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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295552Generated: October 30, 2026

N-Iodosuccinimide → 6-Chloro-7-iodo-7-deazapurine

https://huagongshe.com/reaction/1295552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
SolventDimethylformamideHCID 6228—
Product6-Chloro-7-iodo-7-deazapurineHCID 1480928174.6%

Reaction Steps

4-Chloro-7H-pyrrolo[2,3-d]pyrimidine 10.75 g (70 mmol) and N-iodosuccinimide (16.8 g, 75 mmol) were dissolved in 400 mL of dry DMF and left at ambient temperature in the darkness over night. The solvent was evaporated. The yiellow residue was suspended in hot 10% solution of Na2SO3, filtered, washed twice with hot water and crystallized from ethanol to yield 14.6 g (74.6%) of the title compound as off-white crystals. The mother liquid was evaporated up to ⅓ volume and crystallized again from ethanol to give 2.47 g (12.3%) of the title product. The total yield is close to 100%;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244713B2
Source datasetuspto-grants-2007_07
ORD IDord-41532b9d1456434baae63c96128b6f3e
Source noteuspto-grants-2007_07