HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzylpiperazine-1-carboxamidine hemisulfate → HCID 178520340, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzylpiperazine-1-carboxamidine hemisulfate | HCID 2756652 | — |
| Reactant | HCID 66988753 | HCID 66988753 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178520340 | HCID 178520340 | 29% |
Reaction Steps
10.0 g (73.5 mmoles) of 2-hydroxymethylenebutyrolactone sodium salt [synthesized by the method described in J. O. Fissekis et al., J. Org., Chem. 29, 2670 (1964)] and 19.6 g (73.3 mmoles) of 1-amidino-4-benzylpiperazine sulfate were added to 360 ml of ethanol, and the solution was refluxed for 5 hours. Ethanol was evaporated, and the residue was mixed with water and extracted with chloroform. The chloroform layer was dried, concentrated, and purified by silica gel column chromatography to give 6.66 g (yield 29%) of 2-(4-benzylpiperazino)-4-hydroxy-5-(2-hydroxyethyl)pyrimidine as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04959368 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-dd64aadefc88404db465c46502ead374 |
| Source note | uspto-grants-1990_09 |