HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Cyclopropylmethyl)-1-(ethylsulfonyl)piperidine-4-carbonitrile → 1-[4-(Cyclopropylmethyl)-1-(ethylsulfonyl)piperidin-4-yl]methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Cyclopropylmethyl)-1-(ethylsulfonyl)piperidine-4-carbonitrile | HCID 59428186 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ammonia methanol | HCID 21705897 | — |
| Product | 1-[4-(Cyclopropylmethyl)-1-(ethylsulfonyl)piperidin-4-yl]methanamine | HCID 68620156 | — |
Reaction Steps
A solution of 4-(cyclopropylmethyl)-1-(ethylsulfonyl)piperidine-4-carbonitrile (I-4, 3.1 mg, 11.1 mmol) in 2 M NH3/MeOH (50 mL) was treated with excess Raney Ni and agitated under an atmosphere of H2 (40 psi) in a Parr apparatus. After 5 h, the reaction was filtered through Celite (MeOH wash) and concentrated under reduced pressure to afford 1-[4-(cyclopropylmethyl)-1-(ethylsulfonyl)-piperidin-4-yl]methanamine (I-5, M+H+=261.2) as a yellow oil. This material was used in subsequent reactions without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776886B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-09d675b5db4d4b7c8294c54422a51ea9 |
| Source note | uspto-grants-2010_08 |