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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064691Generated: October 25, 2026

Sodium Iodide → 2-Iodo-4-[5-(4-morpholinylcarbonyl)-2-pyridinyl]phenol

https://huagongshe.com/reaction/1064691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium HydroxideHCID 14798—
Reactant4-[5-(4-Morpholinylcarbonyl)-1,6-dihydro-2-pyridinyl]phenolHCID 22274692—
ReactantSodium HypochloriteHCID 23665760—
SolventMethanolHCID 887—
Product2-Iodo-4-[5-(4-morpholinylcarbonyl)-2-pyridinyl]phenolHCID 13572107161.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of Example 44B (4.25 g, 15.0 mmol) sodium iodide (2.36 g, 15.7 mmol) and sodium hydroxide (0.63 g, 15.7 mmol) was stirred in methanol (90 mL) with heating until a clear solution was obtained. The solution was then cooled to 0° C. and to this was slowly added sodium hypochlorite (22 mL of 5.25%, 1.15 g, 15.5 mmol) (Clorox™) over 45 minutes. While maintaining 0° C., two sequential additions of NaI (0.3 g, 1.5 mmol) and Clorox (2.2 mL, 0.12 g, 1.5 mmol) were made both 2 hours and 4 hours later. The mixture was stirred for 12 hours at ambient temperature, quenched by the sequential addition of aqueous sodium thiosulfate (10 mL), water (800 mL) and sufficient aqueous sodium dihydrogen phosphate (NaH2PO4) to adjust the pH to 7. The mixture was extracted with dichloromethane, and the combined extracts dried (Na2SO4), filtered and concentrated under reduced pressure to give a tan foam. The product was crystallized from ethanol to give the titled compounds as a tan solid (3.78 g, 61%). MS (DCI) m/z 411 (M+H)+;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969730B2
Source datasetuspto-grants-2005_11
ORD IDord-e4cab47974fd4d1081074a432dba70f0
Source noteuspto-grants-2005_11