HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(6-nitro-2,3-dioxo-1,2,3,4,7,8,9,10-octahydro-benzo[f]quinoxalin-9-yl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 9-Amino-6-nitro-1,4,7,8,9,10-hexahydro-benzo[f]quinoxaline-2,3-dione | HCID 19696204 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(6-nitro-2,3-dioxo-1,2,3,4,7,8,9,10-octahydro-benzo[f]quinoxalin-9-yl)-acetamide | HCID 19696211 | 88% |
Reaction Steps
A mixture of 9-amino-6-nitro-1,4,7,8,9,10-hexahydro-benzo[f]quinoxaline-2,3-dione (0.15 g, 0.5 mmol), acetic anhydride (0.1 g, 1 mmol) and triethylamine (0.2 g, 2 mmol) in dimethylformamide (5 mL) was stirred at room temperature for 3 h. The solvent was removed by rotoevaporation, and the residue suspended in water and 2N HCl. The solid which formed was collected by filtration, washed with diethyl ether and dried to give the acetamide (0.14 g) in 88% yield. Anal. calc'd for C14H14N4O5.H2O: C, 50.00; H, 4.80; N, 16.66; found-C, 49.92; H, 4.77; N, 16.04.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05721234 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-3d95a8f8165846d785da2d3bb0834cfe |
| Source note | uspto-grants-1998_02 |