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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427041Generated: October 27, 2026

Water → 5-((2-Aminopyridin-4-yl)oxy)-6-(2-ethoxyethoxy)-N-methyl-1H-indole-1-carboxamide

https://huagongshe.com/reaction/1427041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenyl MethylcarbamateHCID 16034—
ReactantSodium hydrideHCID 24758—
Reactant4-((6-(2-Ethoxyethoxy)-1H-indol-5-yl)oxy)pyridin-2-amineHCID 86730343—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-((2-Aminopyridin-4-yl)oxy)-6-(2-ethoxyethoxy)-N-methyl-1H-indole-1-carboxamideHCID 8673034487%

Reaction Steps

50-72% Oily sodium hydride (265 mg) was added to a solution of 4-((6-(2-ethoxyethoxy)-1H-indol-5-yl)oxy)pyridin-2-amine described in Production Example 24-7 (1.92 g, 6.13 mmol) in N,N-dimethylformamide (20 mL) under nitrogen atmosphere at 0° C. The reaction liquid was stirred at the same temperature for 10 minutes. Phenyl methylcarbamate described in Production Example 1-7 (1.20 g, 7.97 mmol) was added to the reaction liquid, and then the mixture was warmed to mom temperature and stirred for 1 hour. Water and ethyl acetate were added to the reaction liquid. The organic layer was washed serially with water and a saturated saline solution and then dried over anhydrous sodium sulfate. The drying agent was separated by filtration and then the filtrate was concentrated under vacuum. The residue was purified with NH silica gel column chromatography (the solution: n-heptane:ethyl acetate=9:1-0:1) to obtain the title compound (1.97 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933099B2
Source datasetuspto-grants-2015_01
ORD IDord-13227ae2ace641cb9464aabe13280709
Source noteuspto-grants-2015_01