Acetonitrile → Xrd 489

HRID 1165542Notes

Reaction equation

HRID 1165542 reaction equation
Cl[S:2]([C:5]1[N:15]=[C:8]2[N:9]=[C:10]([CH3:14])[CH:11]=[C:12]([CH3:13])[N:7]2[N:6]=1)(=[O:4])=[O:3].C(#N)C.C[Si](C)(C)[NH:21][C:22]1[C:27]([Cl:28])=[CH:26][CH:25]=[CH:24][C:23]=1[Cl:29]>N1C=CC=CC=1>[Cl:28][C:27]1[CH:26]=[CH:25][CH:24]=[C:23]([Cl:29])[C:22]=1[NH:21][S:2]([C:5]1[N:15]=[C:8]2[N:9]=[C:10]([CH3:14])[CH:11]=[C:12]([CH3:13])[N:7]2[N:6]=1)(=[O:4])=[O:3]

Participants

5

Reactant 3

HCID 6342AcetonitrileHCID 6112325,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-sulfonyl chlorideHCID 143626792,6-Dichloro-N-trimethylsilylaniline

Product 1

HCID 179147Xrd 489Yield 77.2%

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent2×

Conditions

Temperature
65 °C

Procedure

A solution consisting of 102.4 mg (0.415 mmole) of 2-chlorosulfonyl-5,7-dimethyl-1,2,4-triazolo[1,5-a]pyrimidine, 2.0 ml of acetonitrile, and 33.6 μl (0.415 mmole) of pyridine was stirred 5 minutes. N-trimethylsilyl-2,6-dichloroaniline, 86.9 μl (0.456 mmole) was added. The solution was stirred at room temperature for 16 hours and the reaction monitored by thin layer chromatography and by reverse phase HPLC. The 2-chlorosulfonyl compound gradually disappeared and a new peak appeared. The reaction was about 10-30 percent complete after 16 hours. An additional 33.6 μl of pyridine was added and the solution heated at 65° C. for 4 hours and at reflux for 16 hours. The solvent was removed under nitrogen and the residue treated with 4 ml of 0.5N NaOH and stirred for 0.5 hour. The solution was extracted with CH2Cl2, acidified with concentrated HCl and filtered. The precipitate was washed with water and dissolved in CH3CN. The resulting solution was heated to reflux, filtered through silica gel and the solvent removed in vacuo to obtain 119 mg (0.321 mmole, 77.2 percent yield) of N-(2,6-dichlorophenyl)-5,7-dimethyl-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide as a light yellow solid. The product was further purified by washing with acetone, and recrystallizing from refluxing CH3CN to obtain 91.5 mg (0.246 mmole) of product as a white powder, m.p. 263°-265° C.

Workup

  1. stirringThe solution was stirred at room temperature for 16 hours
  2. customcomplete after 16 hours
  3. temperatureat reflux for 16 hours
  4. customThe solvent was removed under nitrogen
  5. additionthe residue treated with 4 ml of 0.5N NaOH
  6. stirringstirred for 0.5 hour
  7. extractionThe solution was extracted with CH2Cl2
  8. filtrationfiltered
  9. washThe precipitate was washed with water
  10. dissolutiondissolved in CH3CN
  11. temperatureThe resulting solution was heated
  12. temperatureto reflux
  13. filtrationfiltered through silica gel
  14. customthe solvent removed in vacuo

Sources & evidence

ORD record
ord-fd6ed164dcb9408d85303e5c92c72cc4
Source dataset
uspto-grants-1990_03
Patent number
US04910306

Reaction notes

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