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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344293Generated: October 29, 2026

cis-4-Azidomethyl-1-tert-butoxycarbonyl-3-methoxypiperidine → tert-Butyl (3S,4R)-4-(aminomethyl)-3-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/344293

Reaction equation

Participants

RoleNameHCIDCharge
Reactantcis-4-Azidomethyl-1-tert-butoxycarbonyl-3-methoxypiperidineHCID 86753637—
CatalystHCID 178420936HCID 178420936—
SolventMethanolHCID 887—
Producttert-Butyl (3S,4R)-4-(aminomethyl)-3-methoxypiperidine-1-carboxylateHCID 7007467788.5%

Reaction Steps

To a solution of cis-4-azidomethyl-1-tert-butoxycarbonyl-3-methoxypiperidine (1.5 g) in methanol (50 ml) was added 20% palladium carbon hydroxide (0.6 g), and the resulting mixture was stirred at room temperature under hydrogen atmosphere for 2 hr. 20% Palladium carbon hydroxide was filtered off and the solvent was evaporated under reduced pressure to give 1.2 g of cis-4-aminomethyl-1-tert-butoxycarbonyl-3-methoxypiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05864039
Source datasetuspto-grants-1999_01
ORD IDord-d48448f9f14e4c21a299ed8e1280016a
Source noteuspto-grants-1999_01