Ethyl Acetate → HCID 54169012, compound

HRID 2293037Notes

Reaction equation

HRID 2293037 reaction equation
[NH2:1][C:2]1[S:3][CH2:4][CH:5]=[CH:6][N:7]=1.[CH2:8](I)[CH2:9][CH3:10].C(OCC)(=O)C.[OH-].[K+]>CN(C)C=O.CO>[CH2:8]([N:7]1[CH:6]=[CH:5][CH2:4][S:3][C:2]1=[NH:1])[CH2:9][CH3:10]

Participants

7

Conditions

Temperature
50 °C

Procedure

1.3 g (11.4 mmol) of 2-amino-6H-1,3-thiazine was dissolved in 4 ml of dimethylformamide, and 2.4 g (14.1 mmol) of n-propyl iodide was added thereto. The mixture was heated at 50° C. for one hour and then stirred at room temperature overnight. To the reaction solution, 100 ml of ethyl acetate was added, and the mixture was stirred and then left to stand still. Then, the ethyl acetate layer was separated and removed by decantation. Then, the residual oily substance was dissolved in 50 ml of methanol, and 30 ml of a methanol solution containing 0.75 g (11.4 mmol) of 85% potassium hydroxide, was added thereto at room temperature. The mixture was further stirred at the same temperature for one hour, and then methanol was distilled off under reduced pressure. To the residue, 60 ml of chloroform was added, and insoluble matters were removed by filtration. Then, the filtrate was concentrated under reduced pressure. The residual oily substance was purified by alumina column chromatography (eluent: chloroform) to obtain 0.4 g of 3,6-dihydro-3-n-propyl-2H-1,3-thiazin-2-imine as an oily substance.

Workup

  1. stirringthe mixture was stirred
  2. waitleft
  3. customThen, the ethyl acetate layer was separated
  4. customremoved by decantation
  5. dissolutionThen, the residual oily substance was dissolved in 50 ml of methanol
  6. additionwas added
  7. customat room temperature
  8. stirringThe mixture was further stirred at the same temperature for one hour
  9. distillationmethanol was distilled off under reduced pressure
  10. additionTo the residue, 60 ml of chloroform was added
  11. custominsoluble matters were removed by filtration
  12. concentrationThen, the filtrate was concentrated under reduced pressure
  13. customThe residual oily substance was purified by alumina column chromatography (eluent: chloroform)

Sources & evidence

ORD record
ord-1c91ee392a0141f99cf7585177c83083
Source dataset
uspto-grants-1997_11
Patent number
US05686390

Reaction notes

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