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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874835Generated: October 30, 2026

4-((3-((S)-Phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)-phenoxy)methyl)benzoic acid → (R)-Quinuclidin-3-yl((S)-(3-((1-(4-formylbenzoyl)piperidin-4-yl)methoxy)phenyl)(phenyl)methyl)carbamate

https://huagongshe.com/reaction/874835

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((3-((S)-Phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)-phenoxy)methyl)benzoic acidHCID 86720815—
Reactant4-Formyl benzoic acid 3-(1,3-dioxolan-2-yl)propyl piperidine-4-carboxylate hydrochlorideHCID 90198193—
Reactant(R)-quinuclidin-3-yl((S)-phenyl(3-(piperidin-4-ylmethoxy)phenyl)methyl)carbamateHCID 90210005—
Product(R)-Quinuclidin-3-yl((S)-(3-((1-(4-formylbenzoyl)piperidin-4-yl)methoxy)phenyl)(phenyl)methyl)carbamateHCID 90203159—

Reaction Steps

The title compound was prepared as described in Example 1 Step 11 with (R)-quinuclidin-3-yl((S)-phenyl(3-(piperidin-4-ylmethoxy)phenyl)methyl)carbamate and 4-formyl benzoic acid 3-(1,3-dioxolan-2-yl)propyl piperidine-4-carboxylate hydrochloride and 4-((3-((S)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoic acid respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980913B2
Source datasetuspto-grants-2015_03
ORD IDord-8e99a79dd4854e1eadaa029952f65e38
Source noteuspto-grants-2015_03