbituric acid → N-(5-Ethyl-hexahydro-2,4,6-trioxo-1-phenyl-5-pyrimidinyl)-2,3,4,5-tetrafluorobenzamide

https://huagongshe.com/reaction/1097283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-5-ethyl-1-phenylbarbituric acidHCID 15424937—
ReactantN-(1-Ethyl-hexahydro-5-methyl-2,4,6-trioxo-5-pyrimidinyl)-2,3,4,5-tetrafluorobenzamideHCID 24765666—
ProductN-(5-Ethyl-hexahydro-2,4,6-trioxo-1-phenyl-5-pyrimidinyl)-2,3,4,5-tetrafluorobenzamideHCID 24765564—

Reaction Steps

Compound 20k was prepared by the same method described for 20f using 5-amino-5-ethyl-1-phenylbarbituric acid (0.50 g, 2 mmol). The crude 5-ethyl-1-phenyl-5-(tetrafluorobenz-amido)barbituric acid (20k) was obtained as yellow crystals that were pure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143252B2
Source datasetuspto-grants-2012_03
ORD IDord-31fcb5f2b20d40d192ce55cbffc9c114
Source noteuspto-grants-2012_03