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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530031Generated: October 30, 2026

N-Iodosuccinimide → 2-Chloro-3-iodopyrazolo[1,5-A]pyridine

https://huagongshe.com/reaction/530031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant2-Chloropyrazolo[1,5-a]pyridineHCID 12284433—
SolventAcetonitrileHCID 6342—
Product2-Chloro-3-iodopyrazolo[1,5-A]pyridineHCID 71743340—

Reaction Steps

N-iodosuccinimide (1.06 g, 4.74 mmol) was added to a solution of 2-chloro-pyrazolo-[1,5-a]pyridine (27-2; 0.6 g, 3.95 mmol) in acetonitrile (18.0 mL). The resulting mixture was stirred at room temperature for 2 h and then concentrated under reduced pressure. The resulting residue was diluted with dichloromethane, washed with saturated aqueous sodium chloride solution, dried over magnesium sulphate, filtered and concentrated under reduced pressure. Purification by silica gel flash chromatography (5-10% ethyl acetate in hexanes) provided the title compound. 1H NMR (400 MHz, CDCl3) δ 8.36-8.34 (d, J=6.8 Hz, 1 H), 7.40-7.37 (d, J=8.8 Hz, 1 H), 7.26-7.23 (m, 1 H), 6.84-6.81 (m, 1 H). MS (M+1): 279.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09351973B2
Source datasetuspto-grants-2016_05
ORD IDord-026fe51dfcaf49f395c19ad0b857de4e
Source noteuspto-grants-2016_05