HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylhydrazine → HCID 44480787, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | HCID 58133724 | HCID 58133724 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 44480787 | HCID 44480787 | — |
Reaction Steps
Ethyl 6-(bromomethyl)-4-[4-cyano-2-(methylsulphonyl)phenyl]-2-oxo-1-[3-(trifluoromethyl)-phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylate (150 mg, 0.256 mmol; Example 19A) was initially charged in dioxane (3.5 ml). Phenylhydrazine (83.0 mg, 0.767 mmol) was added dropwise to the reaction mixture, and the mixture was then stirred at boiling point for 3 h. The reaction mixture was then separated directly by preparative HPLC (Method 12). This gave 9 mg (6% of theory) of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580800B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-1a3d2c296ad04a8986a28ecaf9fb914a |
| Source note | uspto-grants-2013_11 |