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haozi029228

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[½»Á÷] 30½ð±ÒÇóÓ¢Ò뺺һ¶ÎÎÄ×Ö

As mentioned, it was of interest to further transform
precipitated products (after redissolution in a suitable
solvent) using polymer-supported reagent and scavenger
techniques. This approach utilizes a tactical combination
of classical solution-phase synthesis followed
by ¡°chemically driven¡± synthesis and purification. As
a first example of precipitation followed by a polymerassisted
reaction, we prepared 2-aminothiazole hydrobromide
monohydrates on the Quest 210 synthesizer
(7-mmol scale), redissolved the solid products in solvent
(e.g., methanol or dimethylformamide), and freebased
the compounds in the same reaction vessel using
polymer-supported bases (Scheme 2). Two polymeric
bases were found to be effective: MP-Carbonate (Macroporous
triethylammonium methyl polystyrene carbonate
resin), a resin-bound equivalent of potassium
carbonate (K2CO3)10¨C12 and PS-DIEA (N,N-(Diisopropyl)
aminomethyl- polystyrene) resin.13 The efficiency
of neutralization was monitored by 1H NMR.
After neutralization, it was found that the chemical
shifts for H-5 (S-CH, singlet) for the aminothiazole
hydrobromide salts 7, 8, 9 (d 7.24, 7.03, 7.34 ppm)
were shifted upfield (d 7.02, 6.73, and 7.10 ppm) in
free-based aminothiazoles 16, 17, 18. Protons for the
NH2 group for free-based aminothiazoles 16, 17, 18
were also found to be broad singlets (d 7.05, 6.91, and
7.03 ppm), which was also diagnostic of the extent of
neutralization. Results summarizing the preparation
of free-based 2-aminothiazoles are provided in
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