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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473594Generated: October 26, 2026

Piperazin-2-one → 1-Boc-3-(3-oxo-1-piperazinyl)azetidine

https://huagongshe.com/reaction/473594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazin-2-oneHCID 231360—
Reactant3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
Product1-Boc-3-(3-oxo-1-piperazinyl)azetidineHCID 5960543968.9%

Reaction Steps

To a mixture of 3-oxopiperazine 4a (490 mg, 4.89 mmol) and N-Boc-azetidin-3-one 1a (922 mg, 5.38 mmol) in 1,2-dichloroethane (10 mL) and HOAc (0.5 mL) was added Na(OAc)3BH (1141, 5.38 mmol). The reaction was stirred at room temperature overnight. Additional 1a (335 mg, 1.96 mmol) and Na(OAc)3BH (415 mg, 1.96 mmol) was added. The reaction was stirred for another 24 h before it was quenched with aq. NaHCO3. The resulting mixture was extracted with CH2Cl2. The organic solution was dried over Na2SO4 and concentrated. Purification by column chromatography (silica gel, 4% MeOH/CH2Cl2) gave intermediate 4b as white solid (860 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637498B2
Source datasetuspto-grants-2014_01
ORD IDord-6c6a32182fe444da9fcb8db27933f73c
Source noteuspto-grants-2014_01