HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl 4-(carbamoylamino)-3-nitrobenzene-1-sulfonate → 5-Phenoxysulfonyl-2-ureidoaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl 4-(carbamoylamino)-3-nitrobenzene-1-sulfonate | HCID 15585382 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 5-Phenoxysulfonyl-2-ureidoaniline | HCID 15585526 | — |
Reaction Steps
33.7 g of 5-phenoxysulfonyl-2-ureidonitrobenzene in 250 ml of methanol and 250 ml of 2-methoxyethanol are hydrogenated under normal pressure with a catalytic amount of Raney nickel. After uptake of hydrogen is complete, the catalyst is filtered off with suction, washed with dimethylformamide and the solution is evaporated under reduced pressure, induced to crystallize with methanol, and the crystals are filtered off with suction and washed with methanol, melting point 180° C., decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04504490 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-71d78577a479446cb5eeb5b16ab49657 |
| Source note | uspto-grants-1985_03 |