Sodium Hydroxide → Methyl-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-amine

HRID 1017492Notes

Reaction equation

CO[C:3](=O)[NH:4][C:5]1[CH:6]=[N:7][C:8]([N:18]2[CH2:23][CH2:22][O:21][CH2:20][CH2:19]2)=[CH:9][C:10]=1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[CH3:17].[OH-].[Na+]>C1(C)C=CC=CC=1>[CH3:3][NH:4][C:5]1[CH:6]=[N:7][C:8]([N:18]2[CH2:19][CH2:20][O:21][CH2:22][CH2:23]2)=[CH:9][C:10]=1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[CH3:17]

Participants

Conditions

Temperature: 0 °C

Procedure

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-Ale® (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.

Workup

customThe phases were separated
extractionthe aqueous phase extracted with toluene
washThe combined organic extracts were washed with water and brine
dry with materialdried (Na2SO4)
customevaporated
customThe residue was crystallized from n-heptane at −10° C.

Sources & evidence

ORD record: ord-03718ddb805e4f759bc67bc10553ae1b
Source dataset: uspto-grants-2002_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06479483B2

Reaction notes

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