HuagongsheHuagongshe Chemistry Print Report · For research reference only
5,5-Dibromobarbituric acid → Tert-butyl 4-(2-bromo-3-oxopropyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5,5-Dibromobarbituric acid | HCID 94877 | — |
| Reactant | Tert-butyl 4-(3-oxopropyl)piperidine-1-carboxylate | HCID 10657745 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Tert-butyl 4-(2-bromo-3-oxopropyl)piperidine-1-carboxylate | HCID 23131015 | 167% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534887B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-5852e06dda4b4208955b6388ca012799 |
| Source note | uspto-grants-2009_05 |