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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686875Generated: November 2, 2026

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

https://huagongshe.com/reaction/1686875

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 numberUS08148503B2
Source datasetuspto-grants-2012_04
ORD IDord-129717a43df54a0aaf3c7786a08564f0
Source noteuspto-grants-2012_04