HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → HCID 10007831, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Tetrahydrofurane dichloromethane | HCID 21919333 | — |
| Reactant | HCID 44581620 | HCID 44581620 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10007831 | HCID 10007831 | — |
Reaction Steps
A mixture of 2-benzyloxy-5-chloro-[1,1′;2′,1″]terphenyl-2″-carboxylic acid (100 mg, 0.24 mmol), benzenesulphonamide (46 mg, 0.29 mmol), EDC (56 mg, 0.29 mmol), and 4-dimethylaminopyridine (5 mg, 0.03 mmol) in 1:1 dichloromethane/tetrahydrofuran (4 ml) was stirred at room temperature for 16 hours. The mixture was diluted with ethyl acetate (10 ml) and washed with aq. sodium bicarbonate (5 ml), dilute hydrochloric acid (5 ml), water (5 ml), and brine (5 ml). The organic phase was dried and evaporated. Purification by prep. HPLC gave the title compound. (27 mg 20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07446222B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-16cb7d8ff9d54875b649e03104922f7b |
| Source note | uspto-grants-2008_11 |