HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019716Generated: October 26, 2026
Vinylboronic acid → HCID 178437084, compound
https://huagongshe.com/reaction/1019716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vinylboronic acid | HCID 4683185 | — |
| Reactant | HCID 178461678 | HCID 178461678 | — |
| Product | HCID 178437084 | HCID 178437084 | 54% |
Reaction Steps
A scintillation vial equipped with a stirbar was charged with (S)-6-bromo-1-(1-phenylethyl)-1H-imidazo[4,5-b]pyrazin-2-ol (1.0 equiv), vinyl boronic acid (2.2 equiv), and (DPPF)PdCl2 (0.10 equiv). The vial was fitted with a septum-lined cap and purged with nitrogen for 5-10 min. To this mixture was added dioxane (16.6 volume equivalents) and degassed 2N K2CO3 (4.2 volume equivalents) by syringe. The resulting mixture was heated to 90° C. overnight. The mixture was cooled to room temperature, diluted with 12 volume equivalents EtOAc, washed with twice with saturated aq. NaHCO3, and once with brine. The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Biotage MPLC 5%-40% EtOAc/Hexanes) provided the title compound as an off-white solid (54%). LCMS m/z (APCI)=267.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716291B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-8c93b94abecb499e9cd27670886d312f |
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| Source note | uspto-grants-2014_05 |
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