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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817034Generated: October 31, 2026

Triethylamine → HCID 178467172, compound

https://huagongshe.com/reaction/1817034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
ReactantHCID 178461678HCID 178461678—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178467172HCID 17846717233%

Reaction Conditions

Temperature80 °C

Reaction Steps

An oven-dried 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), and (Ph3P)4Pd (0.07 equiv). The bottle was covered with a sheet of Parafilm and purged with nitrogen for 5 min, and anhydrous dioxane (13 volume equivalents), triethylamine (3.0 equiv), and tributyl(1-ethoxyvinyl)stannane (1.5 equiv) were added by syringe. The resulting mixture was heated to 80° C. overnight. The reaction was quenched with 1 N KHSO4 and stirred for 30 min. The mixture was then diluted with EtOAc, washed twice with NaHCO3 and once with brine. The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Biotage MPLC 10%-66% EtOAc/Hexanes) provided the title compound (33%) as a white solid. LCMS m/z (APCI)=283.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598248B2
Source datasetuspto-grants-2009_10
ORD IDord-c1b626d454d6442f81a253e9330ebc9a
Source noteuspto-grants-2009_10