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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888111Generated: October 26, 2026

(R)-3-((tert-butoxycarbonyl)amino)butanoic acid → tert-Butyl(R)-4-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-4-oxobutan-2-ylcarbamate

https://huagongshe.com/reaction/1888111

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-3-((tert-butoxycarbonyl)amino)butanoic acidHCID 2761507—
Reactant(S)-4-(4-chlorophenyl)-3,3-dimethylpiperidin-4-olHCID 18437142—
Producttert-Butyl(R)-4-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-4-oxobutan-2-ylcarbamateHCID 59444245—

Reaction Steps

tert-Butyl(R)-4-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-4-oxobutan-2-ylcarbamate was prepared from (S)-4-(4-chlorophenyl)-3,3-dimethylpiperidin-4-ol and Boc-D-beta-homoalanine using the conditions described in Example 1, Step 2. MS (ESI+)=425.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501782B2
Source datasetuspto-grants-2013_08
ORD IDord-0a9617b836ba4f8d97437b95874f3181
Source noteuspto-grants-2013_08