Water → HCID 19808462, compound

HRID 373811Notes

Reaction equation

HRID 373811 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9]([N:13]1[CH2:18][CH2:17][N:16]([CH2:19][C:20]#[N:21])[CH2:15][CH2:14]1)=[CH:8][CH:7]=[CH:6]2.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[Cl-].[NH4+]>O1CCCC1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9]([N:13]1[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][NH2:21])[CH2:15][CH2:14]1)=[CH:8][CH:7]=[CH:6]2

Participants

6

Procedure

A solution containing 4.2 g of the compound obtained in Stage C, in 25 ml of tetrahydrofuran is added dropwise at room temperature to a suspension, stirred under a nitrogen atmosphere, of 1.1 g of lithium aluminum hydride in 25 ml of tetrahydrofuran. Stirring is maintained for 20 minutes after the addition is complete, and the reaction medium is then hydrolyzed with the requisite quantity of water saturated with ammonium chloride. The precipitate formed is filtered off and washed with tetrahydrofuran, and the filtrates are concentrated under vacuum to yield an oil.

Workup

  1. temperatureis maintained for 20 minutes
  2. additionafter the addition
  3. customThe precipitate formed
  4. filtrationis filtered off
  5. washwashed with tetrahydrofuran
  6. concentrationthe filtrates are concentrated under vacuum
  7. customto yield an oil

Sources & evidence

ORD record
ord-741407a4626c48ae9d67d0b6fe84d99c
Source dataset
uspto-grants-1992_11
Patent number
US05166156

Reaction notes

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