HuagongsheHuagongshe Chemistry Print Report · For research reference only
Succinic anhydride → N-(2,3-Dimethoxy-7-nitro-quinoxalin-5-ylmethyl)-succinic acid amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Aminomethyl-2,3-dimethoxy-7-nitro-quinoxaline | HCID 17915296 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | N-(2,3-Dimethoxy-7-nitro-quinoxalin-5-ylmethyl)-succinic acid amide | HCID 70272034 | — |
Reaction Steps
55 μl (0.397 mmol) of triethylamine and 40 mg (0.397 mmol) of succinic anhydride are added to a suspension of 100 mg (0.378 mmol) of 5-aminomethyl-2,3-dimethoxy-7-nitro-quinoxaline in 2 ml of tert-butyl methyl ether and the mixture is stirred for 3 hours at room temperature. The mixture is then filtered and the residue is washed twice with tert-butyl methyl ether. The filter residue is chromatographed on silica gel with dichloromethane/methanol/acetic acid (95:4.5:0.5). The title compound is obtained in the form of a beige powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06080743 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-537b3ffc34ed46dc9454a2629976c075 |
| Source note | uspto-grants-2000_06 |