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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874838Generated: October 30, 2026

3-Aminobenzyl alcohol → (R)-Quinuclidin-3-yl ((S)-(3-(2-((3-(hydroxymethyl)phenyl)amino)-2-oxoethoxy)phenyl)(phenyl)methyl)carbamate

https://huagongshe.com/reaction/874838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminobenzyl alcoholHCID 80293—
Reactant4-((3-((S)-Phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)-phenoxy)methyl)benzoic acidHCID 86720815—
Reactant2-(3-((S)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)-methyl)phenoxy)acetic acidHCID 90198139—
Product(R)-Quinuclidin-3-yl ((S)-(3-(2-((3-(hydroxymethyl)phenyl)amino)-2-oxoethoxy)phenyl)(phenyl)methyl)carbamateHCID 90203069—

Reaction Steps

The title compound was prepared as described in Example 1 Step 11 with 3-aminobenzyl alcohol and 2-(3-((S)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)-methyl)phenoxy)acetic acid replacing 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. Crude material used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980913B2
Source datasetuspto-grants-2015_03
ORD IDord-e7be00599826402191bd6b30c57676b1
Source noteuspto-grants-2015_03