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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044124Generated: October 31, 2026

2-Chloro-3-nitropyridine → HCID 58577473, compound

https://huagongshe.com/reaction/1044124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-3-nitropyridineHCID 79613—
Reactant2-(p-Aminoanilino)benzoxazoleHCID 459105—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 58577473HCID 5857747343.5%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of N-(1,3-benzoxazol-2-yl)benzene-1,4-diamine (0.50 g) and 2-chloro-3-nitropyridine (0.352 g) in NMP (3.0 mL) was stirred at 140° C. for 1.5 h. After this time, the reaction mixture was cooled to ambient temperature, diluted with water (50 mL), and extracted with ethyl acetate (3×100 ml). The combined organic extracts were washed with brine (100 mL), dried (Na2SO4), filtered and concentrated under reduced pressure. The residue obtained was purified by chromatography (silica, methylene chloride to 1:9 ethyl acetate/methylene chloride) to afford N-(1,3-benzoxazol-2-yl)-N′-(3-nitropyridin-2-yl)benzene-1,4-diamine (0.335 g) as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563575B2
Source datasetuspto-grants-2013_10
ORD IDord-1965553543304bd7883d287e861ff902
Source noteuspto-grants-2013_10