Water → HCID 54207545, compound

HRID 1417465Notes

Reaction equation

HRID 1417465 reaction equation
[H-].C([Al+]CC(C)C)C(C)C.[CH2:11]([N:18]1[C:30]2[C:29]([CH3:31])=[C:28]([C:32](OCC)=[O:33])[CH:27]=[CH:26][C:25]=2[C:24]2[C:19]1=[CH:20][CH:21]=[CH:22][CH:23]=2)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.O.[OH-].[Na+]>CCCCCC.C(Cl)Cl>[CH2:11]([N:18]1[C:30]2[C:29]([CH3:31])=[C:28]([CH:32]=[O:33])[CH:27]=[CH:26][C:25]=2[C:24]2[C:19]1=[CH:20][CH:21]=[CH:22][CH:23]=2)[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1

Participants

7

Procedure

1.6 ml of a 1.5M solution of diisobutylaluminum hydride in hexane was added at -78° C. to a solution of 213 mg of ethyl 9-benzyl-1-methylcarbazole-2-carboxylate, as obtained in Example 28, in 5 ml of methylene chloride. The reaction mixture was stirred for 1 hour at this temperature, warmed to room temperature, and then stirred for a further 1 hour at room temperature. After this time, 0.1 ml of water, 0.1 ml of a 1N aqueous solution of sodium hydroxide and 0.3 ml of water were added successively to the reaction mixture. Precipitated crystals were filtered off and the filtrate was then concentrated by evaporation under reduced pressure. 187 mg of pyridinium dichromate and molecular sieve 4A, followed by 2 ml of methylene chloride, were added to 100 mg of the thus obtained residue. The resulting mixture was stirred for two hours at room temperature, filtered using Florisil (trade mark), and concentrated by evaporation under reduced pressure. The resulting residue was subjected to column chromatography using 2 g of silica gel with a 5:1 v/v mixture of hexane and ethyl acetate as the eluent, to yield 94 mg of the title compound as an amorphous solid.

Workup

  1. stirringstirred for a further 1 hour at room temperature
  2. customPrecipitated crystals
  3. filtrationwere filtered off
  4. concentrationthe filtrate was then concentrated by evaporation under reduced pressure
  5. additionwere added to 100 mg of the thus obtained residue
  6. stirringThe resulting mixture was stirred for two hours at room temperature
  7. filtrationfiltered
  8. concentrationconcentrated by evaporation under reduced pressure
  9. additionwith a 5:1 v/v mixture of hexane and ethyl acetate as the eluent

Sources & evidence

ORD record
ord-4f869eeb90fd4a1c8a94083fb9d13fc9
Source dataset
uspto-grants-1999_03
Patent number
US05877199

Reaction notes

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