Water → HCID 67714290, compound

HRID 264383Notes

Reaction equation

HRID 264383 reaction equation
[CH3:1][O:2][C:3]1[CH:25]=[CH:24][C:6]2=[CH:7][CH:8]=[C:9]3[C:13]([N:12]([CH2:14][C@@H:15]([NH:17]C(=O)C(F)(F)F)[CH3:16])[CH:11]=[CH:10]3)=[C:5]2[CH:4]=1.[OH-:26].[K+].[OH-:28].[Na+].[OH2:30]>CO>[C:3]([OH:2])(=[O:30])/[CH:25]=[CH:24]/[C:6]([OH:28])=[O:26].[CH3:1][O:2][C:3]1[CH:25]=[CH:24][C:6]2=[CH:7][CH:8]=[C:9]3[C:13]([N:12]([CH2:14][C@@H:15]([NH2:17])[CH3:16])[CH:11]=[CH:10]3)=[C:5]2[CH:4]=1

Participants

6

Procedure

A mixture of 1.2 g of (S)-N-[2-(8-methoxy-1H-benz[g]indol-1-yl)-1-methyl-ethyl]-trifluoracetamide, 1.2 g of potassium hydroxide in 3 ml of water and 50 ml of methanol was boiled under reflux for 3 hours. The reaction mixture was subsequently poured into 100 ml of 1N sodium hydroxide solution, extracted twice with 100 ml of diethyl ether each time and once with 100 ml of ethyl acetate, the combined organic phases were washed once with 150 ml and dried over magnesium sulfate. After concentration in a vacuum, the residue was dissolved in 100 ml of anhydrous diethyl ether, filtered and treated while stirring with a solution of 398 mg of fumaric acid in 30 ml of methanol. The mixture was stirred at room temperature for 16 hours and the white crystals were subsequently filtered off. 780 mg (73%) of (S)-2-(8-methoxy-1H-benz[g]indol-1-yl)-1-methyl-ethylamine fumarate (1:0.5) with m.p. 208° were obtained.

Workup

  1. temperatureunder reflux for 3 hours
  2. extractionextracted twice with 100 ml of diethyl ether each time
  3. washonce with 100 ml of ethyl acetate, the combined organic phases were washed once with 150 ml
  4. dry with materialdried over magnesium sulfate
  5. concentrationAfter concentration in a vacuum
  6. dissolutionthe residue was dissolved in 100 ml of anhydrous diethyl ether
  7. filtrationfiltered
  8. additiontreated
  9. stirringThe mixture was stirred at room temperature for 16 hours
  10. filtrationthe white crystals were subsequently filtered off

Sources & evidence

ORD record
ord-47db84cee3e54220b99a0d9e4b85408d
Source dataset
uspto-grants-1997_07
Patent number
US05646173

Reaction notes

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