HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Oxazolidinone, 5,5-dimethyl- → 3-{5-[4-(5-Cyano-3-methylpyridin-2-yl)piperazine-1-carbonyl]pyridin-2-yl}-5,5-dimethyloxazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Oxazolidinone, 5,5-dimethyl- | HCID 136892 | — |
| Reactant | 6-[4-(6-Bromopyridine-3-carbonyl)piperazin-1-yl]-5-methylnicotinonitrile | HCID 58484518 | — |
| Product | 3-{5-[4-(5-Cyano-3-methylpyridin-2-yl)piperazine-1-carbonyl]pyridin-2-yl}-5,5-dimethyloxazolidin-2-one | HCID 58484711 | 51.6% |
Reaction Steps
By reaction and treatment in the same manner as in Example 1 and using 6-[4-(6-bromopyridine-3-carbonyl)piperazin-1-yl]-5-methylnicotinonitrile (105 mg) described in Preparation Example 131 and 5,5-dimethyloxazolidin-2-one (47 mg) described in Preparation Example 43, the title compound (59 mg) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354401B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-e45cff29b771472c9ef460a0d7cdcf77 |
| Source note | uspto-grants-2013_01 |