Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239407Generated: October 29, 2026

1-(4-Aminopiperidin-1-yl)ethan-1-one → HCID 57989856, compound

https://huagongshe.com/reaction/239407

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Aminopiperidin-1-yl)ethan-1-oneHCID 4962477—
ReactantHCID 86636585HCID 86636585—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57989856HCID 57989856—

Reaction Steps

Following a procedure analogous to the procedure described in Example 1 using N-{5-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,5-difluorobenzenesulfonamide (0.10 g, 0.19 mmol) and 1-acetyl-4-piperidinamine (0.27 g, 1.9 mmol) in THF (1 mL) the title compound was obtained as an off-white solid (0.075 g, 0.12 mmol, 62% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 10.82 (s, 1H), 8.12 (d, J=5.0 Hz, 1H), 7.68-7.43 (m, 3H), 7.44-7.17 (m, 5H), 4.33-4.18 (m, 1H), 3.83-3.73 (m, 1H), 3.44-3.20 (m, 2H), 2.66-2.32 (m, 4H), 1.99 (s, 3H), 1.36 (d, J=6.8 Hz, 6H), 1.35-1.10 (m, 2H). MS (ESI): 631 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642759B2
Source datasetuspto-grants-2014_02
ORD IDord-e0f5699777a54267bb68d920d0cd7c85
Source noteuspto-grants-2014_02