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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427412Generated: October 27, 2026

Potassium Carbonate → 4-(4-Amino-2,3-dichlorophenoxy)-3-nitropyridin-2-amine

https://huagongshe.com/reaction/1427412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-3-nitropyridin-2-amineHCID 4071694—
Reactant4-Amino-2,3-dichlorophenolHCID 9877529—
SolventDimethylformamideHCID 6228—
Product4-(4-Amino-2,3-dichlorophenoxy)-3-nitropyridin-2-amineHCID 6800171172.3%

Reaction Steps

To a stirred solution of 4-amino-2,3-dichlorophenol (1.00 g, 5.62 mmol) in dry DMF (20 mL) under N2 was added K2CO3 (854 mg, 6.18 mmol) and the mixture kept at RT for 10 min and then treated with a solution of 4-chloro-3-nitropyridin-2-amine (1.024 g, 5.90 mmol) in dry DMF (5.0 mL) in a single portion. The reaction mixture was maintained at RT for 19 hr and was then partitioned between EtOAc (100 mL) and water (100 mL). The aq layer was separated and was extracted with EtOAc (4×70 mL) and the combined organic extracts were dried and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, 80 g, EtOAc in isohexane, 0-70%, gradient elution) to afford 4-(4-amino-2,3-dichlorophenoxy)-3-nitropyridin-2-amine as a dark solid (1.28 g, 70%); Rt 1.85 min (Method 2); m/z 315 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933228B2
Source datasetuspto-grants-2015_01
ORD IDord-2e2d8c3ca8ce44b6abdc0621059ba965
Source noteuspto-grants-2015_01