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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611531Generated: October 30, 2026

Toluene → 4-Chloro-7-isopropyl-5-(4-nitrophenyl)pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/611531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Nitrophenylboronic acidHCID 2773552—
Reactant4-Chloro-5-iodo-7-(propan-2-yl)-7H-pyrrolo[2,3-d]pyrimidineHCID 19597426—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-Chloro-7-isopropyl-5-(4-nitrophenyl)pyrrolo[2,3-d]pyrimidineHCID 19597481—

Reaction Conditions

Temperature105 °C

Reaction Steps

A mixture of 4-chloro-5-iodo-7-isopropylpyrrolo[2,3-d]pyrimidine (0.57 g), 4-nitrophenylboronic acid (0.30 g), bis(triphenylphosphine)palladium (II) chloride (0.126 g), toluene (15 ml), ethanol (2 ml), water (4 ml) and sodium bicarbonate (0.45 g) was heated under nitrogen at 105° C. for 8 hours. The mixture was cooled to ambient temperature and then partitioned between brine (50 ml) and ethyl acetate (50 ml). The aqueous layer was further extracted with ethyl acetate and the combined ethyl acetate extracts were washed with water, dried, filtered and evaporated to leave a solid which was purified by flash column chromatography on silica using cyclohexane with increasing amounts of ethyl acetate as the mobile phase to give 4-chloro-7-isopropyl-5-(4-nitrophenyl)pyrrolo[2,3-d]pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06001839
Source datasetuspto-grants-1999_12
ORD IDord-e4bd162e3c0b4c23a0239173e397c33f
Source noteuspto-grants-1999_12