HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 4-Methoxy-2-(3-methyl-1,2,4-oxadiazol-5-yl)benzenamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-Hydroxyacetamidine | HCID 30926 | — |
| Reactant | Methyl 2-amino-5-methoxybenzoate | HCID 13052275 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methoxy-2-(3-methyl-1,2,4-oxadiazol-5-yl)benzenamine | HCID 19962123 | 72.4% |
Reaction Steps
Sodium hydride (594 mg) was added to a stirred suspension of acetamide oxime (1.0 g) and 4 molecular sieves (4 g) in dry tetrahydrofuran (50 ml) under nitrogen. The mixture was heated at 60° for 30 min then allowed to cool to room temperature. A solution of 2-amino-5-methoxybenzoic acid, methyl ester (2.0 g) in dry tetrahydrofuran (20 ml) was added and the mixture stirred at reflux for 2.5 h. The suspension was allowed to cool, filtered and the filtrate evaporated to give the title compound as a yellow solid (1.64 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05618827 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-de14df84f908491bba4e59f0038f2dee |
| Source note | uspto-grants-1997_04 |