HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 1-(4-Aminomethylbenzenesulfonyl)piperidine-4-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1-(4-Cyanobenzenesulfonyl)piperidine-4-carboxylic acid ethyl ester | HCID 3854242 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Aminomethylbenzenesulfonyl)piperidine-4-carboxylic acid ethyl ester | HCID 69157733 | 77% |
Reaction Steps
[Step 2] To a mixture of 1-(4-cyanobenzenesulfonyl)piperidine-4-carboxylic acid ethyl ester (1.36 g) in ethanol (84 ml) and tetrahydrofuran (14 ml) was added 28% aqueous ammonia (3 ml) and then Raney nickel (500 mg) was added. Under a hydrogen pressure (0.5 Mpa), the mixture was stirred at room temperature for 2 hrs., and undesired substances were removed by filtration. The filtrate was concentrated under reduced pressure to give 1-(4-aminomethylbenzenesulfonyl)piperidine-4-carboxylic acid ethyl ester (1.05 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07402595B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-e56ebbc421664cd19e0d9cbb2970ebae |
| Source note | uspto-grants-2008_07 |