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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946839Generated: October 30, 2026

N,N-Dimethylpiperidin-4-amine → HCID 49783679, compound

https://huagongshe.com/reaction/1946839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Dimethylpiperidin-4-amineHCID 417391—
ReactantHCID 59548940HCID 59548940—
SolventDichloromethaneHCID 6344—
ProductHCID 49783679HCID 49783679—

Reaction Steps

To a solution of compound 26 (0.200 g, 0.59 mmol) in DCM was added TEA (0.090 g, 0.89 mmol) and 4-dimethylaminopiperidine (0.114 g, 0.89 mmol). The reaction was monitored by HPLC. The reaction was complete after stirring at room temperature for 16 hrs. DCM was removed in vacuo, and the resulting solid was dissolved in a minimal amount of DCM and purified with chromatography with a gradient of 10 to 30% MeOH in DCM. Pure fractions were combined and evaporated in vacuo to yield an oil, which was triturated with DCM and hexanes, and then filtered to yield compound 72 as a peach solid (0.124 g, 49% yield). HPLC purity: 96.5%; 1H NMR (500 MHz, DMSO-d6): δ 8.22 (d, J=2 Hz, 1H), 7.84 (dd, J1=2 Hz, J2=8 Hz, 1H), 7.41 (d, J=6 Hz, 1H), 7.39 (s, 1H), 7.34 (d, J=8 Hz, 1H), 6.70 (d, J=8 Hz, 1H), 3.8 (d, J=13 Hz, 2H), 2.84 (t, J=12 Hz, 2H), 2.31 (s, 3H), 2.26 (m, 1H), 2.25 (s, 3H), 2.15 (s, 6H), 1.79 (d, J=12 Hz, 2H), 1.43 (m, 2H); MS (ESI, EI+): m/z=430 (MH+); melting point: 136-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399456B2
Source datasetuspto-grants-2013_03
ORD IDord-cd98d00b82cb466a8139d9fb9e42425a
Source noteuspto-grants-2013_03