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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355847Generated: October 30, 2026

2-(Benzenesulfonyl)-3-phenyloxaziridine → 5-Bromo-4-furan-2-yl-6-methanesulfinyl-pyrimidin-2-ylamine

https://huagongshe.com/reaction/1355847

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Benzenesulfonyl)-3-phenyloxaziridineHCID 320405—
Reactant5-Bromo-4-furan-2-yl-6-methylsulfanyl-pyrimidin-2-ylamineHCID 18507522—
SolventDichloromethaneHCID 6344—
Product5-Bromo-4-furan-2-yl-6-methanesulfinyl-pyrimidin-2-ylamineHCID 1850728661%

Reaction Steps

To a stirred suspension of 350 mg (1.22 mmol) 5-bromo-4-furan-2-yl-6-methylsulfanyl-pyrimidin-2-ylamine in 30 ml dichloromethane was added 1.28 g (4.89 mmol) 3-phenyl-2-(phenylsulfonyl)oxaziridine and stirring continued for 16 hours at room temperature. The reaction mixture was then concentrated in vacuo and the residue recrystallised from hexane/dichloromethane to afford 225 mg (61%) 5-bromo-4-furan-2-yl-6-methanesulfinyl-pyrimidin-2-ylamine as a beige crystalline solid. EI-MS m/e (%): 303 (M{flBr}+, 24), 301 (M{79Br}+24), 257(48), 255 (50), 198 (81), 196(84), 117(100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586441B2
Source datasetuspto-grants-2003_07
ORD IDord-cd06cf46cefa459c9cb93cc60644bb99
Source noteuspto-grants-2003_07