Dimethylformamide → 6-(Trifluoromethyl)imidazo[2,1-b][1,3]thiazole-5-carboxylic acid

HRID 2064748Notes

Reaction equation

HRID 2064748 reaction equation
O=P(Cl)(Cl)Cl.CN([CH:9]=[O:10])C.[F:11][C:12]([F:22])([F:21])[C:13]1[N:14]=[C:15]2[N:19]([CH:20]=1)[CH:18]=[CH:17][S:16]2.Cl([O-])=[O:24].[Na+]>C(Cl)(Cl)Cl.C(O)(C)(C)C.O>[F:22][C:12]([F:21])([F:11])[C:13]1[N:14]=[C:15]2[N:19]([C:20]=1[C:9]([OH:10])=[O:24])[CH:18]=[CH:17][S:16]2

Participants

8

Procedure

At 0° C. POCl3 (17.1 mmol) is added dropwise to a solution of DMF (20.6 mmol) in chloroform (5.0 mL). A solution of 6-trifluoromethyl-imidazo[2,1-b]thiazole (3.17 mmol) in chloroform (15 mL) is added dropwise at 0° C. and the mixture is stirred for 3 h at RT. After heating for 2.5 d to reflux the mixture is poured into ice, extracted three times with DCM, dried over MgSO4 and concentrated under reduced pressure. DCM is added, the obtained precipitate is filtered off and the filtrate is concentrated in vacuo to give a crude product which is dissolved in tert.-butanol (19.5 mL). A solution of sodium chlorite (23.0 mmol) and NaH2PO4 (17.6 mmol) in water (19.5 mL) is added dropwise and the mixture is stirred for 90 min at RT. The solvents are partially removed in vacuo and the obtained precipitate is filtered off to give the desired product as a white solid. LC-MS: tR=0.73 min; [M+H]+=237.2.

Workup

  1. customAt 0° C
  2. temperatureAfter heating for 2.5 d
  3. temperatureto reflux the mixture
  4. additionis poured into ice
  5. extractionextracted three times with DCM
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated under reduced pressure
  8. additionDCM is added
  9. filtrationthe obtained precipitate is filtered off
  10. concentrationthe filtrate is concentrated in vacuo
  11. customto give a crude product which
  12. stirringthe mixture is stirred for 90 min at RT
  13. customThe solvents are partially removed in vacuo
  14. filtrationthe obtained precipitate is filtered off

Sources & evidence

ORD record
ord-aeb84cae05154bb5bcacfa55e3480881
Source dataset
uspto-grants-2012_10
Patent number
US08288435B2

Reaction notes

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