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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77002Generated: October 27, 2026

Dicyclohexylcarbodiimide → HCID 58556953, compound

https://huagongshe.com/reaction/77002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Quinuclidinol, (-)-HCID 91404—
Reactant[(4-Fluoro-phenyl)-methyl-amino]-phenyl-acetic acid hydrochlorideHCID 67124664—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58556953HCID 5855695384%

Reaction Steps

PS-DCC (1.02 g, 1.35 mmol, loading: 1.33 mmol/g) is suspended in dry THF (13.5 mL). Then HOBT (0.21 g, 1.35 mmol), [(4-fluoro-phenyl)-methyl-amino]-phenyl-acetic acid hydrochloride (I71) (0.20 g, 0.68 mmol) and (R)-quinuclidin-3-ol (0.26 g, 2.03 mmol) are added. The mixture is shaken at RT overnight. PS-DCC is filtered off, washed with EtOAc and THF. The solution is evaporated and the residue is portioned between EtOAc and water. The organic phase is washed with sat. NaHCO3, dried (Na2SO4) and evaporated. The crude is purified by flash chromatography (DCM/MeOH=95/5) to afford the title compound as a colorless oil (209 mg, 84% yield, mixture of diastereoisomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835682B2
Source datasetuspto-grants-2014_09
ORD IDord-6c8ea732153e4d1d917f42becab5d028
Source noteuspto-grants-2014_09