HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → HCID 86724103, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 3-(6-Bromopyridin-2-yl)-3-oxopropanenitrile | HCID 53417229 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86724103 | HCID 86724103 | 81.6% |
Reaction Steps
To a solution of 3-(6-bromo-2-pyridyl)-3-oxo-propanenitrile (1.71 g, 7.6 mmol, Preparation A.1) in ethanol (50 mL) was added methyl hydrazine (1.20 mL, 22.8 mmol). The resulting mixture was stirred for about 30 min at rt and then heated under reflux for about 4 h. After cooling to rt the reaction mixture was concentrated in vacuo. The residue was purified by column chromatography (SiO2, ethyl acetate/hexanes 1:2) to give 3-(6-bromo-2-pyridyl)-2-methyl-pyrazol-5-amine (1.56 g, 6.2 mmol, 81%) as an off white solid: 1H-NMR (CDCl3, Bruker 400 MHz) δ 3.57 (2 H, br s); 3.75 (3 H, s); 5.90 (1 H, s); 7.34 (1 H, d, J=8 Hz); 7.52 (1 H, t, J=8 Hz); 7.82 (1 H, d, J=8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150592B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-0cb92ebb57f04cf6a45ae4546b535f65 |
| Source note | uspto-grants-2015_10 |