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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1255018Erstellt: 25. Oktober 2026

Dicyclohexylcarbodiimide → phenyl-(3-trifluoromethoxy-phenylamino)-acetic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)ester

https://huagongshe.com/reaction/1255018

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt3-Quinuclidinol, (-)-HCID 91404—
EduktPhenyl-(3-trifluoromethoxy-phenylamino)-acetic acid hydrochlorideHCID 67426283—
LösungsmittelTetrahydrofuranHCID 8028—
Produktphenyl-(3-trifluoromethoxy-phenylamino)-acetic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)esterHCID 5940121286%

Reaktionsschritte

PS-DCC (920 mg, 1.15 mmol, loading: 1.25 mmol/g) is suspended in THF (15 mL). Phenyl-(3-trifluoromethoxy-phenylamino)-acetic acid hydrochloride (I40) (200 mg, 0.57 mmol) and HOBT (176 mg, 1.15 mmol) are added, followed by (R)-quinuclidin-3-ol (219 mg, 1.73 mmol) and the mixture is shaken for 16 hours at RT. PS-DCC is filtered off and the filtrate is evaporated. The resulting residue is dissolved in EtOAc and washed with water, sat. NaHCO3, water and brine. The organic phase is dried over Na2SO4, filtered and evaporated to give the title compound as a colorless oil (206 mg, 85% yield, mixture of diastereoisomers).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08455646B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-a384c87d74e246f396fff8d21f9ae1d5
Quellennotizuspto-grants-2013_06