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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Z)-Prop-1-en-1-ylboronic acidHCID 5355539—
ReactantHCID 178461678HCID 178461678—
ProductHCID 178439564HCID 17843956463%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716291B2
Source datasetuspto-grants-2014_05
ORD IDord-cada75ad2ad64e5fae809388d65267b8
Source noteuspto-grants-2014_05