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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252708Generated: November 2, 2026

Methanol → 5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/2252708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-bromobutanimideHCID 67184—
Reactant7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
SolventDimethylformamideHCID 6228—
Product5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5380710—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (4-1) (1.53 g, 10.0 mmol) in DMF (20 mL) was added N-bromosuccinimide (1.78 g, 10.0 mmol) in DMF (10 mL) dropwise at 0° C. The reaction mixture was stirred at 0° C. for 30 min and then at room temperature for 1 h. Methanol (25 mL) was added, and the reaction mixture was stirred for an additional 1 h. The solvent was evaporated and the residue was crystallized from methanol to give the title compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323453B2
Source datasetuspto-grants-2008_01
ORD IDord-ee0bb1355c2d4cecbe8f82f074459bf3
Source noteuspto-grants-2008_01