HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730703Generated: October 25, 2026
Dimethyl Sulfoxide → 2-Piperazin-1-yl-6-trifluoromethyl-1H-benzoimidazole
https://huagongshe.com/reaction/730703
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-chloro-6-(trifluoromethyl)-1H-benzimidazole | HCID 337905 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Piperazin-1-yl-6-trifluoromethyl-1H-benzoimidazole | HCID 11666201 | — |
Reaction Steps
A mixture of 2-chloro-6-trifluoromethyl-1H-benzoimidazole (221 mg, 1 mmol, Example 1c), piperazine (172 mg, 2 mmol, Aldrich) and DMSO (2 mL) was stirred at 80° C. for 24 h. The mixture was cooled to room temperature, water (10 mL) was added and the mixture was extracted with EtOAc (2×20 mL). The combined organic phases were washed with water (2×5 mL) and brine (5 mL), dried over Na2SO4, and filtered. The solvent was removed in vacuo and the residue was purified by silica gel chromatography, eluting with 10% MeOH/CH2Cl2+1% ammonia (30% in water) to give the title compound. MS (ESI, pos. ion) m/z: 271 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582761B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-e86feb2cc7564c5fb9120f920da27bee |
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| Source note | uspto-grants-2009_09 |
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