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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186828Generated: November 4, 2026

Chlorosuccinimide → 3-Chloro-1-(4-fluorophenyl)-4-iodo-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/1186828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant1-(4-Fluorophenyl)-4-iodo-1H-pyrazolo[3,4-B]pyridineHCID 66668437—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-Chloro-1-(4-fluorophenyl)-4-iodo-1H-pyrazolo[3,4-b]pyridineHCID 68058280—

Reaction Steps

To a solution of Intermediate 2A (33.9 mg, 0.1 mmol) in DMF (Volume: 1 mL) under argon at room temp was added N-chlorosuccinimide (107 mg, 0.800 mmol). The reaction mixture was allowed to stir overnight. The reaction mixture was diluted with ethyl acetate and washed (2×15 mL) with 10% LiCl, once with brine, dried over Na2SO4, filtered and concentrated. The crude product was dissolved in a small amount of dichloromethane and charged to a 4 g silica gel cartridge which was eluted with a 20 min gradient from 0% to 100% of ethyl acetate in dichloromethane. The resulting brown solid (23 mg, 61.6%) was determined to be the desired material by 1HNMR and LCMS. MS (ES): m/z=274.0 [M+H]+. 1H NMR (400 MHz, CCl3D) δ ppm 8.58-8.60 (1 H, m), 8.24 (1 H, s), 8.14-8.20 (2 H, m), 7.18-7.26 (2 H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673922B2
Source datasetuspto-grants-2014_03
ORD IDord-6e79f23b4f21406ab1950b49188eb6f4
Source noteuspto-grants-2014_03