HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonamide → HCID 23401685, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | HCID 23401683 | HCID 23401683 | — |
| Product | HCID 23401685 | HCID 23401685 | 81% |
Reaction Steps
4-chloro-N-(2,5-dichlorophenyl)-N-[4-[[(benzyloxy)carbonyl]amino]-1(R)-methylbutyl]-benzenesulfonamide was prepared analogous to 4-chloro-N-[2,5-dichlorophenyl]-N-[(R)-1-methyl-4-(acetylamino)butyl]benzenesulfonamide by reacting 4-chloro-N-[2,5-dichlorophenyl]-N-[R]-1-methyl-4-aminobutyl]benzenesulfonamide with benzyl chloroformate. Yield=81%; MS (ESI+), 555 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06967196B1 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-44b4451b037040d19e0e3c0649e9b240 |
| Source note | uspto-grants-2005_11 |