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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1051768Erstellt: 26. Oktober 2026

Thionyl Chloride → 4-Chloro-7H-pyrrolo(2,3-d)pyrimidine-5-carbonitrile

https://huagongshe.com/reaction/1051768

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThionyl ChlorideHCID 24386—
EduktCID 136342890HCID 136342890—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Chloro-7H-pyrrolo(2,3-d)pyrimidine-5-carbonitrileHCID 22484542—

Reaktionsschritte

To a suspension of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehyde oxime (G-3) (865 mg, 4.40 mmol, 1.0 eq) in DCM (20 mL), thionyl chloride (3.1 mL, 43.7 mmol, 10.0 eq) is added and the resulting mixture is stirred at RT overnight. The reaction mixture is concentrated in vacuo. The residue is suspended in water (60 mL) and saturated aqueous NaHCO3 is added to adjust the pH to 4. The solid is collected by filtration, rinsed with water and followed by ethyl acetate to afford the first batch of product. The filtrate is extracted with ethyl acetate (3×50 mL). The combined organic layers are washed with brine, dried over Na2SO4 and filtered. The filtrate is concentrated in vacuo and the residue is combined with the above-obtained solid. The product is re-crystallized in ethyl acetate/hexanes (v/v=1/1) and dried in vacuo to afford the product, 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile (G-4).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09388183B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-3bf176cabbf944dead63803e35249963
Quellennotizuspto-grants-2016_07