HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 54169144, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 54185645 | HCID 54185645 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 54169144 | HCID 54169144 | — |
Reaction Steps
2.7 gm (0.01 mol) of 4-chloro-5-cyano-6-methyl-2-(1-oxido-thiomorpholino)-pyrimidine (m.p. 251°-253°C, obtained from 5-cyano-2,4-dichloro-6-methyl-pyrimidine and thiomorpholine-1-oxide in acetone while cooling) were refluxed with a solution of 8.6 gm (0.1 mol) of piperazine in 80 ml of dioxane for about 30 minutes. The major part of the solvent was distilled off in vacuo, the residue was dissolved in about 80 ml of water, and a small quantity of 8 N sodium hydroxide was added, whereby the reaction product was first obtained as greasy, but soon solidifying precipitate. The product was suction-filtered off, washed with water and dried. Yield: 2.8 gm (87% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03975384 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-627a58757b8b43599090229d6b394937 |
| Source note | uspto-grants-1976_08 |