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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53532Generated: October 29, 2026

Ethylamine → N-(2-Bromo-6-methoxy-4-methyl-3-pyridinyl)-2-ethylamino-3-pyridinecarboxamide

https://huagongshe.com/reaction/53532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant1,4-DioxaneHCID 31275—
ReactantN-(2-bromo-6-methoxy-4-methyl-3-pyridinyl)-2-chloro-3-pyridinecarboxamideHCID 19960021—
SolventEthyl AcetateHCID 8857—
ProductN-(2-Bromo-6-methoxy-4-methyl-3-pyridinyl)-2-ethylamino-3-pyridinecarboxamideHCID 1996003244.2%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of N-(2-bromo-6-methoxy-4-methyl-3-pyridinyl)-2-chloro-3-pyridinecarboxamide (2.1 g), dioxane (10 ml), and ethylamine (0.5 g) was heated to 140° C. in a sealed tube for 5 hours. The cooled mixture was diluted with ethyl acetate, washed with water, and the organic phase was dried (anhydrous magnesium sulfate) and concentrated. The product was purified on a silica gel column (methylene chloride/ethyl acetate, 99:1) and crystallized by trituration with diisopropyl ether to give 0.95 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620974
Source datasetuspto-grants-1997_04
ORD IDord-0d2446fa61c7432eb532efde6150e60e
Source noteuspto-grants-1997_04