HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019715Generated: October 25, 2026
(Z)-Prop-1-en-1-ylboronic acid → HCID 178439564, compound
https://huagongshe.com/reaction/1019715
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Z)-Prop-1-en-1-ylboronic acid | HCID 5355539 | — |
| Reactant | HCID 178461678 | HCID 178461678 | — |
| Product | HCID 178439564 | HCID 178439564 | 63% |
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), (Z)-prop-1-enyl boronic acid (2.0 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 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 (63%) as an off-white foam. LCMS m/z (APCI)=281.1 (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-cada75ad2ad64e5fae809388d65267b8 |
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| Source note | uspto-grants-2014_05 |
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