Water → HCID 67260844, compound

3-(4-bromo-2-thienyl)-1H-pyrazole (8.7 mmol) was dissolved in 20 mL dry N,N-dimethylformamide under argon atmosphere. Sodium hydride (10.5 mmol, 60% dispersion in mineral oil) was added in portions at room temperature. The reaction mixture was stirred at room temperature for 15 min. Isopropyl iodide (13.1 mmol) was added dropwise and the reaction mixture was stirred at room temperature for 14 h. Water and MTBE were added to the reaction mixture. The phases were separated and the aqueous phase was extracted with MTBE. The combined organic extracts were successively washed with water and brine, dried over MgSO4, filtered and concentrated. The residue was purified by chromatography on silica gel (cyclohexane:ethyl acetate 100:0 to 0:100) to afford 1.90 g 3-(4-bromo-2-thienyl)-1-isopropyl-1H-pyrazole (71% yield). Traces of the minor regioisomer 5-(4-bromo-2-thienyl)-1-isopropyl-1H-pyrazole were collected and analyzed as well.

1. stirringthe reaction mixture was stirred at room temperature for 14 h
2. customThe phases were separated
3. extractionthe aqueous phase was extracted with MTBE
4. washThe combined organic extracts were successively washed with water and brine
5. dry with materialdried over MgSO4
6. filtrationfiltered
7. concentrationconcentrated
8. customThe residue was purified by chromatography on silica gel (cyclohexane:ethyl acetate 100:0 to 0:100)

ORD record

ord-788fde26cd5140cfb9fe281eb8ee63d9

Source dataset

uspto-grants-2014_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08685974B2