HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256345Generated: October 30, 2026
2-(4-Piperidyl)-2-propanol → HCID 67064559, compound
https://huagongshe.com/reaction/1256345
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(4-Piperidyl)-2-propanol | HCID 5200321 | — |
| Reactant | N-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide | HCID 86652267 | — |
| Catalyst | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67064559 | HCID 67064559 | 41% |
Reaction Steps
A solution of N-(7-chloro-pyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide (2D, 200 mg, 0.604 mmol) and 2-(piperidin-4-yl)propan-2-ol (130 mg, 0.906 mmol) in Dioxane (6 mL) was stirred at 85° C. overnight. After cooling to room temperature, the mixture was diluted with a few drops of DMSO and methanol, and was then purified by preparatory HPLC, 5-95% (MeCN/H2O gradient+0.01% TFA). Lyophilization of the combined fractions gave the titled compound as a white solid (105 mg, 41%). 1H NMR (METHANOL-d4) δ: 8.00 (d, J=2.3 Hz, 1H), 7.95 (d, 2H), 7.66 (d, J=8.3 Hz, 2H), 7.39 (s, 1H), 6.33 (d, J=1.5 Hz, 1H), 4.59 (d, J=11.6 Hz, 2H), 2.97 (t, 2H), 1.95 (d, J=9.1 Hz, 2H), 1.61-1.69 (m, 3H), 1.56 (s, 6H), 1.21 (s, 6H). ESI-MS: m/z 438.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461163B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-fcdd2d3df89f42788734f3d1cef1dc3a |
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| Source note | uspto-grants-2013_06 |
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