HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-Bromo-2-(4-(phenylsulfonyl)-1-piperazinyl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 5-Bromo-2-chloropyrimidine | HCID 606665 | — |
| Reactant | 1-(Benzenesulfonyl)piperazine hydrochloride | HCID 2756581 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-2-(4-(phenylsulfonyl)-1-piperazinyl)pyrimidine | HCID 39660614 | 50.5% |
Reaction Steps
A 250 mL round-bottomed flask was charged with 1-(phenylsulfonyl)piperazine hydrochloride (4.08 g, 15.51 mmol, Example 15, step 1), 5-bromo-2-chloropyrimidine (2.50 g, 12.92 mmol, Sigma-Aldrich, St. Louis, Mo.), and 20 mL of dioxane. To this was added triethylamine (4.50 mL, 32.3 mmol). After stirring at room temperature for 3 h, the mixture was diluted with water (50 mL) and the resulting precipitate was collected by filtration to give 5-bromo-2-(4-(phenylsulfonyl)-1-piperazinyl)pyrimidine (2.50 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431563B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-143ebc81d7de4196acfd56839e71b66e |
| Source note | uspto-grants-2013_04 |