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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1018975Erstellt: 25. Oktober 2026

Methanol → N-[(3R)-1-Azabicyclo[2.2.2]Oct-3-yl]4-Phenoxybenzamide

https://huagongshe.com/reaction/1018975

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt4-Phenoxybenzoic acidHCID 75182—
EduktDiphenyl chlorophosphateHCID 75654—
Edukt(3R)-1-Azabicyclo(2.2.2)octan-3-amineHCID 719215—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[(3R)-1-Azabicyclo[2.2.2]Oct-3-yl]4-PhenoxybenzamideHCID 783159576%

Reaktionsschritte

TEA (50 μL, 0.35 mmol) is added to a suspension of 4-phenoxybenzoic acid (75 mg, 0.35 mmol) in CH2Cl2 (1 mL). Diphenylchlorophosphate (62 μL, 0.3 mmol) is added and the resulting solution is stirred at room temperature for 30 minutes. A solution of (R)-3-aminoquinuclidine (1M in DMF, 0.2 mL, 0.2 mmol) is added and the resulting solution is stirred overnight at room temperature. MeOH is added and the mixture is poured through a column of AG50W×2 ion exchange resin (H+ form). The resin is washed with MeOH and then the product is eluted with 5% TEA in MeOH. The eluent is evaporated to dryness to yield the desired product (49 mg, 76%). MS for C20H22N2O2 (ESI) (M+H)+ m/z 323.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06486172B2
Quelldatensatzuspto-grants-2002_11
ORD IDord-5502a2cda01240918f32a318663e32b8
Quellennotizuspto-grants-2002_11