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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77009Generated: October 26, 2026

1-Hydroxybenzotriazole → (R)-Quinuclidin-3-yl 2-(4-fluorobenzylamino)-2-phenylacetate

https://huagongshe.com/reaction/77009

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Quinuclidinol, (-)-HCID 91404—
Reactant(4-Fluoro-benzylamino)-phenyl-acetic acid hydrochlorideHCID 67425426—
SolventAcetonitrileHCID 6342—
Product(R)-Quinuclidin-3-yl 2-(4-fluorobenzylamino)-2-phenylacetateHCID 5940110221%

Reaction Steps

A mixture of (4-fluoro-benzylamino)-phenyl-acetic acid hydrochloride (233 mg, 0.79 mmol), (R)-quinuclidin-3-ol (200 mg, 1.57 mmol), 2-(1H-benzo[d][1,2,3]triazol-1-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate(V) (596 mg, 1.57 mmol), TEA (0.22 mL, 1.57 mmol) and HOBT (241 mg, 1.57 mmol) in acetonitrile (10 mL) is stirred at RT for 48 hours. THF is removed under vacuum and the crude is partitioned between EtOAc and water. The organic phase is dried over sodium sulphate, filtered and evaporated to dryness. The crude is purified by preparative HPLC. The combined fractions are dried and partitioned between EtOAc and 2M K2CO3. The organic phase is dried over sodium sulphate, filtered and evaporated to dryness to achieve the title compound as colorless oil (61 mg, 21% yield, mixture of diastereoisomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835682B2
Source datasetuspto-grants-2014_09
ORD IDord-ae5add85318f48a489b0faa1aa081ebe
Source noteuspto-grants-2014_09