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Merck

Synthesis of trisubstituted ureas by a multistep sequence utilizing recyclable magnetic reagents and scavengers.

Chemistry (Weinheim an der Bergstrasse, Germany) (2013-06-19)
Quirin M Kainz, Martin Zeltner, Michael Rossier, Wendelin J Stark, Oliver Reiser
RESUMEN

Unprecedented magnetic borohydride exchange (mBER), magnetic Wang aldehyde (mWang) and magnetic amine resins were prepared from highly magnetic polymer-coated cobalt or iron nanoparticles. Microwave irradiation was used to obtain excellent degrees of functionalization (>95 %) and loadings (up to 3.0 mmol  g(-1)) in short reaction times of 15 min or less. A small library of ureas and thioureas was synthesized by the exclusive application of these magnetic resins. As a first step, a reductive amination of aromatic and aliphatic aldehydes was carried out with mBER. The excess of primary amine needed to complete the reaction was subsequently scavenged selectively by mWang. Simple magnetic decantation from the resins resulted in secondary amines in good to excellent yields and purities. The used magnetic resins were efficiently regenerated and reused for the next run. In a second step, the secondary amines were converted to trisubstituted (thio)ureas in excellent yields and purities by stirring with an excess of iso(thio)cyanate, which was scavenged by addition of the magnetic amine resin after completion of the reaction. The whole reaction sequence is carried out without any purification apart from magnetic decantation; moreover, conventional magnetic stirring can be used as opposed to the vortexing required for polystyrene resins.

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Sigma-Aldrich
TurboBeads Silica, extent of labeling: SiO2 loading (Silica coating))
Sigma-Aldrich
TurboBeads Complexon, extent of labeling: ≥0.1 mmol/g loading (-Ph-CH2-N(CH2-COOH)2)