HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Benzenesulfonyl)-3-phenyloxaziridine → 5-Bromo-4-furan-2-yl-6-methanesulfinyl-pyrimidin-2-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Benzenesulfonyl)-3-phenyloxaziridine | HCID 320405 | — |
| Reactant | 5-Bromo-4-furan-2-yl-6-methylsulfanyl-pyrimidin-2-ylamine | HCID 18507522 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-4-furan-2-yl-6-methanesulfinyl-pyrimidin-2-ylamine | HCID 18507286 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06586441B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-cd06cf46cefa459c9cb93cc60644bb99 |
| Source note | uspto-grants-2003_07 |