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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948197Generated: October 26, 2026

Sodium Iodide → 1-(4-chloro-3-fluorobenzyl)-5-(benzo[d]thiazol-2-yl)pyridin-2(1H)-one

https://huagongshe.com/reaction/1948197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant4-(Bromomethyl)-1-chloro-2-fluorobenzeneHCID 2783136—
Reactant2-(6-Methoxypyridin-3-yl)benzo[d]thiazoleHCID 69345566—
SolventAcetonitrileHCID 6342—
Product1-(4-chloro-3-fluorobenzyl)-5-(benzo[d]thiazol-2-yl)pyridin-2(1H)-oneHCID 5896691358%

Reaction Conditions

Temperature90 °C

Reaction Steps

According to Scheme 4, Step 1: A mixture of 2-(6-methoxypyridin-3-yl)benzo[d]thiazole (1 eq, 0.25 mmol, 60 mg), NaI (5 eq, 1.20 mmol, 0.19 g) and 4-chloro-3-fluorobenzylbromide (5 eq, 1.20 mmol, 0.28 g) in acetonitrile (10 mL) was stirred for 14 hours at 90° C. The crude residue was partitioned between CH2Cl2 and water. The aqueous layer was extracted with CH2Cl2. The combined organic layers were dried over MgSO4, filtered and evaporated. The crude product was purified by silica gel chromatography (AIT Flashsmart prepacked column 25 g SiO2) using CH2Cl2/AcOEt 95/5 as eluent to afford 1-(4-chloro-3-fluorobenzyl)-5-(benzo[d]thiazol-2-yl)pyridin-2(1H)-one (0.14 mmol, 0.05 g, 58%) as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399493B2
Source datasetuspto-grants-2013_03
ORD IDord-76ff8b448aea4196abc137e7c73da643
Source noteuspto-grants-2013_03