HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylbarbituric acid → HCID 23131006, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylbarbituric acid | HCID 69860 | — |
| Reactant | HCID 140536539 | HCID 140536539 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23131006 | HCID 23131006 | 62.7% |
Reaction Steps
To a solution of allyl (2Z)-5-(1-(3-((6-chloro-2-naphthyl)sulfonyl)propanoyl)-4-piperidinyl)-3-methyl-1,3-thiazol-2(3H)-ylidenecarbamate (0.60 g) obtained in Example 57d) in THF, 1,3-dimethylbarbituric acid (0.25 g) and tetrakis(triphenylphosphine)palladium (0.06 g) were added thereto and mixed for 12 hours under argon atmosphere. The insolubles were filtered off, and the filtrate was concentrated. The residue was purified with a silica gel column to give the title compound (0.32 g) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534887B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-39bd1d007bf54cc289b182fa7f980bb8 |
| Source note | uspto-grants-2009_05 |