HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide → 4-amino-3-isopropoxy-N-(1-methyl-piperidin-4-yl)-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide | HCID 67076401 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-amino-3-isopropoxy-N-(1-methyl-piperidin-4-yl)-benzamide | HCID 58014999 | 95.3% |
Reaction Steps
To a solution of 1.2 g (3.6 mmole) of 3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide in 25 mL of methanol was added 0.12 g of 10% palladium on carbon. The hydrogenation reaction was carried out under 50 psi of hydrogen for 2 hours. The mixture was filtered, concentrated under reduced pressure and triturated with ether. The solid was collected by filtration, washed with ether and dried under vacuum to give 1.0 g of 4-amino-3-isopropoxy-N-(1-methyl-piperidin-4-yl)-benzamide as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08003785B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-695d0ef61d084dc6ab4ef81caf607ec8 |
| Source note | uspto-grants-2011_08 |