HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-acetyl-N-(5-amino-benzo[d]isothiazol-3-yl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Amino-5-nitrobenzisothiazole | HCID 158638 | — |
| Reactant | N-acetyl-N-(5-nitro-benzo[d]isothiazol-3-yl)-acetamide | HCID 21110339 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-acetyl-N-(5-amino-benzo[d]isothiazol-3-yl)-acetamide | HCID 21110338 | — |
Reaction Steps
N-acetyl-N-(5-nitro-benzo[d]isothiazol-3-yl)-acetamide (KRB01049): To a solution of 3-amino-5-nitrobenzisothiazole (1.00 g, 5.12 mmol) in DMF (20 mL) was added acetic anhydride (1 mL) and triethylamine (1 mL) and the resulting solution was stirred for 4 h. The yellow precipitate was filtered, washed quickly with cold ethyl acetate, and dried in vacuo (1.139 g, 80%). 1H NMR (CDCl3): δ 9.20 (1H, d, J=2.5 Hz), 8.87 (1H, d, J=9.4 Hz), 8.55 (1H, dd, J=9.4, 2.5 Hz), 2.69 (3H, s), 2.63 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07230020B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-3f0ccfe3275b4fee9ba9d415fcb41969 |
| Source note | uspto-grants-2007_06 |