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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500761Generated: October 27, 2026

Potassium Phosphate, Tribasic → 3-(6-Chloropyrazin-2-yl)pyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1500761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
Reactant2,6-DichloropyrazineHCID 78504—
Reactant3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazolo[1,5-a]pyridineHCID 58385948—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
Product3-(6-Chloropyrazin-2-yl)pyrazolo[1,5-a]pyridineHCID 5830348333.1%

Reaction Steps

2,6-Dichloropyrazine (0.316 g, 2.12 mmol), tris(dibenzylideneacetone)dipalladium (0), (0.097 g, 0.106 mmol), tricyclohexylphosphine (0.06 g, 0.212 mmol) and potassium phosphate (1.35 g, 6.36 mmol) were added to a suspension of 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazolo[1,5-a]pyridine (Preparation 27a, 0.518 g, 2.12 mmol)) in N,N′-dimethylformamide (10 mL). This mixture was subjected to microwave irradiation at 100° C. for 40 min. The reaction mixture was filtered through Celite®, eluting with methanol, and the filtrate was evaporated. The resulting residue was purified by flash chromatography (2:8 to 3:7 ethyl acetate/hexane) to yield the title compound (0.162 g, 33%, two steps) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206183B2
Source datasetuspto-grants-2015_12
ORD IDord-f37ecd45dff4442b88a805aa14b296bb
Source noteuspto-grants-2015_12