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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31715Erstellt: 24. Oktober 2026

Dimethyl Sulfoxide → 4-((2,2-dimethyl-1,3-dioxan-5-yl)methoxy)-3-ethyl-N,N-diisopropylpyridine-2-carboxamide

https://huagongshe.com/de/reaction/31715

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktSodium hydrideHCID 24758—
Edukt(2,2-Dimethyl-1,3-dioxan-5-yl)methanolHCID 3584869—
EduktHCID 59792465HCID 59792465—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-((2,2-dimethyl-1,3-dioxan-5-yl)methoxy)-3-ethyl-N,N-diisopropylpyridine-2-carboxamideHCID 5979255936,9%

Reaktionsschritte

To a dimethylsulfoxide (20 ml) solution of the 4-chloro-3-ethyl-N,N-diisopropylpyridine-2-carboxamide (1 g, 3.72 mmol) obtained in the step (92b) above, oily sodium hydride, in oil (195 mg, 4.46 mmol as the content was regarded as 55%) was added at room temperature. To the mixture, the (2,2-dimethyl-1,3-dioxan-5-yl)methanol (598 mg, 4.09 mmol) obtained in Example (11a) was added and the mixture was stirred at room temperature for 16.5 hours. Ethyl acetate was added to the reaction mixture. The mixture was washed twice with a saturate saline solution. The organic layer was dried over anhydrous magnesium sulfate, filtrated, and concentrated. The residue was washed with diethyl ether to obtain the title compound (520 mg, yield: 36.9%) as a light yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425634B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-faf7a348652c48d4ac613a0eb85291d2
Quellennotizuspto-grants-2008_09