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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692836Generated: November 2, 2026

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

https://huagongshe.com/reaction/1692836

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 numberUS08158636B2
Source datasetuspto-grants-2012_04
ORD IDord-42307225dbbc406aafeeabe8ed3d0a3e
Source noteuspto-grants-2012_04