Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 67192604 | HCID 67192604 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 61113174 | HCID 61113174 | 100% |
Reaction Steps
1-(4-Nitro-benzenesulfonyl)-piperidine-4-carboxylic acid dimethylamide (0.17 g, 0.49 mmol) was suspended in a 5:1 mixture of ethanol and water (3 ml). To this solution was added iron powder (0.08 g, 0.98 mmol) followed by saturated ammonium chloride solution (0.1 ml) and the mixture was stirred at room temperature for 18 hours. After this time, the reaction mixture was filtered through a pad of celite, the celite was washed with ethanol (10 ml) and ethyl acetate (50 ml) and the solution was concentrated under vacuum. The resulting residue was partitioned between DCM (50 ml) and water (20 ml), the organic layer was separated, dried with MgSO4, filtered and concentrated to afford the title compound (0.15 g, 100% yield) as a yellow solid. Tr=1.71 min, m/z (ES+) (M+H)+ 312.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946197B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-7bdacfb4059e4692a22f20bddb195c8f |
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| Source note | uspto-grants-2015_02 |
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