HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432426Generated: November 3, 2026
Methanesulfonyl chloride → HCID 11704573, compound
https://huagongshe.com/reaction/1432426
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 10345947 | HCID 10345947 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11704573 | HCID 11704573 | 28.1% |
Reaction Steps
Methanesulfonyl chloride (0.009 mL, 0.12 mmol) and diisopropylethylamine (0.026 mL, 0.15 mmol) were added to a solution of 2-(5-benzo[1,3]dioxol-5-yl-2-piperidin-4-yl-3H-imidazol-4-yl)-pyridine (0.035 g, 0.10 mmol; prepared as described in Example 11) in anhydrous THF (3 mL). The reaction mixture was stirred at room temperature for 3 hours. Solvent was removed under reduced pressure, and the residue was dissolved in 1 mL DMSO. The DMSO solution was filtered and injected onto preparative HPLC. HPLC purification eluting with acetonitrile:water gave 0.012 g (28%) of the title compound as a yellow solid. MS (ESP+) m/z 427.1 (M+1). 1H NMR (400 MHz, CDCl3) δ 8.65 (m, 1H), 7.83 (m, 1H), 7.56 (m, 1H), 7.45 (m. 1H), 7.03 (dd, 1H, J=1.8 Hz, 8.1 Hz), 6.97 (d, 1H, J=1.8 Hz), 6.88 (d, 1H, d=8.1 Hz), 6.05 (s, 2H), 3.91 (m, 2H), 3.47 (m, 1H), 2.89 (m, 2H), 2.84 (s, 3H), 2.22 (m, 2H), 2.11 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612094B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-862cbc4a96c74eeb88498d76728788c8 |
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| Source note | uspto-grants-2009_11 |
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