HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(3,4-dichlorophenyl)-3-nitro-2-piperid-1-yl-5-trifluoromethylbenzamide → 3-amino-N-(3,4-dichlorophenyl)-2-piperid-1-yl-5-trifluoromethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(3,4-dichlorophenyl)-3-nitro-2-piperid-1-yl-5-trifluoromethylbenzamide | HCID 11854386 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-amino-N-(3,4-dichlorophenyl)-2-piperid-1-yl-5-trifluoromethylbenzamide | HCID 11854387 | — |
Reaction Steps
To a solution of N-(3,4-dichlorophenyl)-3-nitro-2-piperid-1-yl-5-trifluoromethylbenzamide, Example 1 (4.15 g) in THF (80 ml), is added Raney nickel (2 g) under nitrogen. The reaction medium is hydrogenated at room temperature under a pressure of 45 bar. At the end of the reaction (stable absorption of hydrogen), the catalyst is removed and the medium is concentrated. 3.15 g of 3-amino-N-(3,4-dichlorophenyl)-2-piperid-1-yl-5-trifluoromethylbenzamide are obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947675B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-37b0814788a54c7a81a18fd1af91ac7d |
| Source note | uspto-grants-2011_05 |