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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060025Generated: October 31, 2026

Cyanamide → N-cyano-4-(4-methoxypyridin-2-yl)-2-nitroaniline

https://huagongshe.com/reaction/1060025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Chloro-4-(4-methoxypyridin-2-yl)-2-nitrobenzeneHCID 18667563—
SolventDimethylformamideHCID 6228—
ProductN-cyano-4-(4-methoxypyridin-2-yl)-2-nitroanilineHCID 1866749889.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of cyanamide (101 mg) in N,N-dimethylformamide (15 ml) was added sodium hydride (60% dispersion in mineral oil, 90 mg), and the resultant suspension was stirred at ambient temperature for 30 minutes. To the suspension was added 1-chloro-4-(4-methoxypyridin-2-yl)-2-nitrobenzene (264 mg), and the mixture was stirred at 80° C. for 4 hours. The mixture was poured into a saturated aqueous ammonium chloride solution and extracted with ethyl acetate three times. The combined organic layer was washed with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was triturated with diisopropyl ether, filtered and dried under reduced pressure to give N-cyano-4-(4-methoxypyridin-2-yl)-2-nitroaniline (241 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521643B1
Source datasetuspto-grants-2003_02
ORD IDord-9ddb66a6987e4c3a98f13b59cef3053b
Source noteuspto-grants-2003_02