The present invention relates to a method for synthesizing [ 10 B] LBPA, which is a boron compound used in a new chemotherapy treatment technique, boron neutron capture therapy (BNCT). More specifically, the present invention relates to important intermediates of [B 10] Synthesis and method Synthesis of [B 10] LBPA using the same for the synthesis of pinacolborane. According to the present invention, [ 10 B] LBPA used in clinical tests of BNCT, which is a new chemotherapeutic technique with minimal side effects on normal cells, can be mass-produced with high 10B efficiency and easy synthesis method.
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