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HRID 1397135Erstellt: 26. Oktober 2026

Potassium Carbonate → 4'-(Cyclopropylmethyl)-2-(methylsulfanyl)-4,5'-bipyrimidine

https://huagongshe.com/reaction/1397135

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktFormamidine acetateHCID 160693—
Edukt(3Z)-1-Cyclopropyl-4-(dimethylamino)-3-[2-(methylsulfanyl)pyrimidin-4-yl]but-3-en-2-oneHCID 67983763—
LösungsmittelDimethylformamideHCID 6228—
Produkt4'-(Cyclopropylmethyl)-2-(methylsulfanyl)-4,5'-bipyrimidineHCID 6798376133,6%

Reaktionsschritte

A solution of (3Z)-1-cyclopropyl-4-(dimethylamino)-3-[2-(methylsulfanyl)pyrimidin-4-yl]but-3-en-2-one (3) (200 mg, 0.721 mmol), formamidine acetate (75 mg, 0.721 mmol), and K2CO3 (299 mg, 2.163 mmol) in DMF (6 mL) was stirred at 120° C. for 30 minutes, followed by stifling at rt for 18 hours. The reaction was partitioned between water and EtOAc. The organic layer was separated, and the aqueous layer was back-extracted. The organic extracts were combined, washed with brine, dried over sodium sulfate, then concentrated in vacuo. The crude product was purified by Biotage™ silica gel chromatography [10 g SNAP column, 30% EtOAc/heptane to 100% EtOAc] to obtain the desired product as a white solid (62.5 mg, 29.4% yield). The desired product contained a small amount of an unknown by-product and was carried on to the next step without further purification. MS (ES+): m/z=259.3 (100) [MH+2]. HPLC: tR=1.77 minutes over 3 minutes. Purity: 87.5% [HPLC (LC/MS) at 220 nm].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08901147B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-6a85f3ae292b40f993c5cd848596471f
Quellennotizuspto-grants-2014_12