Ethanol → HCID 13344905, compound

HRID 1462327Notes

Reaction equation

HRID 1462327 reaction equation
[CH2:1](O)C.C[O-].[Na+].[N:7]1[CH:8]=[CH:9][N:10]2[C:16]=1[CH2:15][C:14]1[CH:17]=[CH:18][CH:19]=[CH:20][C:13]=1[NH:12][C:11]2=[S:21].CI>O>[CH3:1][S:21][C:11]1[N:10]2[CH:9]=[CH:8][N:7]=[C:16]2[CH2:15][C:14]2[CH:17]=[CH:18][CH:19]=[CH:20][C:13]=2[N:12]=1

Participants

6

Reactant 4

HCID 702EthanolHCID 6328Methyl iodideHCID 10942334Sodium MethoxideHCID 1334490411H-imidazo[1,2-c][1,3]benzodiazepine-5(6H)-thione

Product 1

HCID 13344905HCID 13344905, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Absolute ethanol (20,000 ml) was charged into a 20 gallon flask and stirred under nitrogen atmosphere; 517.62 g (9.58 moles) of sodium methoxide were added. After stirring for 30 minutes there was complete solution and 2,063 g (9.58 moles) of 11H-imidazo[1,2-c][1,3]benzodiazepine-5(6H)-thione were added. There was complete solution after stirring at room temperature for 1 hours. The solution was then cooled to 1°, and 1,360 g (9.58 moles) of methyl iodide were added over 30 minutes. The reaction mixture was stirred at 5° for 4 hours and at ambient temperature overnight. The turbid solution was then cooled to 5° and diluted with 50,000 ml of water. The resulting suspension was stirred for 4 hours at 5°. The solid was collected, and dried (5 mm Hg/60°) to give 5-methylthio-11H-imidazo[1,2-c][1,3]benzodiazepine, m.p. 87°-8°.

Workup

  1. stirringAfter stirring for 30 minutes there
  2. additionwere added
  3. stirringafter stirring at room temperature for 1 hours
  4. temperatureThe solution was then cooled to 1°
  5. stirringThe reaction mixture was stirred at 5° for 4 hours and at ambient temperature overnight
  6. temperatureThe turbid solution was then cooled to 5°
  7. stirringThe resulting suspension was stirred for 4 hours at 5°
  8. customThe solid was collected
  9. customdried (5 mm Hg/60°)

Sources & evidence

ORD record
ord-2fe18bcd82d6454fb02443423d1084fa
Source dataset
uspto-grants-1984_07
Patent number
US04460508

Reaction notes

Loading…