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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097282Generated: October 31, 2026

5-Amino-1-cyclohexyl-5-ethylbarbituric acid → N-(1-Cyclohexyl-5-ethyl-hexahydro-2,4,6-trioxo-5-pyrimidinyl)-2,3,4,5-tetrafluorobenzamide

https://huagongshe.com/reaction/1097282

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-1-cyclohexyl-5-ethylbarbituric acidHCID 15424936—
ReactantN-(1-Ethyl-hexahydro-5-methyl-2,4,6-trioxo-5-pyrimidinyl)-2,3,4,5-tetrafluorobenzamideHCID 24765666—
ProductN-(1-Cyclohexyl-5-ethyl-hexahydro-2,4,6-trioxo-5-pyrimidinyl)-2,3,4,5-tetrafluorobenzamideHCID 24765664—

Reaction Steps

Compound 20i was prepared by the same method described for 20f using 5-amino-1-cyclohexyl-5-ethylbarbituric acid (0.51 g, 2 mmol). The crude 1-cyclohexyl-5-ethyl-5-(tetrafluorobenzamido)barbituric acid (20i) was obtained as yellow crystals and did not require further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143252B2
Source datasetuspto-grants-2012_03
ORD IDord-6cc2f9e571234ef994b129593e09ffb4
Source noteuspto-grants-2012_03