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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylpiperidin-4-amine | HCID 417391 | — |
| Reactant | HCID 59548940 | HCID 59548940 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 49783679 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399456B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-cd98d00b82cb466a8139d9fb9e42425a |
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| Source note | uspto-grants-2013_03 |
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