Aluminium lithium hydride → HCID 21912213, compound
Reaction equation
Br[C:2]1[CH:23]=[C:22]([CH3:24])[C:5]([O:6][C:7]2[C:12]([CH2:13]O)=[C:11]([NH:15][CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])[CH:10]=[C:9]([CH3:21])[N:8]=2)=[C:4]([CH3:25])[CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1.C(OCC)C.[Cl-].[Al+3].[Cl-].[Cl-]>[CH3:24][C:22]1[CH:23]=[CH:2][CH:3]=[C:4]([CH3:25])[C:5]=1[O:6][C:7]1[C:12]([CH3:13])=[C:11]([NH:15][CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])[CH:10]=[C:9]([CH3:21])[N:8]=1Participants
Procedure
To a solution of [2-(4-bromo-2,6-dimethyl-phenoxy)-4-(1-ethyl-propylamino)-6-methyl-pyridin-3-yl]-methanol (43 mg, 0.106 mmol) in dry THF was added 1.0M lithium aluminum hydride in diethyl ether (0.25 ml) and aluminum chloride (28 mg). The resulting mixture was stirred at room temperature overnight. The mixture was quenched with water, 2NaOH, then water. Solid formed and filtered through celite, washed with THF, then chloroform. The filtrate was concentrated to dryness. The residue was diluted with water and ethyl acetate. The organic layer was separated, dried and concentrated to give the crude material. The title compound was isolated after silca gel chromatography. 1H NMR(CDCl3) d 6.9-7.1(m,3H), 6.07(s,1H), 3.35(d,1H), 3.33(m,1H), 2.14(s,3H), 2.13(s,3H), 2.12(s,6H), 1.5-1.8(m,4H), 0.97(t,6H) ppm.
Workup
- customThe mixture was quenched with water, 2NaOH
- customSolid formed
- filtrationfiltered through celite
- washwashed with THF
- concentrationThe filtrate was concentrated to dryness
- additionThe residue was diluted with water and ethyl acetate
- customThe organic layer was separated
- customdried
- concentrationconcentrated
- customto give the crude material
Sources & evidence
- ORD record
- ord-20bb5c5b1201460ca5c3a6bc1ea64940
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06833378B2
Reaction notes
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