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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508476Generated: October 29, 2026

Sodium Hydroxide → N'-[6-(2,4-Dichloro-phenoxy)-pyridin-3-yl]-N-ethyl-N-methyl-formamidine

https://huagongshe.com/reaction/508476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-ethyl-N-methylformamideHCID 350667—
Reactant6-(2,4-Dichlorophenoxy)pyridin-3-amineHCID 735776—
SolventDichloromethaneHCID 6344—
ProductN'-[6-(2,4-Dichloro-phenoxy)-pyridin-3-yl]-N-ethyl-N-methyl-formamidineHCID 2515851448.8%

Reaction Steps

In a 25 ml single-necked round-bottomed flask, ethylmethylformamide (350 mg) is solubilized in dry dichloromethane (4 ml) at ambient temperature (colourless solution). Under stirring phosphorous oxide chloride (0.4 ml) is added dropwise by syringe. Stirring at ambient temperature is continued for 1 hour. To this solution, 6-(2,4-Dichloro-phenoxy)-pyridin-3-ylamine (0.5 g) dissolved in 1.0 ml of dry dichloromethane is added dropwise by syringe, giving a yellow solution. Stirring is continued at an ambient temperature for 1 hour. The mixture is then poured into ice/water (pH=2, water phase). 2 M aqueous NaOH is then added to get a pH of about 11 and stirring is continued for 10 minutes. The mixture is then extracted with dichloromethane (2×50 ml). The combined organic phases are then dried over sodium sulfate, filtered and the solvent is removed in vacuo. Purification by flash chromatography over silica gel with hexane/ethyl acetate 3:4 (v:v) gives 0.31 g of the compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096525B2
Source datasetuspto-grants-2015_08
ORD IDord-b4aba6412d5443dabfb7da7349f02e8a
Source noteuspto-grants-2015_08