Aluminium lithium hydride → HCID 21912213, compound

HRID 2307965Notes

Reaction equation

HRID 2307965 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]=1

Participants

6

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

  1. customThe mixture was quenched with water, 2NaOH
  2. customSolid formed
  3. filtrationfiltered through celite
  4. washwashed with THF
  5. concentrationThe filtrate was concentrated to dryness
  6. additionThe residue was diluted with water and ethyl acetate
  7. customThe organic layer was separated
  8. customdried
  9. concentrationconcentrated
  10. 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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