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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53520Generated: October 26, 2026

Ethylamine → N-(2-Chloro-4-methyl-3-pyridinyl)-2-ethylamino-3-pyridinecarboxamide

https://huagongshe.com/reaction/53520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantHexaneHCID 8058—
Reactant2-Chloro-N-(2-chloro-4-methyl-3-pyridinyl)-3-pyridinecarboxamideHCID 10423868—
SolventO-XyleneHCID 7237—
SolventEthyl AcetateHCID 8857—
ProductN-(2-Chloro-4-methyl-3-pyridinyl)-2-ethylamino-3-pyridinecarboxamideHCID 1106621776.2%

Reaction Conditions

Temperature165 °C

Reaction Steps

Ethylamine (12.7 g) was added to a suspension of 21.0 g of the 2-chloro-N-(2-chloro-4-methyl-3-pyridinyl)-3-pyridinecarboxamide in 150 ml of xylene in a steel bomb. The mixture was then heated in an oil bath to 165° C. for 6 hrs. and then stirred overnight at room temperature. The solvent was removed in vacuo and water added to the residue. The product was extracted with ether, dried (sodium sulfate) and concentrated to give an oil. This was dissolved in ethyl acetate followed by hexane at which time a precipitate formed. The solid was filtered and dried to give 16.5 g of the title compound, m.p. 122°-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620974
Source datasetuspto-grants-1997_04
ORD IDord-6931056261934f4b9e2954d3c9e52c11
Source noteuspto-grants-1997_04