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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Benzenesulfonyl)-3-phenyloxaziridineHCID 320405—
ReactantHCID 11199740HCID 11199740—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 11188518HCID 1118851889%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456168B2
Source datasetuspto-grants-2008_11
ORD IDord-8cebc20c0bb84b0888727a4a044289fa
Source noteuspto-grants-2008_11