HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Methoxybenzo[d]isothiazole-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Methoxybenzisothiazole-3-carboxamide | HCID 66636470 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Methoxybenzo[d]isothiazole-3-carboxylic acid | HCID 66636805 | 89% |
Reaction Steps
To a solution of the amide (5.46 mmol) in methanol (100 mL) was added 10 N sodium hydroxide (12 mL). The mixture was heated at reflux for 12 h, cooled to rt, and was acidified to pH <2 by the slow addition of conc. hydrochloric acid. The organic layer was extracted with dichloromethane (2×) and was dried over sodium sulfate. The crude product was purified by chromatography (300/50/1 dichloromethane/methanol/formic acid) to provide 6-methoxy-1,2-benzisothiazole-3-carboxylic acid (89%) as a pink solid. The acid was coupled with 1,4-diazabicyclo[3.2.2]nonane according to procedure A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07632831B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-4c76bb4c441b440da89aff4ea820b665 |
| Source note | uspto-grants-2009_12 |