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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066922Generated: October 31, 2026

Triethylamine → HCID 178467172, compound

https://huagongshe.com/reaction/2066922

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 anhydous 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 numberUS08293761B2
Source datasetuspto-grants-2012_10
ORD IDord-dfc42833827f4a0c9df129c61968c958
Source noteuspto-grants-2012_10