Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371972Generated: October 30, 2026

2-Aminopyridine → HCID 21071444, compound

https://huagongshe.com/reaction/1371972

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
Reactant2-(3-Bromophenyl)-1,3-dioxolaneHCID 87306—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 21071444HCID 21071444—

Reaction Steps

Combine 2-aminopyridine (8.25 g, 95 mmol), 2-(3-bromo-phenyl)-[1,3]dioxolane (13.8 mL, 90 mmol), sodium t-butoxide (12.2 g, 126 mmol), BINAP (210 mg, 0.62 mmol), Pd2(dbu)3 (630 mg, 0.21 mmol) and toluene (100 mL) and heat to reflux for 48 hours. Cool the reaction to room temperature, dissolve in ether and filter and concentrate the resulting solution. Purification by flash chromatography (hexanes/EtOAc (8.5:1.5) and then hexanes/EtOAc (7:3)) provides the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157488B2
Source datasetuspto-grants-2007_01
ORD IDord-c02ef4b750af4fb9b42d34bbfe71b8b7
Source noteuspto-grants-2007_01