Lithium aluminum hydride → HCID 66797914, compound

HRID 1397591Notes

Reaction equation

HRID 1397591 reaction equation
[AlH4-].[Li+].[NH2:3][C@H:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6][C@H:5]1[C:13]([N:15]([CH3:17])[CH3:16])=O>C1COCC1>[CH3:17][N:15]([CH2:13][C@@H:5]1[CH2:6][C:7]2[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=2)[C@@H:4]1[NH2:3])[CH3:16]

Participants

4

Conditions

Temperature
60 °C

Procedure

To a stirred suspension of lithium tetrahydroaluminate (256 mg, 6.74 mmol) in THF (20.0 mL) was added a solution of rel-(1R,2R)-1-amino-N,N-dimethylindane-2-carboxamide (580 mg, 2.70 mmol) in THF (10.0 mL) at 0° C. under an atmosphere of Argon, and then the mixture was stirred for 1 h at 60° C. following by stirring for 14 h at 23° C. The reaction mixture was quenched by addition of water and 1.00 M NaOH (5.00 mL), and the resulting mixture was stirred for 2 h. This suspension was filtered through a Celite pad, and the filtrate was concentrated in vacuo. The residue was purified by flash chromatography (5 to 20% Methanol/DCM with 1% NH4OH) to afford the title compound (438 mg, 95%) as a light brown oil.

Workup

  1. stirringby stirring for 14 h at 23° C
  2. customThe reaction mixture was quenched by addition of water and 1.00 M NaOH (5.00 mL)
  3. stirringthe resulting mixture was stirred for 2 h
  4. filtrationThis suspension was filtered through a Celite pad
  5. concentrationthe filtrate was concentrated in vacuo
  6. customThe residue was purified by flash chromatography (5 to 20% Methanol/DCM with 1% NH4OH)

Sources & evidence

ORD record
ord-39ffc94f952b4f7887f9f0fc035a777e
Source dataset
uspto-grants-2014_12
Patent number
US08901136B2

Reaction notes

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