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La solution est refroidie à 40°C puis 5 mL de potasse (10% eq) sont ajoutés. L'agitation est maintenue pendant 2 heures à température ambiante. La phase aqueuse est extraite avec du n-hexane (3 x 100 mL), les phases organiques sont regroupées, séchées sur sulfate de sodium puis évaporées à sec sous pression réduite pour conduire ,
10-tris(tert-butoxycarbonylméthyl)-1,4,7,10- tétraazacyclododécan-1-yl)propan-1-aminium ,
10-tris(carboxyméthyl)-1,4,7,10-tétraazacyclododécan-1- yl)propan-1-aminium ,
500 mg, 0,72 mmol) est mis en suspension dans l'éther éthylique HCl 3M. La suspension est agitée pendant 3 heures à température ambiante puis filtrée ,
excès de carbonate de potassium est éliminé par filtration. L'huile pâteuse, obtenue après évaporation, est triturée successivement avec du toluène (2 x 40 mL) et de l'éther éthylique (2 x 40 mL) pour éliminer le réactif de départ 58 n'ayant pas réagi mmol après évaporation), p.62 ,
mmol) est mis en suspension dans l'éther éthylique HCl 3M. La suspension est agitée pendant 3 heures à température ambiante puis filtrée, Le résidu solide obtenu est lavé avec l'éther éthylique (3 x 20 mL) pour conduire à la forme chlorhydrate du composé, p.61, 2019. ,
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