Trifluoroacetic acid → 5-(Thiophen-2-ylmethyl)imidazole-1-sulfonic acid dimethylamide

1-(Dimethylsulfamoyl)imidazole (1) (2.0 g, 11.4 mmol) is taken up in 42 mL of anhydrous THF and cooled to −78° C. n-BuLi (6.6 mL, 10.6 mmol) is added dropwise to the solution of (1). The resultant solution is stirred at −78° C. for 30 min. Tert-butyldimethylsilylchloride (TBSCl) (1.6 g, 10.6 mmol) in 8 mL of THF is added to the reaction. The reaction is warmed to rt and stirred overnight. The next day the reaction is cooled to −20° C. and 7.3 mL (11.6 mmol) of n-BuLi added. After stirring at −20° C. for 45 min, 3-thiophene carboxaldehyde (2) (1.0 mL, 11.6 mmol) is added to the reaction mixture. Then reaction is warmed to rt and stirred overnight. The next day the reaction is quenched with water and diluted with ethyl acetate. The organic layer is washed with water followed by brine. The organic phase is dried over sodium sulfate and the solvent removed under reduced pressure. Flash chromatography (2:5 ethyl acetate/hexane) affords 3.0 g (7.5 mmol) of 2-(t-butyldimethylsilyl)-5-(hydroxythiophen-2-ylmethyl)imidazole-1-sulfonic acid dimethylamide (3). (3) (1.5 g, 3.74 mmol) is taken up in 37 mL of THF. A 1M solution of tetra-n-butylammonium fluoride (TBAF) in THF (4.1 mL, 4.1 mmol) is added dropwise to the solution of (3). The reaction is stirred overnight at rt. The next day the reaction is quenched with water and then extracted with ethyl acetate. The organic layer is washed with water followed by brine. The organic phase is dried over sodium sulfate and the solvent removed under reduced pressure. 0.94 g (3.3 mmol) of 5-(hydroxythiophen-2-ylmethyl)imidazole-1-sulfonic acid dimethylamide (4) is recovered. (4) (0.5 g, 1.74 mmol) is taken up in 23 mL of dichloromethane, to the solution is added 2.2 mL (13.9 mmol) of triethylsilane and 4.3 mL (55.7 mmol) of trifluoroacetic acid. The reaction is stirred at rt overnight and then quenched with water and neutralized with solid sodium bicarbonate. The organic layer is washed with water followed by brine. The organic phase is dried over sodium sulfate and the solvent removed under reduced pressure. Flash chromatography using a 1:1 mixture of ethyl acetate and hexane affords 0.42 g (1.55 mmol) of 5-(thiophen-2-ylmethyl)imidazole-1-sulfonic acid dimethylamide (5). (5) (0.42 g, 1.55 mmol) is taken up in 10 mL of a 1.5N HCl solution and heated at reflux for 3 h and then stirred at rt overnight. The reaction is diluted with ethyl acetate, neutralized with solid sodium bicarbonate and then made basic with 2N NaOH. The organic layer is washed with water followed by brine. The organic phase is dried over sodium sulfate and the solvent removed under reduced pressure. Flash chromatography using a 10:1 mixture of chloroform and methanol affords 0.17 g (1.0 mmol) of 4(5)-thiophen-3-ylmethyl-1H-imidazole (6) (C-1).

1. customThe next day the reaction is quenched with water
2. extractionextracted with ethyl acetate
3. washThe organic layer is washed with water
4. dry with materialThe organic phase is dried over sodium sulfate
5. customthe solvent removed under reduced pressure
6. stirringThe reaction is stirred at rt overnight
7. customquenched with water and neutralized with solid sodium bicarbonate
8. washThe organic layer is washed with water
9. dry with materialThe organic phase is dried over sodium sulfate
10. customthe solvent removed under reduced pressure
11. additiona 1:1 mixture of ethyl acetate and hexane

ORD record

ord-6a1518ca2c694e7c850204ccd98e8f1a

Source dataset

uspto-grants-2001_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06329369B1