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HRID 1516849Erstellt: 25. Oktober 2026

Chloroform → 2,4-Dichloro-5H-pyrrolo[3,2-d]pyrimidine

https://huagongshe.com/reaction/1516849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
EduktAluminum(III) ChlorideHCID 6451240—
Edukt5-benzyl-2,4-dichloro-5H-pyrrolo[3,2-d]pyrimidineHCID 14727765—
Lösungsmittel1,2-DichlorobenzeneHCID 7239—
Produkt2,4-Dichloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5375053—

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

To a suspension of 5-benzyl-2,4-dichloro-5H-pyrrolo[3,2-d]pyrimidine (177 mg, 0.64 mmol) in 1,2-dichlorobenzene (20 mL) was added AlCl3 (852 mg, 6.4 mmol). The reaction mixture was heated at 160° C. for 1.5 h, during which the reaction mixture became dark and homogeneous. Upon completion of the reaction, the reaction mixture was cooled, added CHCl3 and washed with NH4Cl. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. Added Hexanes and filtered off the product as purple solids (100 mg, 80%) and used for the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08227601B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-d3142205af50431d87bbc2c7b566f4c4
Quellennotizuspto-grants-2012_07