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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264270Generated: October 30, 2026

1-(4-Aminopiperidin-1-yl)ethan-1-one → HCID 58692219, compound

https://huagongshe.com/reaction/2264270

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Aminopiperidin-1-yl)ethan-1-oneHCID 4962477—
ReactantHCID 59596028HCID 59596028—
ProductHCID 58692219HCID 5869221912.1%

Reaction Steps

Using the procedure of example 1, 1-(4-aminopiperidin-1-yl)ethanone (350 mg) was reacted with compound 1f (300 mg) to provide compound 64 (33 mg, 12%). 1H NMR (300 MHz, CDCl3) δ 11.45 (s, 1 H), 8.75 (d, 1 H), 8.40 (d, 1 H), 8.20 (d, 1 H), 8.12 (s, 1 H), 8.00 (s, 1 H), 7.20 (m, 1H), 6.90 (d, 1 H), 5.40 (m, 1 H) (rotamer), 4.55 (m, 1 H), 4.20-3.70 (m, 2 H), 3.40-2.70 (m, 2 H), 2.20 (m, 2 H), 2.15 (s, 3 H), 1.50 (m, 2H). MS (ESI) m/z: 337 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855205B2
Source datasetuspto-grants-2010_12
ORD IDord-b94b50563ba14e598680051103466b5c
Source noteuspto-grants-2010_12