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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574328Generated: October 31, 2026

2-(Benzenesulfonyl)-3-phenyloxaziridine → HCID 86695064, compound

https://huagongshe.com/reaction/574328

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Benzenesulfonyl)-3-phenyloxaziridineHCID 320405—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 86695063HCID 86695063—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86695064HCID 8669506422%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of KHMDS (0.5 M in toluene, 1.50 mL, 0.78 mmol) in THF (12 mL) at −78° C. was added a solution of methyl 2-(2-(3-(benzyloxy)phenyl)-7-chloro-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)acetate (0.35 g, 0.83 mmol) in THF (12 mL) dropwise over 40 min. The mixture was stirred at −78° C. for 30 min. A solution of 3-phenyl-2-(phenylsulfonyl)-1,2-oxaziridine (0.33 g, 1.25 mmol) in THF (24 mL) was added over 20 min and the reaction mixture was stirred for additional 30 min at −78° C. The reaction mixture was quenched with saturated NH4Cl aqueous solution (2 mL). The reaction mixture was allowed to warm to room temperature and then diluted with ethyl acetate (100 mL). The organic phase was washed with water and brine and dried with sodium sulfate. The solvent was evaporated. Purification by silica gel chromatography provided the title compound (80 mg, 22%). Used as is in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034882B2
Source datasetuspto-grants-2015_05
ORD IDord-29e90067c5b44e8682ba38da3363d5d8
Source noteuspto-grants-2015_05