Improved Tag-Assisted Liquid-Phase Peptide Synthesis: Application to the Synthesis of the Bradykinin Receptor Antagonist Icatibant Acetate

A cost- and time-effective synthetic method is a prerequisite to producing therapeutic peptides on a commercial scale. Herein we demonstrate that a soluble-tag-assisted liquid-phase peptide synthesis (LPPS) using a hydrophobic benzyl alcohol as a support is applicable to the 100 g scale production o...

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Veröffentlicht in:Organic process research & development 2019-11, Vol.23 (11), p.2576-2581
Hauptverfasser: Okada, Yohei, Takasawa, Rico, Kubo, Daisuke, Iwanaga, Natsumi, Fujita, Shuji, Suzuki, Kosuke, Suzuki, Hideaki, Kamiya, Hidehiro, Chiba, Kazuhiro
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container_end_page 2581
container_issue 11
container_start_page 2576
container_title Organic process research & development
container_volume 23
creator Okada, Yohei
Takasawa, Rico
Kubo, Daisuke
Iwanaga, Natsumi
Fujita, Shuji
Suzuki, Kosuke
Suzuki, Hideaki
Kamiya, Hidehiro
Chiba, Kazuhiro
description A cost- and time-effective synthetic method is a prerequisite to producing therapeutic peptides on a commercial scale. Herein we demonstrate that a soluble-tag-assisted liquid-phase peptide synthesis (LPPS) using a hydrophobic benzyl alcohol as a support is applicable to the 100 g scale production of therapeutic peptides using the bradykinin receptor antagonist icatibant acetate as a model. The use of sacrificial propylamine to trap the activated amino acids enables one-pot sequential couplings and deprotections without detectable double hits. With the modified procedure, precipitations at every other step are sufficient for the overall process, significantly reducing the amount of MeCN required. The complete consumption of starting materials (99%).
doi_str_mv 10.1021/acs.oprd.9b00397
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title Improved Tag-Assisted Liquid-Phase Peptide Synthesis: Application to the Synthesis of the Bradykinin Receptor Antagonist Icatibant Acetate
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