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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949085Generated: November 2, 2026

4-tert-Butoxycarbonylamino-4-(4-isopropyl-phenylcarbamoyl)-piperidine-1-carboxylic acid benzyl ester → [4-(4-Isopropyl-phenylcarbamoyl)-piperidin-4-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1949085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-Butoxycarbonylamino-4-(4-isopropyl-phenylcarbamoyl)-piperidine-1-carboxylic acid benzyl esterHCID 66921386—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product[4-(4-Isopropyl-phenylcarbamoyl)-piperidin-4-yl]-carbamic acid tert-butyl esterHCID 6692134594%

Reaction Steps

A mixture of 2.84 g (6 mmol) 4-tert-Butoxycarbonylamino-4-(4-isopropyl-phenylcarbamoyl)-piperidine-1-carboxylic acid benzyl ester (example 82, step 1) in 80 mL methanol was hydrogenated with H2 over Pd/C (10%) for 2 h at room temperature. The mixture was filtered off and evaporated to dryness to yield 1.94 g (94%) of the title compound as off-white crystals. MS (m/e): 362.4 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399676B2
Source datasetuspto-grants-2013_03
ORD IDord-10fc16e31ec442ca8f7dfed152680ba4
Source noteuspto-grants-2013_03