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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854384Generated: October 31, 2026

4-Toluenesulfonyl chloride → 4-Methoxy-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/854384

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
Reactant4-Methoxy-7h-pyrrolo[2,3-d]pyrimidineHCID 248792—
CatalystBis(tetrabutylammonium) sulphateHCID 11433187—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-Methoxy-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidineHCID 6943182991.4%

Reaction Steps

A solution of 4-methoxy-7H-pyrrolo[2,3-d]pyrimidine [1.2 g, Reference Example 8] and para-toluene sulfonylchloride (1.77 g) in toluene (60 mL) was treated with a solution of sodium hydroxide (3.2 g) in water (30 mL), and tetrabutyl ammonium sulfate (27 mg). The solution was stirred vigorously at room temperature for 4 hours and partitioned between ethyl acetate and brine. The organic phase was separated, then dried over magnesium sulfate and then evaporated under reduced pressure. The residue was subjected to flash column chromatography on silica eluting with a gradient of ethyl acetate and cyclohexane (50:50 to 80:20, v/v) to give the title compound (2.23 g) as an amorphous solid. MS: 304 [MH]+. LCMS (Method B) RT=3.88 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259154B2
Source datasetuspto-grants-2007_08
ORD IDord-563eec4e7d6744de9f576d704c258940
Source noteuspto-grants-2007_08