Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182441Generated: October 31, 2026

Hydrochloric Acid → Methyl-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-amine

https://huagongshe.com/reaction/2182441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium HydroxideHCID 14798—
Reactant6-Morpholin-4-yl-4-o-tolyl-pyridin-3-ylamineHCID 15486051—
ReactantAluminium lithium hydrideHCID 21226445—
CatalystTrifluoroacetic acidHCID 6422—
SolventTetrahydrofuranHCID 8028—
ProductMethyl-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-amineHCID 1143755766%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2.24 g (8.3 mmol) 6-morpholin-4-yl-4-o-tolyl-pyridin-3-ylamine in 17 ml trimethyl orthoformate and 3 drops trifluoroacetic acid was heated for 2 h at 130° C. The reaction mixture was evaporated and dried in vacuo for 30 min. The residual oil was dissolved in 5 ml tetrahydrofuran and was added dropwise under ice cooling to 630 mg (16.6 mmol) lithium aluminum hydride in 20 ml tetrahydrofuran. The reaction mixture was stirred for 1h at room temperature, cooled to 0° C. again and acidified (pH 1-2) by addition of 28% hydrochloric acid solution. After stirring for 5 min, 28% sodium hydroxide solution was added to reach pH 10. The solution was filtered over celite, evaporated and purified by flash chromatography to give 1.56 g (66%) of the title compound as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897226B2
Source datasetuspto-grants-2005_05
ORD IDord-3d3d00ed74e749569a2c67c4232aa575
Source noteuspto-grants-2005_05