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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707678Generated: October 30, 2026

L-Malic Acid → 2-((s)-2-((r)-3-Methyl-1-((s)-3-phenyl-2-(pyrazine-2-carboxamido)propanamido)butyl)-5-oxo-1,3,2-dioxaborolan-4-yl)acetic acid

https://huagongshe.com/reaction/707678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Malic AcidHCID 222656—
ReactantBortezomib boronic anhydrideHCID 60071654—
SolventTetrahydrofuranHCID 8028—
Product2-((s)-2-((r)-3-Methyl-1-((s)-3-phenyl-2-(pyrazine-2-carboxamido)propanamido)butyl)-5-oxo-1,3,2-dioxaborolan-4-yl)acetic acidHCID 69038254—

Reaction Steps

A mixture of N,N′,N″-(boroxin-2,4,6-triyltris{[(1R)-3-methylbutane-1,1-diyl]imino[(2S)-1-oxo-3-phenylpropane-1,2-diyl]})tripyrazine-2-carboxamide (0.500 g, 0.455 mmol) and L-malic acid (213.6 mg, 0.55 mmol) were mixed in THF (5 mL). The mixture was heated to form a solution. The solution was cooled uncontrolled until the internal temperature was about 25° C. White solid precipitated out and the resultant slurry was agitated at ambient temperature for 1 h. The slurry was filtered to collect solid 2-((S)-2-((R)-3-methyl-1-((S)-3-phenyl-2-(pyrazine-2-carboxamido)propanamido)butyl)-5-oxo-1,3,2-dioxaborolan-4-yl)acetic acid (0.625 g, 95%). MS (m/z) in CH3CN: [M+H] calculated for C23H28BN4O7, 483.2051. found, 483.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09175018B2
Source datasetuspto-grants-2015_11
ORD IDord-195f893fa6e74507a369853ea1c33977
Source noteuspto-grants-2015_11