HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propylamine → 5-Amino-2-benzyl-1-n-propylimidazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | 2-Amino-2-cyanoacetamide | HCID 98341 | — |
| Reactant | Ethyl 2-phenylacetimidate hydrochloride | HCID 12218775 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Amino-2-benzyl-1-n-propylimidazole-4-carboxamide | HCID 69964203 | 21.1% |
Reaction Steps
A solution of 2-amino-2-cyanoacetamide (prepared as described in WO 94/00453; 250 mg, 2.5 mmol) in acetonitrile (6 mL) was added to ethyl 2-phenylethanimidoate hydrochloride (prepared as described in J. Med. Chem. 38 (18), 3676 (1995); 500 mg, 2.5 mmol), and the suspension stirred at room temperature for an hour, then cooled in an ice-bath. The resulting precipitate was filtered off, n-propylamine (160 μL, 2.5 mmol) added to the filtrate and the solution stirred at room temperature for 72 hours. The reaction mixture was concentrated under reduced pressure, and the residue purified by column chromatography on silica gel using dichloromethane:methanol (95:5) as eluant to afford the title compound as a tan coloured solid (136 mg, 21%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06586439B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-ccc03095f61e473ca81f31aacc9f420a |
| Source note | uspto-grants-2003_07 |