Dimethylformamide → 6-(Trifluoromethyl)imidazo[2,1-b][1,3]thiazole-5-carboxylic acid
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]2Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
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
- customAt 0° C
- temperatureAfter heating for 2.5 d
- temperatureto reflux the mixture
- additionis poured into ice
- extractionextracted three times with DCM
- dry with materialdried over MgSO4
- concentrationconcentrated under reduced pressure
- additionDCM is added
- filtrationthe obtained precipitate is filtered off
- concentrationthe filtrate is concentrated in vacuo
- customto give a crude product which
- stirringthe mixture is stirred for 90 min at RT
- customThe solvents are partially removed in vacuo
- 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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