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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Benzenesulfonyl)-3-phenyloxaziridine | HCID 320405 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | Methyl 2-(3,7-dichloro-2,5-dimethylpyrazolo[1,5-a]pyrimidin-6-yl)acetate | HCID 86670281 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(3,7-dichloro-2,5-dimethylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate | HCID 86670282 | 52.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633200B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-e4ef436896d54597880e917cb8cc19c0 |
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| Source note | uspto-grants-2014_01 |
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