HuagongsheHuagongshe Chemistry Print Report · For research reference only
D-Malic acid → 2-((r)-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 | D-Malic acid | HCID 92824 | — |
| Reactant | Bortezomib boronic anhydride | HCID 60071654 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-((r)-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 69037099 | — |
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 (0.305 g, 0.278 mmol) and D-malic acid (130.3 mg, 0.33 mmol) were mixed in acetone (3 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 3 h. The slurry was filtered to collect solid 2-((R)-2-((R)-3-methyl-1-((S)-3-phenyl-2-(pyrazine-2-carboxamido)propanamido)butyl)-5-oxo-1,3,2-dioxaborolan-4-yl)acetic acid (0.410 g, 100%). [M+H] calculated for C23H28BN4O7, 483.2051. found, 483.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09175017B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-a8a678cbfa3a476d853b0b6a4b1ce88e |
| Source note | uspto-grants-2015_11 |