HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689845Generated: November 1, 2026
1-Pentanesulfonyl chloride → HCID 11386162, compound
https://huagongshe.com/reaction/1689845
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Pentanesulfonyl chloride | HCID 237555 | — |
| Reactant | HCID 66905728 | HCID 66905728 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11386162 | HCID 11386162 | 4% |
Reaction Steps
1-Pentanesulfonyl chloride (0.034 g, 0.30 mmol) was added slowly to a solution of [4-(5-aminopyridin-2-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)methanone in pyridine (2 mL) at 0° C. The mixture was stirred at 25° C. for 16 hours and then diluted with dichloromethane. The organic phase was washed with water and saturated NaCl solution, dried over anhydrous MgSO4. After removal of dichloromethane, the product was purified by column chromatography to afford the title compound in 4% yield (2.7 mg). 1H NMR (300 MHz, CDCl3) δ 8.02, 7.87, 7.74, 7.61, 7.36, 6.94, 4.47, 4.11, 3.87, 3.68, 3.60, 3.42, 2.99, 1.77, 1.32, 0.88. MS (ES+) m/z 485.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153636B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-ef664399341d44b5a0c1e74083654245 |
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| Source note | uspto-grants-2012_04 |
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