HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[5-(3-{4-[(2-methylpropyl)sulfonyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 1-Propanesulfonyl chloride, 2-methyl- | HCID 182236 | — |
| Reactant | N-{5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide | HCID 57843497 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[5-(3-{4-[(2-methylpropyl)sulfonyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide | HCID 57843393 | 20% |
Reaction Steps
To a solution of N-{5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide (0.20 mmol) and triethylamine (0.20 mmol) in dichloromethane (2 ml) was added a sulfonyl chloride such as 2-methyl-1-propanesulfonyl chloride (0.22 mmol). The reaction stirred for 18 hours at ambient temperature and purified on silica by column chromatography (80% ethyl acetate/hexanes). The desired fractions were combined and concentrated to give the title compound (22 mg, 20%) as an off-white solid. MS(ES)+ m/e 567.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592342B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-e54585a1fdf44512b5607e9217bb1aa0 |
| Source note | uspto-grants-2009_09 |