HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855896Generated: October 28, 2026
Diisopropylethylamine → 4-Amino-1-(5-methanesulfonyl-2-pyridyl)-4-methylpiperidine
https://huagongshe.com/reaction/855896
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Bromo-5-(methylsulfonyl)pyridine | HCID 9899483 | — |
| Reactant | Benzyl (4-methylpiperidin-4-yl)carbamate hydrochloride | HCID 24728615 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Amino-1-(5-methanesulfonyl-2-pyridyl)-4-methylpiperidine | HCID 17860982 | 72.6% |
Reaction Steps
A solution of (4-methyl-piperidin-4-yl)-carbamic acid benzyl ester hydrochloride salt (0.37 g, 1.3 mmol, Example 30B), 2-bromo-5-(methylsulfonyl)pyridine (0.27 g, 1.15 mmol) and diisopropylethylamine (0.7 mL) in dioxane (4 mL) in a sealed tube was heated to 80° C. for 16 hours. The mixture was cooled, concentrated under reduced pressure and purified by chromatography (silica gel, eluting with 5% hexane/ethyl acetate to 25% ethyl acetate/hexane) to provide the titled compound (0.225 g) as a white solid. MS (CI) m/z 404 (M+1)+; 1H NMR (300 MHz, CDCl3) δ ppm 8.63 (d, 1H), 7.86 (dd, 1H), 7.37 (m, 5H), 6.65 (d, 1H), 5.07 (s, 2H), 4.67 (s, 1H), 4.04-3.96 (m, 2H), 3.49-3.39 (m, 2H), 3.03 (s, 3H), 2.19-2.12 (m, 2H), 1.71-1.61 (m, 2H), 1.41 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262207B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-c7554e71a24342759a327a3e1620561c |
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| Source note | uspto-grants-2007_08 |
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