HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonamide → HCID 23401735, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | HCID 23401732 | HCID 23401732 | — |
| Product | HCID 23401735 | HCID 23401735 | 89% |
Reaction Steps
4-chloro-N-(5-chloro-2-fluorophenyl)-N-[4-[(methylsulfonyl)amino]-1(R)-methylbutyl]-benzenesulfonamide was prepared analogous to 4-chloro-N-(2,5-dichlorophenyl)-N-[4-[[4 (methylsulfonyl)methyl]-1-piperidinyl]-1(R)-methylbutyl]benzenesulfonamide by reacting 4-chloro-N-(5-chloro-2-fluorophenyl)-N-[4-bromo-1(R)-methylbutyl]benzenesulfonamide with methanesulfonamide. Yield=89%; MS (ESI+), 483 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06967196B1 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-0ff03de05859448998b99c8dc800525a |
| Source note | uspto-grants-2005_11 |