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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410219Generated: October 25, 2026

2-Chlorobenzoxazole → N-(4-(3-Bromopyridin-2-yloxy)phenyl)benzo[D]oxazol-2-amine

https://huagongshe.com/reaction/410219

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
Reactant4-(3-Bromopyridin-2-yloxy)benzenamineHCID 57756256—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-(4-(3-Bromopyridin-2-yloxy)phenyl)benzo[D]oxazol-2-amineHCID 59327040—

Reaction Conditions

Temperature170 °C

Reaction Steps

A mixture of 4-(3-bromopyridin-2-yloxy)aniline (1.73 g, 6.53 mmol) and 2-chlorobenzoxazole (1.00 g, 6.51 mmol, TCI America) in NMP (3 mL) was sealed in a screw-cap flask and heated at 170° C. for 20 h. The reaction was cooled to rt and partitioned with water/EtOAc. The aqueous layer was extracted with EtOAc (3×) and the combined organic layers were evaporated onto silica gel and purified by flash chromatography (Isco (80 gram)) eluting with EtOAc:hexanes (0:1→1:2) a tan amorphous solid. MS (ESI, pos. ion) m/z: 382.0, 383.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759532B2
Source datasetuspto-grants-2014_06
ORD IDord-0a1c26e21c5b4b2c8cab14aeba7d1d3d
Source noteuspto-grants-2014_06