HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878390Generated: November 2, 2026
Sodium Iodide → N-tert-Butyl-3-((4-(3-fluoro-4-nitrobenzoyl)-2-(fluoromethyl)piperazin-1-yl)methyl)benzamide
https://huagongshe.com/reaction/1878390
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-tert-butyl-3-(chloromethyl)benzamide | HCID 43156221 | — |
| Reactant | (3-Fluoro-4-nitrophenyl)(3-(fluoromethyl)piperazin-1-yl)methanone | HCID 66878536 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-tert-Butyl-3-((4-(3-fluoro-4-nitrobenzoyl)-2-(fluoromethyl)piperazin-1-yl)methyl)benzamide | HCID 57917722 | 57.3% |
Reaction Steps
A stirred mixture of (3-fluoro-4-nitrophenyl)(3-(fluoromethyl)piperazin-1-yl)methanone (456 mg, 1.6 mmol), N-tert-butyl-3-(chloromethyl)benzamide (361 mg, 1.6 mmol), triethylamine (3.1 mmol, 341 mg) and sodium iodide (1.6 mmol, 240 mg) in acetonitrile (10 mL) was heated to 60° C. for several hours. The reaction was concentrated under reduced pressure. The residue was then dissolved in dichloromethane and extracted with water (×3). The organic phase was dried (sodium sulfate) and concentrated under vacuum. The crude material was purified using silica chromatography to give the title compound (435 mg). MS (ESI) m/z 475.7[M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314091B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-736fb81fe7f04add9513906cdd091f46 |
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| Source note | uspto-grants-2012_11 |
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