HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 19763654, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 67821553 | HCID 67821553 | — |
| Product | HCID 19763654 | HCID 19763654 | 81% |
Reaction Steps
To a solution of 4'-[[5,7-dimethyl-2-ethyl-3H-imidazo[4,5-b]pyridin-3-yl]methyl][1,1'-biphenyl-2-yl]carboxylic acid hydrazide (400 mg, 1 mmol) and triethylamine (130 mg, 1.3 mmol) in THF (20 mL) was added carbonyldiimidazole (275 mg, 1.7 mmcl) at 0° C. The reaction mixture was stirred at room temperature overnight and the solvent was evaporated. The residue was dissolved in water and the solution was adjusted to pH 3 by the addition of IN HCl. The resulting precipitate was collected by filtration and dried under vacuum to give 5- [4'-[[5,7-dimethyl-2-ethyl-3H-imidazo[4,5-b]pyridin 3-yl]methyl][1,1'-biphenyl-2-yl]-1,3,4 oxadiazol-2[3H]-one (0.35 g, 81%) as a partial hydrate, mp 210°-212° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05210204 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-4332bb37fdda494fa3194a58c743c22d |
| Source note | uspto-grants-1993_05 |