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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728396Generated: October 30, 2026

Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea

https://huagongshe.com/reaction/1728396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
SolventTetrahydrofuranHCID 8028—
ProductN,N'-DicyclohexylureaHCID 4277—

Reaction Steps

A mixture of 13 (52 mg, 0.058 mmol), HOBT (10 mg, 0.065 mmol) and DCC (16mg, 0.079 mmol) in THF (2 ml) was stirred for 1 hour at room temperature and filtered to remove resulting dicyclohexyl urea. The filtrate was concentrated and the residue was dissolved in 1 ml of 50% aqueous dioxane. To the mixture was added a solution of D-3,4-dihydroxyphenylalanine (D-DOPA) (24 mg, 0.12 mmol) and triethylamine (20 μl, 0.14 mmol) in 1 ml of 50% aqueous dioxane. The mixture was stirred for 1 day at room temperature and then dioxane was removed under reduced pressure. To the residue was added 50 ml of H2O and the mixture was acidified with 1N HC1 to pH 2. The precipitate formed was collected by filtration and chromatographed on a column of C-18 silica gel (Bondpak C18, 20 i.d. ×200 mm). The column was eluted with 30-40% acetonitrile-1/1000N HC1 and the desired fraction was concentrated and lyophilized to give 4'N-CBZ protected title compound (23 mg, yield 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05326867
Source datasetuspto-grants-1994_07
ORD IDord-3558d22d2ddf4004aef55e8abbd42bc3
Source noteuspto-grants-1994_07