Pyridine → HCID 54156684, compound

HRID 1580610Notes

Reaction equation

HRID 1580610 reaction equation
[CH2:1]([O:3][C:4](=[O:28])[CH2:5][N:6]1[C:12]2[CH:13]=[CH:14][C:15]([C:17]([F:20])([F:19])[F:18])=[CH:16][C:11]=2[C:10]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[N:9][CH2:8][C:7]1=O)[CH3:2].P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:30].N1C=CC=CC=1>C(Cl)Cl.O>[CH2:1]([O:3][C:4](=[O:28])[CH2:5][N:6]1[C:12]2[CH:13]=[CH:14][C:15]([C:17]([F:20])([F:19])[F:18])=[CH:16][C:11]=2[C:10]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[N:9][CH2:8][C:7]1=[S:30])[CH3:2]

Participants

5

Procedure

A mixture of 0.01 mole of 7-trifluoromethyl-2,3dihydro-2-oxo-5-phenyl-1H-1,4-benzodiazepin-1-acetic acid ethyl ester and 0.0105 mole of phosphorus pentasulfide and 100 ml. of pyridine is heated under reflux for about 24 hours. The mixture is evaporated and the residue thus obtained is dissolved in methylene chloride-water. The organic layer is separated, washed with saturated sodium bicarbonate solution, dried over anhydrous magnesium sulfate and evaporated to remove the solvent. The residue thus obtained is chromatographed on silica gel and eluted to give 2,3-dihydro-5-phenyl-2-thioxo-7-(trifluoromethyl)-1H-1,4-benzodiazepin-1-acetic acid ethyl ester.

Workup

  1. temperatureunder reflux for about 24 hours
  2. customThe mixture is evaporated
  3. customthe residue thus obtained
  4. customThe organic layer is separated
  5. washwashed with saturated sodium bicarbonate solution
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customevaporated
  8. customto remove the solvent
  9. customThe residue thus obtained
  10. customis chromatographed on silica gel
  11. washeluted

Sources & evidence

ORD record
ord-d6331036bdb3403e980d27d16d879b4d
Source dataset
uspto-grants-1976_01
Patent number
US03933816

Reaction notes

Loading…