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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2169184Erstellt: 27. Oktober 2026

Phosphorus oxychloride → HCID 178464493, Verbindung

https://huagongshe.com/reaction/2169184

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphorus oxychlorideHCID 24813—
EduktDry ice ethyleneglycolHCID 86601574—
EduktN-(2-(tert-butyldimethylsilyloxy)ethyl)-1,1,1-trifluoropropan-2-amineHCID 86725834—
EduktHCID 178524871HCID 178524871—
LösungsmittelWaterHCID 962—
LösungsmittelPyridineHCID 1049—
ProduktHCID 178464493HCID 17846449358,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 5-(benzyloxy)-2-((1-(4-chlorophenyl)cyclopentyl)methyl)-6-hydroxypyrimidine-4-carboxylic acid (28-02) (150 mg, 342 μmol, Eq: 1.00) and N-(2-(tert-butyldimethylsilyloxy)ethyl)-1,1,1-trifluoropropan-2-amine (41) (102 mg, 376 μmol, Eq: 1.1) in pyridine (1.5 ml) was added POCl3 (157 mg, 95.6 μl, 1.03 mmol, Eq: 3.00) at −10° C. (ethylene glycol-dry-ice bath), then the reaction mixture was stirred at 0° C. for 2 hr. Ice cooled-water was slowly added to the reaction mixture at 0° C., which was extracted with ethyl acetate. The organic layer was washed with aqueous saturated NaHCO3 solution, dried (MgSO4), concentrated, and chromatographed (silica gel, gradient 5 to 50% ethyl acetate-hexane) to obtain 5-(benzyloxy)-N-(2-(tert-butyldimethylsilyloxy)ethyl)-2-((1-(4-chlorophenyl)cyclopentyl)methyl)-6-hydroxy-N-(1,1,1-trifluoropropan-2-yl)pyrimidine-4-carboxamide (42) (oil, 138 mg, 199 μmol, 58.3% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09045486B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-afe21fbb8ac64f81b1509f78d6360f15
Quellennotizuspto-grants-2015_06