HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 7-nitro-2,3-dihydro-1H-Benz[de]isoquinoline-6-sulfonic acid amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 7-nitro-2,3-dihydro-2-trifluoroacetyl-1H-Benz[de]isoquinoline-6-sulfonyl chloride | HCID 21189601 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-nitro-2,3-dihydro-1H-Benz[de]isoquinoline-6-sulfonic acid amide | HCID 20666115 | — |
Reaction Steps
A 2M solution of ammonia in methanol (10 mL) is added to a solution of 7-nitro-2,3-dihydro-2-trifluoroacetyl-1H-Benz[de]isoquinoline-6-sulfonyl chloride (4 mmol) in 40 mL of methanol and the resulting mixture is stirred at room temperature for 24 hours. The mixture is then concentrated under vacuum and the residue is partitioned between ethyl acetate and water. The organic layer is dried over magnesium sulfate and concentrated to afford the title compound. The crude product can be purified by recrystallization or chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251890B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-b19702fd44c944df9e8d83ea943b91d7 |
| Source note | uspto-grants-2001_06 |