HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → N-[4-(3-amino-phenyl)-thiazol-2-yl]-4-methyl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | 4-Methyl-N-[4-(3-nitro-phenyl)-thiazol-2-yl]-benzenesulfonamide | HCID 4233969 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[4-(3-amino-phenyl)-thiazol-2-yl]-4-methyl-benzenesulfonamide | HCID 21845567 | 79.7% |
Reaction Steps
A solution of 1.5 g of 4-methyl-N-[4-(3-nitro-phenyl)-thiazol-2-yl]-benzenesulfonamide in 150 ml of methanol and 70 ml of ethyl acetate was hydrogenated at room temperature after the addition of 0.15 g of palladium on active charcoal (10%). The catalyst was filtered off and the filtrate was concentrated. Crystallization from ethyl acetate/hexane (1:1) yielded 1.1 g of N-[4-(3-amino-phenyl)-thiazol-2-yl]-4-methyl-benzenesulfonamide as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05877193 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-4e3219a023054055b13884b71cf78be1 |
| Source note | uspto-grants-1999_03 |