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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423078Generated: October 26, 2026

4-Toluenesulfonyl chloride → 5-Bromo-4-Chloro-7-Tosyl-7H-Pyrrolo[2,3-D]Pyrimidine

https://huagongshe.com/reaction/423078

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
Reactant5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5380710—
SolventAcetoneHCID 180—
Product5-Bromo-4-Chloro-7-Tosyl-7H-Pyrrolo[2,3-D]PyrimidineHCID 5775028299%

Reaction Steps

5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine (Intermediate 50) (2 g, 8.60 mmol) and p-toluenesulfonyl chloride (1.640 g, 8.60 mmol) was taken up in acetone (12 mL) and stirred under nitrogen and cooled to between −5° C. and 5° C. To this solution was added 2.0M NaOH solution (5.50 mL, 10.99 mmol) while maintaining the internal temperature at less than 5° C. The reaction was allowed to warm to room temperature and stirred for 1 hour. The white solid was filtered off and washed well with acetone to afford 5-bromo-4-chloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine (3.28 g, 99%) as a pale cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101623B2
Source datasetuspto-grants-2012_01
ORD IDord-45c9b267ca0e4defbb32d5116da05eb0
Source noteuspto-grants-2012_01