HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 44391097, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 2,4-Dichlorobenzoyl chloride | HCID 66645 | — |
| Reactant | 1-Benzofuran-6-sulfonamide | HCID 19807329 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 44391097 | HCID 44391097 | — |
Reaction Steps
To a solution of benzofuran-6-sulfonamide (120 mg, 0.608 mmol) in CH2Cl2 (3.6 mL) and pyridine (2.3 mL) is added DMAP (75 mg, 0.611 mmol) and 2,4-dichlorobenzoyl chloride (153 mg, 0.730 mmol) and the reaction is stirred at room temperature overnight. The reaction mixture is diluted with CH2Cl2 then washed with 2 M HCl (2×) and dried (MgSO4). The organic solution is filtered and evaporated under vacuum to give the crude product. Flash chromatography on silica gel eluting with a gradient {CH2Cl2to CH2Cl2:(CHCl3:MeOH) [4:1(9:1)]} gives the title compound as a tan solid. ES(−)MS m/z 368, (M−H)− consistent with 2 Cl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07282595B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-96b4729fdf1844b09405ffc7025ddf02 |
| Source note | uspto-grants-2007_10 |