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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403266Generated: October 27, 2026

N-Iodosuccinimide → 4-cyclopentyl-5-iodo-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/1403266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant4-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidineHCID 11636952—
SolventDichloromethaneHCID 6344—
Product4-cyclopentyl-5-iodo-7H-pyrrolo[2,3-d]pyrimidineHCID 57963205371.2%

Reaction Steps

4-Cyclopentyl-7H-pyrrolo[2,3-d]pyrimidine (48, 0.099 g, 0.53 mmol) was dissolved in 3.4 mL of dichloromethane under an atmosphere of nitrogen and N-iodosuccinimide (0.131 g, 0.582 mmol) was added. The mixture was stirred overnight, then quenched with aqueous sodium thiosulfate. The aqueous layer was separated and washed with ethyl acetate. The organic layers were combined and washed with water, brine, dried over sodium sulfate and filtered. The filtrate was concentrated under vacuum to provide the desired compound (49, 0.616 g), used in the next step without further purification. MS (ESI) [M+H+]+=313.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912204B2
Source datasetuspto-grants-2014_12
ORD IDord-cbfab2bb2be5493185c9a79db5d4cc4e
Source noteuspto-grants-2014_12