Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019713Generated: October 25, 2026

Triethylamine → HCID 178439563, compound

https://huagongshe.com/reaction/1019713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantStannane, tributyl-(1Z)-1-propen-1-yl-HCID 5315049—
ReactantHCID 178461678HCID 178461678—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
ProductHCID 178439563HCID 17843956354%

Reaction Conditions

Temperature120 °C

Reaction Steps

A thick-walled microwave bottle 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 (0.12 equiv). The bottle was covered with a sheet of Parafilm and purged with nitrogen for 5 min, and N-methylpyrrolidone (14 volume equivalents), triethyl amine (2.0 equiv), and (E)-tributyl(prop-1-enyl)stannane (3.0 equiv) were added by syringe. The resulting mixture was immediately fitted with a septum and cap and heated to 120° C. in a microwave for 20 min. The reaction was then diluted with EtOAc, washed four times with saturated aq. NaHCO3 and once with brine. The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo. Reverse-phase preparative HPLC provided the title compound (54%) as a 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-780f4ff5d36941739fb705c35c350ce1
Source noteuspto-grants-2014_05