HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-[3-(1H-indazol-5-yl)-1,2,4-oxadiazol-5-yl]-2-[(1-methylethyl)oxy]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Cyano-4-isopropoxybenzoyl chloride | HCID 57505842 | — |
| Reactant | HCID 178513242 | HCID 178513242 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-[3-(1H-indazol-5-yl)-1,2,4-oxadiazol-5-yl]-2-[(1-methylethyl)oxy]benzonitrile | HCID 53247367 | 20.2% |
Reaction Steps
3-Cyano-4-[(1-methylethyl)oxy]benzoyl chloride (D106) (545 mg, 2.437 mmol) and N-hydroxy-1H-indazole-5-carboximidamide (D2) (685 mg, 2.437 mmol) were dissolved in acetonitrile (30 ml) before adding triethylamine (0.374 ml, 2.68 mmol). The resulting mixture was stirred at room temperature for 3 h then at 80° C. for 48 h, then cooled at room temperature. The precipitate formed was filtered off and dissolved in EtOAc and washed with water, evaporated and chromatographed [0-15% EtOAc in cyclohexane] to give the title compound (170 mg, 17%) as a pink solid. MS (ES): C19H15N5O2 requires 345; found (MH+) 346
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324254B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-c7f25a267cde4006be43d6e2ca68044e |
| Source note | uspto-grants-2012_12 |