HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzoxazolinone, 5-bromo- → (S)-N-[methyl(oxo)phenyl-lambda6-sulfanylidene]-5-[(2-oxo-2,3-dihydro-1,3-benzoxazol-5-yl)ethynyl]nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzoxazolinone, 5-bromo- | HCID 26853 | — |
| Reactant | (S)-N-[methyl(oxo)phenyl-lambda6-sulfanylidene]-5-[(trimethylsilyl)ethynyl]nicotinamide | HCID 24953135 | — |
| Product | (S)-N-[methyl(oxo)phenyl-lambda6-sulfanylidene]-5-[(2-oxo-2,3-dihydro-1,3-benzoxazol-5-yl)ethynyl]nicotinamide | HCID 24954922 | 40.5% |
Reaction Steps
In a manner similar to that described in Example 443, (S)—N-[methyl(oxo)phenyl-λ6-sulfanylidene]-5-[(trimethylsilyl)ethynyl]nicotinamide (150 mg, 0.42 mmol) and 5-bromo-2-benzoxazolinone (102 mg, 0.46 mmol) were reacted to give the title compound as light yellow solid (71 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383825B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-8ad6709809d0419eb1a9f7a0ce0acbca |
| Source note | uspto-grants-2013_02 |