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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805869Generated: November 2, 2026

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

https://huagongshe.com/reaction/1805869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-benzyl-2,4-dichloro-5H-pyrrolo[3,2-d]pyrimidineHCID 14727765—
Solvent1,2-DichlorobenzeneHCID 7239—
Product2,4-Dichloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5375053—

Reaction Conditions

Temperature160 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354532B2
Source datasetuspto-grants-2013_01
ORD IDord-dca03797087a4c1b9900f3e2da59db8a
Source noteuspto-grants-2013_01