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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Morpholin-4-yl-4-o-tolyl-pyridin-3-ylamine | HCID 15486051 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Catalyst | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-amine | HCID 11437557 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06897226B2 |
|---|
| Source dataset | uspto-grants-2005_05 |
|---|
| ORD ID | ord-3d3d00ed74e749569a2c67c4232aa575 |
|---|
| Source note | uspto-grants-2005_05 |
|---|