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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393373Generated: October 29, 2026

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

https://huagongshe.com/reaction/393373

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 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 1 h 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 numberUS06806370B2
Source datasetuspto-grants-2004_10
ORD IDord-ed09f15569b74532ab848cff6fac6ce4
Source noteuspto-grants-2004_10