HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272421Generated: October 28, 2026
2-(Benzenesulfonyl)-3-phenyloxaziridine → HCID 11188518, compound
https://huagongshe.com/reaction/272421
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Benzenesulfonyl)-3-phenyloxaziridine | HCID 320405 | — |
| Reactant | HCID 11199740 | HCID 11199740 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 11188518 | HCID 11188518 | 89% |
Reaction Steps
(8-Cyclopentyl-2-methylsulfanyl-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidin-6-yl)-carbamic acid tert-butyl ester (1.3 g, 3.45 mmol, prepared according to Example 8) was added to 50:50 dichloromethane/methanol (12 ml) followed by 2-benzenesulfonyl-3-phenyl-oxaziridine (1.08 g, 4.14 mmol). The mixture was stirred at 25° C. for 3.5 hours, evaporated to an oil and eluted through silica gel with chloroform. Fractions containing the product were evaporated to yield (8-cyclopentyl-2-methanesulfinyl-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidin-6-yl)-carbamic acid tert-butyl ester as a solid (1.2 g, 89%). MS (APCI); M++1: Calc'd, 393.15. Found 393.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456168B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-8cebc20c0bb84b0888727a4a044289fa |
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| Source note | uspto-grants-2008_11 |
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