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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333480Generated: October 29, 2026

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

https://huagongshe.com/reaction/333480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
SolventDichloromethaneHCID 6344—
Product6-Chloro-7-iodo-7-deazapurineHCID 14809281—

Reaction Steps

Compound dA.23 was synthesized according to the procedure described by Ju et al. (2006, which is incorporated herein by reference). To a suspension of 6-chloro-7-deazapurine (1.00 g, 6.51 mmol) in anhydrous CH2Cl2 (55 mL) was added N-iodosuccinimide (1.70 g, 7.56 mmol). The reaction was protected from light while stirring at room temperature for two hours. The reaction was then concentrated down in vacuo. The material was re-crystallized from hot methanol to yield 6-chloro-7-iodo-7-deazapurine dA.23 (0.94 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877905B2
Source datasetuspto-grants-2014_11
ORD IDord-b749bf6e24074e40aa4bebb2d3b49429
Source noteuspto-grants-2014_11