HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809050Generated: October 30, 2026
Piperidine → Piperidin-1-yl-[5-(tetrahydro-pyran-4-yl)-thiophen-3-yl]-methanone
https://huagongshe.com/reaction/1809050
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 5-(Tetrahydro-pyran-4-yl)-thiophene-3-carboxylic acid | HCID 59542592 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Piperidin-1-yl-[5-(tetrahydro-pyran-4-yl)-thiophen-3-yl]-methanone | HCID 42644354 | 53% |
Reaction Steps
5-(Tetrahydro-pyran-4-yl)-thiophene-3-carboxylic acid (0.107 g, 0.5 mmol) was dissolved in DMF (2 mL). DIPEA (1.0 mmol), HATU (0.5 mmol) and piperidine (0.5 mmol) were added and the reaction stirred at room temperature for 1 hour. The reaction was then partitioned between ethyl acetate and water and the organic solution separated and dried over magnesium sulphate, filtered and the solvent evaporated. The product was purified by HPLC, eluting with 40%-90% acetonitrile in water (0.1% formic acid) over 30 minutes. The fractions containing the desired product were concentrated under vacuum to give the title compound (74 mg). LCMS m/z 280.22 [M+H]+ RT=8.77 min (Analytical Method 1). 1H NMR δ (ppm)(CHCl3-d): 7.25 (s, 1H), 6.9 (t, 1H), 4.1-4.0 (m, 2H), 3.6 (m, 4H), 3.5 (m, 2H), 3.1-3.0 (m, 1H), 1.95-1.6 (m, 10H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362008B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-a4ce60e552c6469da1cc457b658d1163 |
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| Source note | uspto-grants-2013_01 |
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