HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 86758373, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 5-Nitro-2-Furoic Acid | HCID 12577 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | Ternidazole | HCID 68944 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86758373 | HCID 86758373 | — |
Reaction Steps
The reaction mixture of 5-nitro-2-furoic acid (157 mg, 1.0 mmol), 1-(3-hydroxypropyl)-2-methyl-5-nitroimidazole (184 mg, 1.0 mmol), EDCI (260 mg, 1.3 mmol), DMAP (10 mg, 0.1 mmol) and THF (5 ml) will be stirred at room temperature for 10 h. Evaporation of THF gives a residue which will be dissolved in ethyl acetate. The organic layer of ethyl acetate will be washed with H2O, 5% Na2CO3, H2O and brine, and then dried over MgSO4. The solvent will be removed under vacuum. The resulting solid will be recrystallized from C2H5OH to give 2-methyl-5-nitro-1H-imidazole-1-propyl 5-nitro-2-furoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06423707B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-6818a41e648c4729852d93a1dba42897 |
| Source note | uspto-grants-2002_07 |