HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (S)-2-(1-methylethylsulfonamido)-N-(2-(methylsulfonamido)phenyl)-2,3-dihydro-1H-indene-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(2-aminophenyl)methanesulfonamide | HCID 241357 | — |
| Reactant | (S)-2-(1-methylethylsulfonamido)-2,3-dihydro-1H-indene-5-carbonyl chloride | HCID 86668751 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-2-(1-methylethylsulfonamido)-N-(2-(methylsulfonamido)phenyl)-2,3-dihydro-1H-indene-5-carboxamide | HCID 66736340 | 28.6% |
Reaction Steps
A mixture of triethylamine (0.083 mmol, 0.012 mL, 8.38 mg) and N-(2-aminophenyl)methanesulfonamide (0.083 mmol, 15.43 mg) in DCM (2 mL) was added to a solution of (S)-2-(1-methylethylsulfonamido)-2,3-dihydro-1H-indene-5-carbonyl chloride (0.083 mmol, 25 mg) in DCM (1 mL) was added. The reaction mixture was stirred at room temp overnight. H2O was added and the reaction mixture filtered through a hydrophobic frit and the DCM layer was concentrated under reduced pressure. The residue was purified by prep-HPLC to give desired product (10.7 mg, 28.6%). MS (ESI): m/z [M−H]− 450.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633237B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-25b2277f54a14d6db35d1545468b4e04 |
| Source note | uspto-grants-2014_01 |