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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358392Generated: November 1, 2026

Di-tert-butyl dicarbonate → N-{4-[3-(4-tert-Butylbenzyl)ureidomethyl]-2-trifluoromethyl-6-vinylphenyl}methanesulfonamide

https://huagongshe.com/reaction/2358392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant4-tert-ButylbenzylamineHCID 2735655—
Reactant1-Tert-butyl-4-(isocyanatomethyl)benzeneHCID 22042227—
ReactantN-(4-Aminomethyl-2-trifluoromethyl-6-vinylphenyl)methanesulfonamideHCID 68453783—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-{4-[3-(4-tert-Butylbenzyl)ureidomethyl]-2-trifluoromethyl-6-vinylphenyl}methanesulfonamideHCID 5766552936.88%

Reaction Steps

4-tert-Butyl-benzylamine (1.5 eq, 15.20 μl, 0.09 mmol), BOC2O (1.5 eq, 0.09 mmol, 20.70 μl), and DMAP (0.2 eq, 0.01 mmol, 1.34 mg) were added to methylene chloride. The reaction mixture was stirred for 5 hr. After confirming the synthesis of the 1-tert-butyl-4-isocyanatomethylbenzene with TLC, N-(4-Aminomethyl-2-trifluoromethyl-6-vinylphenyl)methanesulfonamide (1 eq, 0.06 mmol, 20.5 mg) and TEA (2 eq, 0.12 mmol, 16.72 μl) were added into the reaction mixture. The reaction mixture was stirred for 12 hr and purified with similar procedure to step 7 of example 8 to gave title compound (10.7 mg 36.88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763657B2
Source datasetuspto-grants-2010_07
ORD IDord-8c561c387b4e4d29a01cdb79b87c7353
Source noteuspto-grants-2010_07