Aluminium lithium hydride → HCID 23627746, compound

HRID 1171910Notes

Reaction equation

HRID 1171910 reaction equation
C[O:2][C:3](=O)[CH2:4][N:5]1[CH2:10][CH2:9][N:8]([C:11]2[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[C:13]([O:19][CH:20]3[CH2:24][CH2:23][CH2:22][CH2:21]3)[CH:12]=2)[CH2:7][C@@H:6]1[CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[CH2:25]([C@H:6]1[CH2:7][N:8]([C:11]2[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[C:13]([O:19][CH:20]3[CH2:21][CH2:22][CH2:23][CH2:24]3)[CH:12]=2)[CH2:9][CH2:10][N:5]1[CH2:4][CH2:3][OH:2])[C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=1

Participants

4

Reactant 2

HCID 21226445Aluminium lithium hydrideHCID 23627745HCID 23627745, compound

Product 1

HCID 23627746HCID 23627746, compoundYield 73.1%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

A solution of [(S)-2-Benzyl-4-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazin-1-yl]-acetic acid methyl ester (Example 57) (110 mg, 0.25 mmol) in THF (2 mL) at room temperature was treated with a 1 N THF solution of lithium aluminum hydride (750 μL, 0.75 mmol) and allowed to stir for 12 h. The reaction mixture was quenched with an aqueous 15% NaOH solution (250 μL) followed by water (250 μL) and THF (2 mL). the reaction mixture was then treated with MgSO4, filtered, and evaporated. The residue was then dissolved in EtOAc (3 mL), retreated with MgSO4, filtered, and evaporated to afford product as an oil (75 mg, 73%). 1H NMR (CDCl3) 1.58-1.62 (m, 2H), 1.67-1.88 (m, 6H), 2.74-3.22 (m, 12H), 3.65-3.76 (m, 2H), 3.78 (s, 3H), 4.64-4.67 (m, 1H), 6.34 (dd, J=8.6, 2.9, 1H), 6.40 (d, J=2.6, 1H), 6.75 (d, J=8.6, 1H), 7.20-7.33 (m, 5H). 13C NMR 24.2 (CH2), 33.0 (CH2), 33.0 (CH2), 48.4 (CH2), 49.7 (CH2), 53.9 (CH2), 55.5 (CH2), 56.9 (CH3), 58.1 (CH2), 61.6 (CH), 80.5 (CH), 106.5 (CH), 108.1 (CH), 113.4 (CH), 126.5 (CH) 128.8 (CH), 129.5 (CH), 139.6, 144.7, 146.5, 148.5. LC/MS 4.81 min, [M+1]+ 411.

Workup

  1. customThe reaction mixture was quenched with an aqueous 15% NaOH solution (250 μL)
  2. additionthe reaction mixture was then treated with MgSO4
  3. filtrationfiltered
  4. customevaporated
  5. dissolutionThe residue was then dissolved in EtOAc (3 mL)
  6. filtrationfiltered
  7. customevaporated

Sources & evidence

ORD record
ord-081f374687f647e9926766f7528363c9
Source dataset
uspto-grants-2010_11
Patent number
US07829713B2

Reaction notes

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