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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397093Generated: November 2, 2026

Water → 3-Morpholino-5-nitropyridin-4-amine

https://huagongshe.com/reaction/1397093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMorpholineHCID 8083—
ReactantEthyl AcetateHCID 8857—
Reactant4-Amino-3-bromo-5-nitropyridineHCID 4997588—
Product3-Morpholino-5-nitropyridin-4-amineHCID 58377913—

Reaction Steps

A solution of 3-bromo-5-nitropyridin-4-amine (XLVI) (1 eq.), in neat morpholine in a sealed tube was heated at 120-140° C. overnight. The solution was poured into a mixture of EtOAc and water. The organic layer was separated. The aqueous layer was extracted with EtOAc. The combined organic layers was washed with brine, dried over MgSO4 and concentrated to get a residue. The crude product was purified on a silica gel column eluting with chloroform:MeOH gradient. The fractions containing product were mixed and concentrated under vacuum. The residue was triturated with hexane to give 3-morpholino-5-nitropyridin-4-amine (LIII).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901150B2
Source datasetuspto-grants-2014_12
ORD IDord-a840f538822e494a9dde57fde0d9d5d4
Source noteuspto-grants-2014_12