HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → N-(5-aminoacetylamino-4-nitro-2-phenoxyphenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | N-(4-nitro-2-phenoxy-5-phthalimidoacetylaminophenyl)methanesulfonamide | HCID 22406108 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | N-(5-aminoacetylamino-4-nitro-2-phenoxyphenyl)methanesulfonamide | HCID 22406110 | 73.5% |
Reaction Steps
To 350 ml of a dichloromethane-methanol (5:2) solution containing 9.5 g of N-(4-nitro-2-phenoxy-5-phthalimidoacetylaminophenyl)methanesulfonamide was added 0.64 ml of 99% hydrazine monohydrate at room temperature, followed by stirring for 19 hours. The precipitate was removed by filtration, followed by washing with hot acetonitrile. The filtrate was washed with water, and concentrated under reduced pressere. The resulting precipitate was washed with ethanol and dried to give 5.2 g of N-(5-aminoacetylamino-4-nitro-2 -phenoxyphenyl)methanesulfonamide as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521311 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-a8948d2e22914161856ac9ca49e3a941 |
| Source note | uspto-grants-1996_05 |