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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948194Generated: October 26, 2026

5-Bromo-1-[(4-chlorophenyl)methyl]-1,2-dihydropyridin-2-one → HCID 11683170, compound

https://huagongshe.com/reaction/1948194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-1-[(4-chlorophenyl)methyl]-1,2-dihydropyridin-2-oneHCID 60372773—
ReactantHCID 69345138HCID 69345138—
ProductHCID 11683170HCID 1168317041%

Reaction Steps

According to Scheme 3 Method A: The title compound was prepared from 1-(4-chlorobenzyl)-5-bromopyridin-2(1H)-one (1 eq, 1.80 mmol, 0.55 g, Example 2 Step 1) and 4-methoxy-3-(methylsulfonamido)phenylboronic acid (1.1 eq, 2.00 mmol, 0.49 g) according to the procedure described for Example 1 Step 3. Reaction conditions: 4 hours at 80° C. The crude product was purified by flash chromatography over silica gel (AIT Flashsmart prepacked column 25 g SiO2) using CH2Cl2/AcOEt (90/10) then recrystallized from pentane/Et2O to afford N-(5-(1-(4-chlorobenzyl)-6-oxo-1,6-dihydropyridin-3-yl)-2-methoxyphenyl)methanesulphonamide (0.31 mmol, 0.32 g, 41%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399493B2
Source datasetuspto-grants-2013_03
ORD IDord-b11ce2e3bf444ba4a15c51cd548ecdf4
Source noteuspto-grants-2013_03