HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Malic Acid | HCID 222656 | — |
| Reactant | Bortezomib boronic anhydride | HCID 60071654 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 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 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859504B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-40c68971094e4c3db671e7a2ca8b1388 |
| Source note | uspto-grants-2014_10 |