HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(2,3-Dimethoxy-7-nitro-quinoxalin-5-ylmethyl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Aminomethyl-2,3-dimethoxy-7-nitro-quinoxaline | HCID 17915296 | — |
| Reactant | 5-Bromomethyl-7-nitro-2,3-dimethoxyquinoxaline | HCID 23297983 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Diethylformamide | HCID 12051 | — |
| Product | N-(2,3-Dimethoxy-7-nitro-quinoxalin-5-ylmethyl)-acetamide | HCID 18706427 | — |
Reaction Steps
111 mg (0.437 mmol) of 5-aminomethyl-2,3-dimethoxy-7-nitro-quinoxaline, obtainable in a manner analogous to that described in Example 9 but starting from 5-bromomethyl-2,3-dimethoxy-7-nitro-quinoxaline, are stirred with 0.046 ml (1.1 equiv.) of acetic anhydride and 0.073 ml (1.2 equiv.) of triethylamine in 5 ml of N,N-diethylformamide at room temperature for 24 hours. The reaction mixture is diluted with diethyl ether, and the solid is filtered off, washed with diethyl ether and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06080743 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-390f1566680049a9818d0fcf93d57184 |
| Source note | uspto-grants-2000_06 |