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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358431Generated: November 3, 2026

1-Tert-butyl-4-isocyanatobenzene → N-{4-[3-(4-tert-Butylphenyl)ureidomethyl]-2-fluoro-6-vinylphenyl}methanesulfonamide

https://huagongshe.com/reaction/2358431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Tert-butyl-4-isocyanatobenzeneHCID 2735695—
ReactantHCID 57665528HCID 57665528—
SolventDichloromethaneHCID 6344—
ProductN-{4-[3-(4-tert-Butylphenyl)ureidomethyl]-2-fluoro-6-vinylphenyl}methanesulfonamideHCID 1185300156.6%

Reaction Steps

N-(4-Aminomethyl-2-fluoro-6-vinylphenyl)methanesulfonamide (37.8 mg, 0.11 mmol), 1-tert-butyl-4-isocyanatobenzene (1.2 eq, 0.13 mmol, 22.49 μl), and TEA (3 eq, 0.33 mmol, 45.99 μl) were added in methylene chloride. The reaction mixture was stirred for 12 hrs. The reaction mixture was extracted with methylene chloride. A combined organic layer was washed with H2O and brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified with column chromatography (n-Hx:EA=1:1) to yield title compound (26.1 mg, 55%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763657B2
Source datasetuspto-grants-2010_07
ORD IDord-508ca1d30fe643ab963c69de6623e90a
Source noteuspto-grants-2010_07