HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → (4-chloro-2-methyl-5-pyridin-3-yl-2H-pyrazol-3-yl)-methylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | methyl-(2-methyl-5-pyridin-3-yl-2H-pyrazol-3-yl)-amine | HCID 67499915 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (4-chloro-2-methyl-5-pyridin-3-yl-2H-pyrazol-3-yl)-methylamine | HCID 67499720 | 24% |
Reaction Steps
A mixture of methyl-(2-methyl-5-pyridin-3-yl-2H-pyrazol-3-yl)-amine (0.35 g, 1.8 mmol) and N-chlorosuccinimide (0.273 g, 2 mmol) was combined in acetonitrile (3 mL), stirred at room temperature for 30 minutes, concentrated under reduced pressure and purified using silica gel chromatography eluting with a gradient of EtOAc in hexanes to yield the title compound as a yellow oil (0.096 g, 23%): IR (thin film) 1581.6 cm−1; 1H NMR (400 MHz, CDCl3) δ 9.12 (d, J=1.5 Hz, 1H), 8.57 (dd, J=4.8, 1.3 Hz, 1H), 8.15 (ddd, J=7.8, 2.0, 2.0 Hz, 1H), 7.33 (dd, J=8.1, 5.1 Hz, 1H), 3.80 (s, 3H), 2.91 (d, J=5.8 Hz, 3H); ESIMS (m/z) 225.6 [M+2].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09422278B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-52badb314c3a449f8d89584860051fca |
| Source note | uspto-grants-2016_08 |