HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl cyanide → 4-{[Cyano(phenyl)methyl]amino}benzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 5877-53-2 | HCID 308405 | — |
| Product | 4-{[Cyano(phenyl)methyl]amino}benzene-1-sulfonamide | HCID 21862881 | — |
Reaction Steps
Following a procedure similar to that described in Example 1(ii), but using N-benzylidene-4-sulfamoylaniline [prepared as described in step (i) above] and trimethylsilyl cyanide as starting materials, the title compound was obtained as a slightly yellow powder (yield 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05908858 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-29dd4e5eb61c40a3bc5f61d16548891a |
| Source note | uspto-grants-1999_06 |