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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 219709Erstellt: 24. Oktober 2026

Sodium Iodide → (S)-Acetic acid 3-[4-(2-tert-butyl-6-cyclobutyl-pyrimidin-4-yl)-piperazin-1-yl]-2-methyl-propyl ester

https://huagongshe.com/de/reaction/219709

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktTriethylamineHCID 8471—
Edukt(R)-(-)-1-acetoxy-3-bromo-2-methyl-propaneHCID 10420167—
Edukt2-tert-Butyl-4-cyclobutyl-6-(piperazin-1-yl)pyrimidineHCID 66673390—
LösungsmittelDimethylformamideHCID 6228—
Produkt(S)-Acetic acid 3-[4-(2-tert-butyl-6-cyclobutyl-pyrimidin-4-yl)-piperazin-1-yl]-2-methyl-propyl esterHCID 131729779102,9%

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

3.87 g of 2-tert-butyl-4-cyclobutyl-6-piperazin-1-yl-pyrimidine (14.1 mmol) were stirred in 30 ml of dimethylformamide at room temperature. 3.18 g of triethylamine (63.1 mmol), 0.235 g of sodium iodide (1.57 mmol), 2.96 g of (R)-(−)-1-acetoxy-3-bromo-2-methyl-propane (15.2 mmol) were added and the reaction mixture was stirred for 5 h at 95° C. The dimethylformamide was evaporated under reduced pressure. The residue was partitioned between 100 ml of dichloromethane and 100 ml of water. The organic layer was separated, dried over magnesium sulfate and evaporated under reduced pressure to give a brownish oil (5.64 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202868B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-8ad93d4589f643a19d73bbb7382181e8
Quellennotizuspto-grants-2012_06