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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429877Generated: November 3, 2026

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

https://huagongshe.com/reaction/1429877

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 numberUS08940758B2
Source datasetuspto-grants-2015_01
ORD IDord-156f803677034448a026f915cbf5a2cd
Source noteuspto-grants-2015_01