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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850219Generated: October 30, 2026

Cyclobutanone → HCID 86730273, compound

https://huagongshe.com/reaction/1850219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutanoneHCID 14496—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86730270HCID 86730270—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86730273HCID 8673027362%

Reaction Steps

A solution of (S)-4-Isopropyl-3-[2-((S)-1-piperidin-4-yl-ethylamino)-pyrimidin-4-yl]-oxazolidin-2-one (28 mg, 0.084 mmol) in THF (2 mL) was added cyclobutanone (14 mg, 0.20 mmol) and sodium triacetoxyborohydride (28 mg, 0.13 mmol). The reaction was stirred at room temperature for 18 hours. The solvent is then removed under vacuum. The crude material was then purified using reverse phase C18 ODB column water-acetonitrile 0.1% TFA modifier to give (S)-3-{2-[(S)-1-(1-Cyclobutyl-piperidin-4-yl)-ethylamino]-pyrimidin-4-yl}-4-isopropyl-oxazolidin-2-one (20 mg) in 62% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957068B2
Source datasetuspto-grants-2015_02
ORD IDord-cbf01118e4f74cb1bb9173a64b554b0b
Source noteuspto-grants-2015_02