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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059574Generated: October 31, 2026

N-Iodosuccinimide → HCID 178478409, compound

https://huagongshe.com/reaction/2059574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
ReactantAluminumHCID 5359268—
SolventDimethylformamideHCID 6228—
ProductHCID 178478409HCID 178478409—

Reaction Steps

To a 250 ml round-bottomed flask, protected from light with aluminum foil, are added 4-chloro-7H-pyrrolo[2,3-d]pyrimidine 1 (2.15 g, 14.0 mmol) and N-iodosuccinimide (3.37 g, 14.98 mmol) dissolved in anhydrous DMF. The reaction mixture is stirred at room temperature under nitrogen for 16 hrs. The solvent is removed in vacuo, and the residue is dissolved in methylene chloride (250 ml). The reaction mixture is washed with brine (50 ml), and the organic layer is separated, dried over Na2SO4, and concentrated in vacuo. The crude residue is purified by flash-chromatography on silica gel and eluted with 60% EtOAc in cyclohexane. Fractions containing the desired product (TLC) are pooled and evaporated to afford 4-chloro-5-iodo-pyrrolo[2,3-d]pyrimidine as a pale-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278282B2
Source datasetuspto-grants-2012_10
ORD IDord-60b9a4d18aac4daf82bf67d2b6f5e56c
Source noteuspto-grants-2012_10