Aluminium lithium hydride → (2R,5S)-1-(4-fluorobenzyl)-2-(hydroxy)methyl-5-methylpiperazine

HRID 1861846Notes

Reaction equation

HRID 1861846 reaction equation
[F:1][C:2]1[CH:19]=[CH:18][C:5]([CH2:6][N:7]2[C:12](=O)[C@H:11]([CH3:14])[NH:10][C:9](=O)[C@H:8]2[CH2:16][OH:17])=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[F:1][C:2]1[CH:19]=[CH:18][C:5]([CH2:6][N:7]2[CH2:12][C@H:11]([CH3:14])[NH:10][CH2:9][C@@H:8]2[CH2:16][OH:17])=[CH:4][CH:3]=1

Participants

4

Reactant 2

HCID 21226445Aluminium lithium hydrideHCID 57116208(2R,5S)-1-(4-fluorobenzyl)-2-(hydroxy)methyl-5-methylpiperazine-3,6-dione

Product 1

HCID 57226061(2R,5S)-1-(4-fluorobenzyl)-2-(hydroxy)methyl-5-methylpiperazineYield 90%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a suspension of (2R,5S)-1-(4-fluorobenzyl)-2-(hydroxy)methyl-5-methyl-piperazine-3,6-dione (2.0 g, 7.5 mmol) in anhydrous tetrahydrofuran (50 mL) under N2 at 0° C. was carefully added lithium aluminum hydride (2.2 g, 60 mmol). The resulting suspension was heated to reflux. After 15 hours, the mixture was cooled to ambient temperature and carefully quenched with water (2 mL), then 1 N aqueous KOH solution (6 mL). The resulting suspension was stirred at ambient temperature for 30 minutes, then filtered through Celite (ethyl acetate). The filtrate was concentrated in vacuo to afford 1.6 g (90% yield) of (2R,5S)-1-(4-fluorobenzyl)-2-(hydroxy)methyl-5-methylpiperazine, a compound of formula (S), as a white solid; NMR (CDCl3) 7.3 (dd, 2), 7.0 (dd, 2), 4.2-4.0 (m, 2), 3.5 (d, 1) 3.0 (m, 2), 2.7 (m, 2), 1.7 (m, 1), 1.0 (d, 3).

Workup

  1. temperatureThe resulting suspension was heated to reflux
  2. customcarefully quenched with water (2 mL)
  3. filtrationfiltered through Celite (ethyl acetate)
  4. concentrationThe filtrate was concentrated in vacuo

Sources & evidence

ORD record
ord-f044cad872bf42fa9cae7bb1f565175a
Source dataset
uspto-grants-2003_03
Patent number
US06534509B1

Reaction notes

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