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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423350Generated: November 3, 2026

N-{4-[3-(4-t-butyl-benzyl)-ureidomethyl]-2-fluoro-6-vinyl-phenyl}methanesulfonamide → N-{4-[3-(4-t-butylbenzyl)ureidomethyl]-2-ethyl-6-fluorophenyl}methanesulfonamide

https://huagongshe.com/reaction/2423350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-{4-[3-(4-t-butyl-benzyl)-ureidomethyl]-2-fluoro-6-vinyl-phenyl}methanesulfonamideHCID 11852379—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-{4-[3-(4-t-butylbenzyl)ureidomethyl]-2-ethyl-6-fluorophenyl}methanesulfonamideHCID 11851687100%

Reaction Steps

N-{4-[3-(4-t-butyl-benzyl)-ureidomethyl]-2-fluoro-6-vinyl-phenyl}methanesulfonamide (15.6 mg, 0.04 mmol) was dissolved in methanol. To the solution was added Pd/C (10 wt. %) and air in the flask was displaced with hydrogen gas. The reaction solution was stirred for 1 hour. After confirming the completion of the reaction with TLC, Pd/C was filtered off through celite. The methanol was removed under reduced pressure and column-chromatographed (n-hexane/ethyl acetate ˜1/1) to yield a white solid (15.8 mg, 100.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960584B2
Source datasetuspto-grants-2011_06
ORD IDord-6494be783fa84cf58ec68f3733ba02f7
Source noteuspto-grants-2011_06