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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353342Generated: October 25, 2026

trans-1-Boc-4-aminomethyl-3-hydroxypiperidine → HCID 11015727, compound

https://huagongshe.com/reaction/353342

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttrans-1-Boc-4-aminomethyl-3-hydroxypiperidineHCID 11075229—
ReactantHCID 88040818HCID 88040818—
SolventAcetonitrileHCID 6342—
ProductHCID 11015727HCID 1101572780%

Reaction Steps

A mixture of intermediate (1-e) (0.087 mol) and intermediate (3-a) (0.087 mol) in acetonitrile (600 ml) was stirred and refluxed for 90 min. The reaction mixture was cooled, and the solvent was evaporated. The residue was partitioned between DCM and water. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was suspended in DIPE with a drop of ACN, filtered off and dried (vacuum, 40° C.), yielding 30.3 g (80%) of (±)-1,1-dimethylethyl trans-4-[[(4-amino-5-chloro-2,3-dimethoxybenzoyl)amino]methyl]-3-hydroxy-1-piperidinecarboxylate (interm. 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750349B2
Source datasetuspto-grants-2004_06
ORD IDord-f649c2ede5634f988e45339bcfac2953
Source noteuspto-grants-2004_06