HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(5-aminoacetylamino-4-nitro-2-phenoxyphenyl)methanesulfonamide → N-[5-(n-butylaminoacetylamino)4-nitro-2-phenoxyphenyl]methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(5-aminoacetylamino-4-nitro-2-phenoxyphenyl)methanesulfonamide | HCID 22406110 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[5-(n-butylaminoacetylamino)4-nitro-2-phenoxyphenyl]methanesulfonamide | HCID 15285982 | — |
Reaction Steps
Following the same procedure as that of Example 23 except for the use of N-(5-aminoacetylamino-4-nitro-2-phenoxyphenyl)methanesulfonamide obtained by the procedure of Example 22 andacetonitrile in place of N-[5-(n-butylaminoacetylamino)-4-nitro-2-phenoxyphenyl]methanesulfonamide and acetone as a reaction solvent used in Example 23, N-(5-aminoacetylamino-4-nitro-2-phenoxyphenyl)methanesulfonamide hydrochloride was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521311 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-cf9cb1ba9250485a96aa7cf5b8dc1fe1 |
| Source note | uspto-grants-1996_05 |