HCID 21298739, compound → 2-[2-(2,2,2-Trifluoroethyl)-guanidino]-4-(4-aminobutyl)thiazole

HRID 1902263Notes

Reaction equation

HRID 1902263 reaction equation
ClCC(=O)CCCC[N:8]1[C:12](=O)[C:11]2=[CH:14][CH:15]=[CH:16][CH:17]=C2C1=O.[F:20][C:21]([F:31])([F:30])[CH2:22][NH:23][C:24]([NH:26][C:27]([NH2:29])=[S:28])=[NH:25]>C(O)C>[F:31][C:21]([F:20])([F:30])[CH2:22][N:23]=[C:24]([NH2:25])[NH:26][C:27]1[S:28][CH:17]=[C:16]([CH2:15][CH2:14][CH2:11][CH2:12][NH2:8])[N:29]=1

Participants

4

Procedure

To a solution of N-(6-chloro-5-oxohexyl)phthalimide (3.4 g.) in ethanol was added N-(2,2,2-trifluoroethylamidino)-thiourea (2.75 g.) in ethanol (30 ml.). The mixture was heated under reflux for 2 hours and the reaction mixture concentrated to small volume by evaporation. Following treatment of the resulting solution with ether until the solution was just turbid, crystalline 2-[2-(2,2,2-trifluoroethyl)guanidino]-4-(4-phthalimidobutyl)thiazole hydrochloride (3.6 g.) was precipitated. This material (2.1 g.) in ethanol (20 ml.) and water (5 ml.) was heated to boiling and the solution pH was adjusted to 12 by addition of 2 N sodium hydroxide. After heating on a steam bath for 10 minutes, the solution pH was adjusted to 3 with conc. hydrochloric acid and heating continued for a further 0.5 hour. The solution was cooled, adjusted to pH 12 with 2 N sodium hydroxide and extracted with ethyl acetate (2×30 ml.). Evaporation of the washed (H2O), dried (magnesium sulphate) extract gave 2-[2-(2,2,2-trifluoroethyl)guanidino]-4-(4-aminobutyl)-thiazole as a pale yellow gum which was used without further purification.

Workup

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 2 hours
  3. concentrationthe reaction mixture concentrated to small volume by evaporation
  4. customwas precipitated
  5. temperatureThis material (2.1 g.) in ethanol (20 ml.) and water (5 ml.) was heated
  6. additionthe solution pH was adjusted to 12 by addition of 2 N sodium hydroxide
  7. temperatureAfter heating on a steam bath for 10 minutes
  8. temperatureheating
  9. temperatureThe solution was cooled
  10. extractionextracted with ethyl acetate (2×30 ml.)
  11. customEvaporation of the
  12. washwashed (H2O)
  13. dry with materialdried (magnesium sulphate)
  14. extractionextract

Sources & evidence

ORD record
ord-9cdc7035efd1488c99603a79bb18c4ec
Source dataset
uspto-grants-1982_12
Patent number
US04362728

Reaction notes

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