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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486709Generated: November 1, 2026

N-tert-butylpiperidine-4-carboxamide → HCID 86706545, compound

https://huagongshe.com/reaction/1486709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-tert-butylpiperidine-4-carboxamideHCID 7175833—
Reactant3-METHOXY-5-NITROBENZALDEHYDEHCID 12137088—
ReactantHCID 86706546HCID 86706546—
ProductHCID 86706545HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428456B2
Source datasetuspto-grants-2016_08
ORD IDord-c6e2b715217d464a9f4ae3074143943d
Source noteuspto-grants-2016_08