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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707533Generated: October 30, 2026

Heptane → (S)-2-hydroxy-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/707533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHeptaneHCID 8900—
ReactantD-Tartaric acidHCID 439655—
ReactantBortezomib boronic anhydrideHCID 60071654—
SolventAcetoneHCID 180—
Product(S)-2-hydroxy-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 acidHCID 67175124547%

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 (0.180 g, 0.164 mmol) and D-tartaric acid (147.5 mg, 0.33 mmol) were mixed in acetone (4 mL). The mixture was heated to form a solution. The solution was cooled uncontrolled until the internal temperature was about 25° C. Heptane (8 mL) was added. The mixture was evaporated to yield (S)-2-hydroxy-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 (0.447 g) which also contained a dimeric species. MS (m/z) in CH3CN: [M+H] calculated for C23H28BN408, 499.2000. found, 499.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09175017B2
Source datasetuspto-grants-2015_11
ORD IDord-7c0c4d65d20a4259ba019b96bf027566
Source noteuspto-grants-2015_11