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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1255015Erstellt: 25. Oktober 2026

Dicyclohexylcarbodiimide → (2-methoxy-phenylamino)-phenyl-acetic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)ester

https://huagongshe.com/reaction/1255015

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt3-Quinuclidinol, (-)-HCID 91404—
Edukt(2-Methoxy-phenylamino)-phenyl-acetic acid hydrochlorideHCID 67425641—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(2-methoxy-phenylamino)-phenyl-acetic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)esterHCID 46840572116,8%

Reaktionsschritte

PS-DCC (2.05 g, 2.57 mmol, loading: 1.25 mmol/g) is suspended in THF (15 mL) and shaken for few minutes. Then (2-methoxy-phenylamino)-phenyl-acetic acid hydrochloride (I36) (377 mg, 1.28 mmol) and HOBT (393 mg, 2.57 mmol) are added. After 10 minutes, (R)-quinuclidin-3-ol (490 mg, 3.85 mmol) is added and the mixture is shaken at RT for 16 hours (Conversion complete by UPLC/MS-UV). PS-DCC is filtered off and the filtrate is evaporated to dryness. The residue is dissolved in EtOAc and washed with sat. NaHCO3, water and brine. The organic layer is recovered, dried over Na2SO4, filtered and evaporated to afford the title compound as a yellow oil (548 mg, quantitative yield, mixture of diastereoisomers).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08455646B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-608c20ced0f94d57904956e6697d3256
Quellennotizuspto-grants-2013_06