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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272176Generated: October 30, 2026

Ethyl Acetate → 5-(5-Chlorobenzoxazol-6-yl)-2-pyridylamine

https://huagongshe.com/reaction/2272176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amineHCID 2756555—
Reactant6-Bromo-5-chlorobenzoxazoleHCID 58487277—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Solvent1,4-DioxaneHCID 31275—
Product5-(5-Chlorobenzoxazol-6-yl)-2-pyridylamineHCID 5848691167.4%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 6-bromo-5-chlorobenzoxazole (30) (232 mg, 1 mmol), 2-aminopyridine-5-boronic acid pinacol ester (11) (220 mg, 1 mmol), Bis(di-tret-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium (11) (A-Phos) (70 mg, 0.1 mmol) and K3PO4 (212 mg, 1 mmol) in 2 ml ACN, 2 ml dioxane, 0.5 ml H2O was bubbled with argon before heated at 85° C. for 2 h. After cooling down to r.t., the reaction mixture was taken up in ethyl acetate, washed with aq. NaHCO3 and brine, dried over Na2SO4, concentrated to dryness. The resulting red solid was dissolved in DCM and subjected to silica gel column purification using 0-100% B (A: hexane; B: EA) to furnish 165.6 mg 31 as an orange solid (yield: 67.4%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120751B2
Source datasetuspto-grants-2015_09
ORD IDord-4c5847c38a874207b570eb5597aec87b
Source noteuspto-grants-2015_09