Alasdair A.
MacDonald*, William S. Newcomb and John
A. Porco, Jr.
Argonaut
Technologies, San Carlos, CA, USA
E-mails: (Alasdair A. MacDonald) amacdonald@jason.argotech.com, (William S. newcomb) nuke@jason.argotech.com, (John A. Porco, Jr.) jporco@jason.argotech.com, (Mark Scialdone) scialdma@esvax.dnet.dupont.com, (Steven W. Shuey) shueysw@esvax.dnet.dupont.com
Received: 7 July 1997 / Uploaded: 11 July 1997
Abstract: Phosgenated p-nitrophenyl(polystyrene)ketoxime
(Phoxime) resin (1) has been previously utilized as a
latent isocyanate equivalent. The Nautilus 2400 automated
organic synthesizer was used to determine the optimal temperature for
thermolysis of the polymer-bound oxime-carbamate derived from Phoxime
resin and subsequent amine addition to give a urea in solution.
Isocyanates are useful building blocks for combinatorial synthesis and have been utilized for the preparation of ureas,1-3 carbamates,4-6 sulfonylureas7-9 and heterocycles such as hydantoins10,11 and quinazoline-2,4-diones.12-14 Polymer-bound oxime carbamates derived from the addition of isocyanates to p-nitrophenyl(polystyrene) ketoxime or Phoxime resin15,16 have been shown to serve as latent isocyanates upon thermolysis.17 Phosgenation of the oxime resin to afford its chloroformate and subsequent addition of a primary amine, results in the formation of an oxime-carbamate.18 Urea formation then occurs in solution upon thermolysis19 of the polymer-bound oxime-carbamate in the presence of an amine.
The suitability of the Nautilus 2400 automated synthesizer for development and optimization of organic synthesis has been well established. Typical optimization studies include: reaction temperature, reaction time, reagents, solvents and stoichiometry. To examine the dependence of isolated urea yield and purity on the thermolysis temperature for the polymer-bound oxime-carbamate derived from Phoxime resin, the Nautilus 2400 was employed to independently control reactor temperature from vessel-to-vessel. As a case study, we chose to look at the synthesis of cyclohexyl-4-biphenyl urea (2).

Phoxime resin 1 (200 mg, 0.15 mmol) was added to eight, 8 mL reaction vessels (RV's) on the Nautilus 2400. Three molar equivalents of 4-biphenylamine in dichloromethane (DCM) was added to each reaction vessel and agitated (25 °C, 2 h) to afford a resin-bound oxime carbamate intermediate, which was washed with DCM followed by methanol (Scheme 1). Heating of the oxime-derived carbamate resin in toluene at eight independent temperatures from 50 sC to 120 sC at 10 sC increments for 10h in the presence of four equivalents of cyclohexylamine formed cyclohexyl-4-biphenyl urea 2 in solution.
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Urea products 2 were evaporated to dryness and analyzed by 1H NMR,mass spectroscopy and HPLC.18 High purity (HPLC area %) and chemical yields were observed. For this particular case, optimum thermolytic cleavage conditions appear to be above 80 °C as shown in Table 1. Additionally, inspection of the IR spectra of the recovered oxime resin from the higher temperatures indicated complete cleavage of the polymer-supported oxime carbamate (CO stretch: 1750 cm-1). |
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Comments
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