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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1966825Erstellt: 26. Oktober 2026

Chloroform → ethyl 5-(bromomethyl)-3-[4-(cyclohexylamino)-1-ethyl-1H-pyrazolo[3,4-b]pyridin-5-yl]-4,5-dihydroisoxazole-5-carboxylate

https://huagongshe.com/reaction/1966825

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
Edukt2-(Bromomethyl)acrylic acid ethyl esterHCID 310620—
EduktSodium HypochloriteHCID 23665760—
Edukt4-cyclohexylamino-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde oximeHCID 86647599—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produktethyl 5-(bromomethyl)-3-[4-(cyclohexylamino)-1-ethyl-1H-pyrazolo[3,4-b]pyridin-5-yl]-4,5-dihydroisoxazole-5-carboxylateHCID 6673263566%

Reaktionsschritte

4-(Cyclohexylamino)-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde oxime (200 mg, 0.0006 mole) (example 8) was taken in dichloromethane: chloroform mixture (10 ml: 5 ml). Ethyl 2-(bromomethyl)acrylate (0.2 ml, 0.00103 mole) was added. Sodium hypochlorite (2.5 ml) was added drop wise. The reaction mixture was stirred overnight. Water was added, the mixture was extracted with chloroform, washed with brine, dried over anhydrous sodium sulphate and concentrated in vacuo. The crude compound obtained was purified by column chromatography.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08420666B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-303416e2845e487a912e17b70c68038f
Quellennotizuspto-grants-2013_04