HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-tert-butylpiperidine-4-carboxamide → HCID 86706545, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-tert-butylpiperidine-4-carboxamide | HCID 7175833 | — |
| Reactant | 3-METHOXY-5-NITROBENZALDEHYDE | HCID 12137088 | — |
| Reactant | HCID 86706546 | HCID 86706546 | — |
| Product | HCID 86706545 | HCID 86706545 | — |
Reaction Steps
The title compound is prepared according to the reactions described for BB-5 above starting from 3-methoxy-5-nitro-benzaldehyde and piperidine-4-carboxylic acid tert-butylamide yielding after reductive amination 1-(3-methoxy-5-nitro-benzyl)-piperidine-4-carboxylic acid tert-butylamide; LC-MS A: tR=0.63 min; [M+H]+=350.14 followed by reduction with stannous chloride the title compound; LC-MS A: tR=0.50 min; [M+H]+=320.19.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428456B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-c6e2b715217d464a9f4ae3074143943d |
| Source note | uspto-grants-2016_08 |