Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246359Generated: October 29, 2026

Iodine → HCID 178478165, compound

https://huagongshe.com/reaction/246359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium HydroxideHCID 14797—
Reactant5-(3-chlorophenoxy)-1H-indazoleHCID 71280518—
SolventDimethylformamideHCID 6228—
ProductHCID 178478165HCID 17847816584.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 5-(3-chlorophenoxy)-1H-indazole (152 mg, 621 μmol) in DMF (2.36 mL) at 25° C. was added potassium hydroxide (105 mg, 1.86 mmol) and iodine (237 mg, 932 μmol). The reaction mixture was stirred at 25° C. for 75 min then quenched with 10% Na2S2O3 and diluted with water. The mixture was extracted with EtOAc (3×), then the combined organics were washed with water and brine (2×), dried over MgSO4 and concentrated to afford a pale yellow oil which was purified by chromatography (silica, 115 g, 50 μm from Analogix, 0 to 30% EtOAc in hexanes, 15 min) to give 5-(3-chlorophenoxy)-3-iodo-1H-indazole (194 mg, 524 μmol, 84%) as an off-white solid. MS (M+H)+=370.8; 1H NMR (CDCl3) δ: 7.73 (d, J=8.7 Hz, 1H), 7.28 (d, J=5.3 Hz, 1H), 7.22-7.25 (m, 1H), 7.17 (d, J=1.9 Hz, 1H), 7.08 (dt, J=7.9, 0.9 Hz, 1H), 6.98 (t, J=2.3 Hz, 1H), 6.89 (dd, J=8.3, 2.3 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-8b077765b4af45009e9590cd8d3ae54b
Source noteuspto-grants-2014_02