Dimethylformamide → HCID 57811504, compound

HRID 885566Notes

Reaction equation

HRID 885566 reaction equation
[CH3:1][C:2]1[CH:11]=[C:10]([CH3:12])[C:9]2[CH2:8][CH2:7][CH2:6][CH2:5][C:4]=2[C:3]=1[N:13]1[C:17]([C:18]([F:21])([F:20])[F:19])=[N:16][N:15]=[C:14]1[SH:22].Br[CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26].C(=O)([O-])[O-].[K+].[K+].CN(C=O)C>C1COCC1.O>[CH3:1][C:2]1[CH:11]=[C:10]([CH3:12])[C:9]2[CH2:8][CH2:7][CH2:6][CH2:5][C:4]=2[C:3]=1[N:13]1[C:17]([C:18]([F:21])([F:20])[F:19])=[N:16][N:15]=[C:14]1[S:22][CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26]

Participants

7

Reactant 4

HCID 6228DimethylformamideHCID 7748Ethyl bromoacetate2×HCID 11430Potassium CarbonateHCID 178425472HCID 178425472, compound

Product 1

HCID 57811504HCID 57811504, compoundYield 54.2%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Conditions

Temperature
60 °C

Procedure

To a solution of 4-(2,4-Dimethyl-5,6,7,8-tetrahydronaphthalen-1-yl)-5-(trifluoromethyl)-4H-1,2,4-triazole-3-thiol (0.2 g, 0.611 mmol) in THF (2.44 mL) was added ethyl 2-bromoacetate (68 μL, 0.611 mmol) and potassium carbonate (0.17 g, 1.22 mmol), and the mixture heated at 60° C. for 18 hours. The mixture was concentrated, ethyl 2-bromoacetate (68 μL, 0.611 mmol) and DMF (1.2 mL) added, and the mixture heated at 60° C. for 24 hours. Water (40 mL) was added and the mixture extracted with ethyl acetate (2×40 mL). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered, concentrated and purified by SGC (0-50% ethyl acetate/Hexanes) to afford ethyl 2-(4-(2,4-dimethyl-5,6,7,8-tetrahydronaphthalen-1-yl)-5-(trifluoromethyl)-4H-1,2,4-triazol-3-ylthio)acetate as a clear oil (0.137 g, 54%).

Workup

  1. concentrationThe mixture was concentrated
  2. temperaturethe mixture heated at 60° C. for 24 hours
  3. extractionthe mixture extracted with ethyl acetate (2×40 mL)
  4. washThe combined organic extracts were washed with brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. custompurified by SGC (0-50% ethyl acetate/Hexanes)

Sources & evidence

ORD record
ord-4fc3c79b36e648d59475343af2887753
Source dataset
uspto-grants-2012_08
Patent number
US08242154B2

Reaction notes

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