HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Azetidinone → HCID 24739471, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Azetidinone | HCID 136721 | — |
| Reactant | HCID 24738994 | HCID 24738994 | — |
| Product | HCID 24739471 | HCID 24739471 | 6% |
Reaction Steps
As described for Example 60, 6-iodo-2-(5-methyl-3-phenyl-isoxazol-4-yl)-imidazo[1,2-a]pyridine (100 mg, 0.25 mmol) was converted, using 2-azetidinone instead of benzamide, to the title compound (4.8 mg, 6%) which was obtained as a light yellow oil. MS: m/e=345.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585874B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-a8442310d5024fd28b60da03bf85e13a |
| Source note | uspto-grants-2009_09 |