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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774944Generated: November 1, 2026

Triethylamine → HCID 89689648, compound

https://huagongshe.com/reaction/1774944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-5-bromo-3-methoxypyrazineHCID 11344724—
ReactantMeOH tetrahydrofuranHCID 21899815—
ReactantHCID 178418416HCID 178418416—
ProductHCID 89689648HCID 89689648—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-bromo-3-methoxypyrazin-2-amine (2.80 g, 13.7 mmol, 1 eq.; Jiang, B. et al. Bioorg. Med. Chem. (2001), 9, 1149-1154), [1,1,-Bis-(diphenylphosphino)ferrocen]palladium(II)-dichlorid (2.24 g, 2.75 mmol, 0.2 eq) and triethylamine (2.10 mL, 15.1 mmol, 1.1 eq) was placed in 600 mL autoclave and dissolved in 135 mL methanol/THF (10/1). The autoclave was flushed with carbon monoxide (3×) and was then pressurized with carbon monoxide to 9 bar. After 30 min at r.t. no conversion was obtained. The autoclave was again pressurized with carbon monoxide to 9 bar and subsequently heated to 100° C. In the course of the reaction, carbon monoxide consumption was observed (decrease of CO pressure). The autoclave was cooled to r.t., flushed with inert gas and the reaction mixture was filtered through a small pad of Celite. LC-MS analysis showed full conversion. The volatile components were removed in vacuo and the material observed this way (1.8 g, 62%) contained the title compound in 92% purity (UPLC-MS, area-%) and was used in the following without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260435B2
Source datasetuspto-grants-2016_02
ORD IDord-ae09c76ea42946239599241b61c0618c
Source noteuspto-grants-2016_02