HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → N-(4-(5-Cyano-1-methyl-1H-pyrrol-2-yl)phenyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 5-(4-aminophenyl)-1-methyl-1H-pyrrole-2-carbonitrile | HCID 16050430 | — |
| Product | N-(4-(5-Cyano-1-methyl-1H-pyrrol-2-yl)phenyl)benzenesulfonamide | HCID 16050906 | — |
Reaction Steps
The title compound was prepared according to general procedure for sulfonylation of 5-(4-aminophenyl)-1-methyl-1H-pyrrole-2-carbonitrile using benzenesulfonyl chloride (70 μL, 0.55 mmol) to provide N-[4-(5-cyano-1-methyl-1H-pyrrol-2-yl)phenyl]benzene sulfonamide (0.046 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07291643B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-7a40c380453742368f5223b9472edfc8 |
| Source note | uspto-grants-2007_11 |