HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186172Generated: October 30, 2026
Tert-butyl 3-oxopiperazine-1-carboxylate → HCID 86586605, compound
https://huagongshe.com/reaction/2186172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-butyl 3-oxopiperazine-1-carboxylate | HCID 3157178 | — |
| Reactant | HCID 23447336 | HCID 23447336 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 86586605 | HCID 86586605 | 76.6% |
Reaction Steps
To a solution of 6-(6-chloropyrimidine-4-yl)-1-oxa-6-azaspiro[2,5]octane (4.00 g) and 4-(tert-butoxycarbonyl)-2-piperazinone (3.38 g) in tert-butylalcohol (50 ml) was added potassium tert-butoxide (0.57 g), and the mixture was stirred at 80° C. overnight. The reaction solution was concentrated, and the residue was diluted with ethyl acetate (100 ml), washed with 0.5N hydrochloric acid and saturated brine, dried and concentrated. The residue was purified with silica gel column chromatography (eluent:ethyl acetate) and crystallized from a mixture of ethyl acetate and diethylether to give colorless crystals of 4-(tert-butoxycarbonyl)-1-[1-(6-chloro-4-pyrimidinyl)-4-hydroxypiperidin-4-ylmethyl]piperazin-2-one (5.51 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403595B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-55bf84e558d14ffaa1274f57778cc3df |
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| Source note | uspto-grants-2002_06 |
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