HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → 6-[2-(3-Benzoylphenyl)propionylsulfamoyl]hexanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Ketoprofen | HCID 3825 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 848432-25-7 | HCID 58871553 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-[2-(3-Benzoylphenyl)propionylsulfamoyl]hexanoic acid | HCID 11224210 | 46.3% |
Reaction Steps
To a suspension of racemic ketoprofen (3.81 g, 15.0 mmol) in dichloromethane (50 ml) were added HOAt (2.04 g, 15.0 mmol) and EDC (2.88 g, 15.0 mmol), and the mixture was stirred until a clear solution resulted. To this solution was added a solution of 6-sulfamoylhexanoic acid ethyl ester (2.23 g, 10.0 mmol) and DI PEA (2.56 ml) in dichloromethane, and the mixture was stirred at room temperature for 3 d. The mixture was washed with 1N aqueous HCl, dried over MgSO4, and concentrated. Purification by column chromatography yielded 2.0 g (44%) of the title compound. An analytical sample was obtained by preparative HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897560B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-3cfeb6da15b64c9a846fa6eddc2f2007 |
| Source note | uspto-grants-2011_03 |