HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → 1-(2-Chlorobenzyl)-3-(1-hydroxyiminoethyl)-2-propylindole-6-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-Acetyl-1-(2-chlorobenzyl)-2-propylindole-6-carboxamide | HCID 10155921 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(2-Chlorobenzyl)-3-(1-hydroxyiminoethyl)-2-propylindole-6-carboxamide | HCID 56990785 | 86.1% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a suspension of 3-acetyl-1-(2-chlorobenzyl)-2-propylindole-6-carboxamide (36.5 mg) in ethanol (5 ml) was added hydroxylamine hydrochloride (70 mg) and sodium acetate (200 mg), and the mixture was heated in a sealed tube at 100° C. The reaction was evaporated in vacuo, then the residue was diluted with ethyl acetate and washed with water and brine. The organic phase was dried over sodium sulfate and evaporated in vacuo. The residue was triturated with diisopropyl ether to give 1-(2-chlorobenzyl)-3-(1-hydroxyiminoethyl)-2-propylindole-6-carboxamide (32.7 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06069156 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-11a9a403f247433cad2a8b8efa525c46 |
| Source note | uspto-grants-2000_05 |