HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-Dimethylamino-ethoxy)-benzoic acid → 5-{2-[2-(N,N-dimethylamino)ethyl]oxy-phenyl}-3-(4-hydroxy-phenyl)-1,2,4-oxadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-Dimethylamino-ethoxy)-benzoic acid | HCID 6484659 | — |
| Reactant | HCID 21863233 | HCID 21863233 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-{2-[2-(N,N-dimethylamino)ethyl]oxy-phenyl}-3-(4-hydroxy-phenyl)-1,2,4-oxadiazole | HCID 135704072 | — |
Reaction Steps
2,45 g of 2-[2-(N,N-dimethylamino)ethyl]oxy-benzoic acid are dissolved with 1.91 g of N-ethyl-N-dimethylaminopropyl)carbodiimide hydrochloride and catalytic amounts of hydroxybenzotriazole in 50 ml of DMF. After 15 minutes 1.52 g of 4-hydroxybenzoic acid amidoxime are added and the mixture is heated for 15 minutes at 700 W in the microwave. It is concentrated by evaporation, the residue is taken up in ethyl acetate, washed with water, dried over sodium sulphate and concentrated by evaporation in vacuo. The residue is filtered over silica gel with ethanol and converted into the salt as described above. Yield: 1.1 g (29% of theory). m.p.: 170° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06277872B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-395f7e2733714ed5a0676bfde1abe881 |
| Source note | uspto-grants-2001_08 |