HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → HCID 22099489, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | HCID 22099399 | HCID 22099399 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22099489 | HCID 22099489 | 60.9% |
Reaction Steps
To a mixture of 680 mg of 2-{[4-(4-nitrophenyl)piperazin-1-yl]carbonylamino}-4-methoxy-6-tert-butylphenol hydrochloride, 30 ml of methanol and 30 ml of dioxane was added 100 mg of 10% palladium-carbon (Pd-C). The mixture was subjected to catalytic reduction for 4 hours by using a Parr's reduction apparatus. After removing the catalyst by filtration, the filtrate was condensed. The residue was dissolved in 10 ml of dichloromethane, and after adding 1 ml of 4N hydrogen chloride-dioxane solution, the mixture was treated with an activated charcoal. The treated mixture was evaporated to dryness under reduced pressure to give 210 mg of 2-{[4-(4-aminophenyl)piperazin-1-yl]carbonylamino}-4-methoxy-6-tert-butylphenol dihydrochloride as powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05849732 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-1766d1bff4f94005a9649eb3b439dc2f |
| Source note | uspto-grants-1998_12 |