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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Benzenesulfonyl)-3-phenyloxaziridine | HCID 320405 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | HCID 86695063 | HCID 86695063 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86695064 | HCID 86695064 | 22% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034882B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-29e90067c5b44e8682ba38da3363d5d8 |
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| Source note | uspto-grants-2015_05 |
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