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
Participants
| Role | Name | HCID | Charge |
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| 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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06806370B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-ed09f15569b74532ab848cff6fac6ce4 |
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| Source note | uspto-grants-2004_10 |
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