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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 75408Erstellt: 25. Oktober 2026

Triethylamine → 3-(2-Chloropyrimidin-4-yl)-8-oxa-3-azabicyclo[3,2,1]octane

https://huagongshe.com/reaction/75408

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2,4-DichloropyrimidineHCID 77531—
Edukt8-Oxa-3-aza-bicyclo(3.2.1)octane hydrochlorideHCID 21983536—
LösungsmittelEthanolHCID 702—
Produkt3-(2-Chloropyrimidin-4-yl)-8-oxa-3-azabicyclo[3,2,1]octaneHCID 6637152789%
Produkt3-(4-Chloro-pyrimidin-2-yl)-8-oxa-3-aza-bicyclo[3.2.1]octaneHCID 866658784%

Reaktionsschritte

A 745 mg (5 mmol) portion 2,4-dichloropyrimidine (1) was dissolved in 20 mL EtOH at 0 C. 8-oxa-3-aza-bicyclo[3.2.1]octane hydrochloride (2, 748 mg, 5 mmol) was added followed by the addition of NEt3 (2.1 mL, 15 mmol). The mixture was stirred for 1 hour at ambient temperature. The mixture was concentrated, dissolved in EtOAc and washed with saturated NaHCO3. The aqueous phase was extracted with EtOAc and the combined organic phases were dried (MgSO4), filtered and concentrated. The mixture was purified by silica gel chromatography (20-70% EtOAc in hexanes) to give 1,003 mg (4.4 mmol, 89%) of 3-(2-chloro-pyrimidin-4-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane (3) along with 50 mg (0.22 mmol, 4%) of 3-(4-chloro-pyrimidin-2-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane (4).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835429B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-42bc12a8e8aa4652ad482317cfda17d5
Quellennotizuspto-grants-2014_09