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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant5-(Tetrahydro-pyran-4-yl)-thiophene-3-carboxylic acidHCID 59542592—
SolventDimethylformamideHCID 6228—
ProductPiperidin-1-yl-[5-(tetrahydro-pyran-4-yl)-thiophen-3-yl]-methanoneHCID 4264435453%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362008B2
Source datasetuspto-grants-2013_01
ORD IDord-a4ce60e552c6469da1cc457b658d1163
Source noteuspto-grants-2013_01