HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl((1-methylpiperidin-3-yl)methyl)amine → HCID 178426430, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl((1-methylpiperidin-3-yl)methyl)amine | HCID 16640588 | — |
| Reactant | HCID 178426451 | HCID 178426451 | — |
| Product | HCID 178426430 | HCID 178426430 | — |
Reaction Steps
The title compound was prepared in a manner similar to Example 112 using 6-(4-(4-cyano-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and N-methyl-1-(1-methylpiperidin-3-yl)methanamine. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.09-1.27 (m, 1H) 1.45-1.92 (m, 3 H) 2.15 (br. s., 2 H) 2.37-2.47 (m, 4 H) 2.57-2.75 (m, 3 H) 2.96 (s, 4H) 3.28 (dd, J=12.88, 5.81 Hz, 3 H) 3.49 (d, J=15.41 Hz, 1 H) 7.47 (d, J=8.53 Hz, 1 H) 7.52 (s, 1 H) 7.84 (s, 1 H) 7.89 (br. s., 1 H) 8.20 (d, J=8.34 Hz, 1 H) 8.49 (br. s., 1 H) 8.52 (d, J=8.84 Hz, 1 H); ESI-MS m/z [M+H]+ 445.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040522B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-9a45e7b170af4e70879ce77f74310741 |
| Source note | uspto-grants-2015_05 |