HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 2-(4-Amino-1,3-dimethyl-5-pyrazolyl)-4,5-dimethylimidazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,3-Butanediamine | HCID 136362 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 4-Amino-1,3-dimethyl-1H-pyrazole-5-carbonitrile | HCID 12335816 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(4-Amino-1,3-dimethyl-5-pyrazolyl)-4,5-dimethylimidazoline | HCID 14006583 | 91.7% |
Reaction Steps
A mixture of 7 g (0.05 mol) of 4-amino-5-cyano-1,3-dimethylpyrazole, 5 g (0.057 mol) of 2,3-diaminobutane and 10.5 g (0.055 mol) of p-toluene sulfonic acid hydrate is heated in an oil bath at 180°-200° C. for seven hours. The yellow melt is dissolved in 200 ml of chloroform and stirred with 100 ml of 20% aqueous sodium carbonate solution. The organic layer is separated, dried over MgSO4 and evaporated in vacuo to give 9.5 g of 2-(4-amino-1,3-dimethyl-5-pyrazolyl)-4,5-dimethylimidazoline and characterized as a dihydrochloride salt, mp 250° C. from 20% isopropanolic HCl and ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04469868 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-a6e93a42d1764eadad75bcf770abc096 |
| Source note | uspto-grants-1984_09 |