HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Methyl-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (6-Morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-carbamic acid methyl ester | HCID 12167319 | — |
| Reactant | Red-Al | HCID 16684438 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-amine | HCID 11437557 | 89.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of 3.0 g (9.1 mMol) (6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-carbamic acid methyl ester in 15 ml toluene was added at room temperature over 15 minutes to a solution of 13 ml (46 mMol) Red-Al® (70% in toluene) and 15 ml toluene. After 2 hours at 50° C., the reaction mixture was cooled to 0° C. and 25.5 ml aqueous NaOH 1N were added over 10 minutes (very exothermic). The phases were separated and the aqueous phase extracted with toluene. The combined organic extracts were washed with water and brine, dried (Na2SO4) and evaporated. The residue was crystallized from n-heptane at −10° C. to yield 2.3 g (88%) methyl-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-amine as a light beige powder of m.p.=73.5-76° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06303790B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-dafd3b65630e41e48b2167d2c18ef5d4 |
| Source note | uspto-grants-2001_10 |