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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472847Generated: October 30, 2026

2-(Benzenesulfonyl)-3-phenyloxaziridine → Methyl 2-(3,7-dichloro-2,5-dimethylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate

https://huagongshe.com/reaction/472847

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Benzenesulfonyl)-3-phenyloxaziridineHCID 320405—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantMethyl 2-(3,7-dichloro-2,5-dimethylpyrazolo[1,5-a]pyrimidin-6-yl)acetateHCID 86670281—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(3,7-dichloro-2,5-dimethylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetateHCID 8667028252.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of KHMDS (0.5 M in toluene, 1.04 mL) in THF (5 mL) at −78° C. was added a solution of methyl 2-(3,7-dichloro-2,5-dimethylpyrazolo[1,5-a]pyrimidin-6-yl)acetate (0.15 g, 0.5 mmol) in THF (5 mL) over 20 mins. The reaction mixture was stirred at −78° C. for 30 min. A solution of 3-phenyl-2-(phenylsulfonyl)-1,2-oxaziridine (0.16 g, 0.63 mmol) in THF (5 mL) was added over 10 min and the resulted reaction mixture was stirred for an additional 30 min at −78° C. The reaction mixture was quenched with saturated NH4Cl aqueous solution (2 mL). The mixture was allowed to warm up to room temperature and diluted with EtOAc (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, 30%). Used as is in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633200B2
Source datasetuspto-grants-2014_01
ORD IDord-e4ef436896d54597880e917cb8cc19c0
Source noteuspto-grants-2014_01