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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493715Generated: October 26, 2026

5,5-Dibromobarbituric acid → Tert-butyl 4-(2-bromo-3-oxopropyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/493715

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,5-Dibromobarbituric acidHCID 94877—
ReactantTert-butyl 4-(3-oxopropyl)piperidine-1-carboxylateHCID 10657745—
SolventDiethyl EtherHCID 3283—
ProductTert-butyl 4-(2-bromo-3-oxopropyl)piperidine-1-carboxylateHCID 23131015167%

Reaction Steps

To a solution of tert-butyl 4-(3-oxopropyl)piperidine-1-carboxylate (Wityak J., et al., J. Med. Chem., 40, p. 50 (1997): 27.6 g) in diethyl ether was added dibromobarbituric acid (17.0 g), and the mixture was mixed for 12 hours. The insolubles were filtered off, and the filtrate was diluted with diethyl ether, sequentially washed with a saturated aqueous sodium bicarbonate solution and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off to give the title compound (31.8 g) as a pale yellow viscous oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534887B2
Source datasetuspto-grants-2009_05
ORD IDord-5852e06dda4b4208955b6388ca012799
Source noteuspto-grants-2009_05