HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655028Generated: October 30, 2026
Dimethylformamide → HCID 15117093, compound
https://huagongshe.com/reaction/655028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19887050 | HCID 19887050 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15117093 | HCID 15117093 | 91.3% |
Reaction Steps
A stirred mixture of 4.0 g of 3-(1-piperazinyl)-1-[4-(trifluoromethyl)phenyl]-1H-indazole hydrochloride, 2.4 g of (2-bromoethyl)benzene, 1.8 g of potassium carbonate and 60 ml of dimethylformamide was heated, under nitrogen, at 70°-75° for 8 hours, and then stirred at ambient temperature for 8 hours. The reaction mixture was poured into water, and the aqueous mixture extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate and concentrated to an oil. The oil was chromatographed on a Water's Model High Pressure Liquid Chromatograph utilizing silica columns and eluting with hexane/ethyl acetate (30%). Concentration of the appropriate fractions gave 4.3 g of 3-[4-(2-phenylethyl)-1-piperazinyl]-1-[4-(trifluoromethyl)phenyl]-1H-indazole. The free base was dissolved in diethyl ether and treated with hydrogen chloride to precipitate the corresponding hydrochloride salt. Recrystallization from ethanol/diethyl ether gave 3.1 g of 3-[4-(2-phenylethyl)-1-piperazinyl]-1-[ 4-(trifluoromethyl) phenyl]-1H-indazole hydrochloride, mp 255°-257°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05134236 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-3f03c5e7ce094909a1108648d804cd3d |
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| Source note | uspto-grants-1992_07 |
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