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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43496Generated: October 29, 2026

Tert-butyl cis(+/-)-3-(4-{[(benzyloxy)carbonyl]amino}-3-ethoxypiperidin-1-yl)benzoate → tert-Butyl cis(+/-)-3-(4-amino-3-ethoxypiperidin-1-yl)benzoate

https://huagongshe.com/reaction/43496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl cis(+/-)-3-(4-{[(benzyloxy)carbonyl]amino}-3-ethoxypiperidin-1-yl)benzoateHCID 131730856—
CatalystHCID 178418390HCID 178418390—
Producttert-Butyl cis(+/-)-3-(4-amino-3-ethoxypiperidin-1-yl)benzoateHCID 86648508—

Reaction Steps

The same operation as in Example (40e) was performed using tert-butyl cis(±)-3-(4-{[(benzyloxy)carbonyl]amino}-3-ethoxypiperidin-1-yl)benzoate obtained in Example (48d) (100 mg, 0.22 mmol) and a 10% palladium-carbon catalyst (40 mg) to obtain the title compound. The resulting compound was used for the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-78de4d5aa6e44d29b3e19f00c2297b57
Source noteuspto-grants-2013_09