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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358379Generated: November 2, 2026

Di-tert-butyl dicarbonate → HCID 11852483, compound

https://huagongshe.com/reaction/2358379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant4-tert-ButylbenzylamineHCID 2735655—
Reactant1-Tert-butyl-4-(isocyanatomethyl)benzeneHCID 22042227—
ReactantHCID 68453767HCID 68453767—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 11852483HCID 1185248323.9%

Reaction Steps

4-tert-Butyl-benzylamine (1.5 eq, 71.91 μl, 0.44 mmol) was added in CH2Cl2 and then BOC2O (1.5 eq, 0.44 mmol, 101.19 μl) and DMAP (0.2 eq, 0.06 mmol, 7.08 mg) were slowly added. After confirming the synthesis of the 1-tert-Butyl-4-isocyanatomethyl-benzene, N-(4-Aminomethyl-2-methyl-6-vinyl-phenyl)-methanesulfonamide (1 eq, 0.29 mmol, 70.5 mg) and TEA (2 eq, 0.58 mmol, 80.84 μl) were added into the reaction mixture. The reaction mixture was stirred for 12 hr. The reaction mixture was purified according to step 9 of example 7 to obtain N-{4-[3-(4-tert-Butyl-benzyl)ureidomethyl]-2-methyl-6-vinylphenyl}methanesulfonamide (29.75 mg, 23.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763657B2
Source datasetuspto-grants-2010_07
ORD IDord-1c4618e98f514161bad89e349c87fd56
Source noteuspto-grants-2010_07