HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-((5-bromo-2-chloropyridin-4-yl)methylene)-2-methylpropan-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 5-Bromo-2-chloropyridine-4-carbaldehyde | HCID 53418381 | — |
| Product | N-((5-bromo-2-chloropyridin-4-yl)methylene)-2-methylpropan-2-amine | HCID 86674941 | 107.1% |
Reaction Steps
To a mixture of 5-bromo-2-chloroisonicotinaldehyde (1.047 g, 4.749 mmol) and Water (2.0 mL, 110 mmol) was added tert-butylamine (2.0 mL, 19 mmol). The reaction mixture was stirred at room temperature for 20 hours, and then excess tert-butylamine was removed by rotary evaporation. The resulting residue was partitioned between ethyl acetate and water, and the organic layer dried with brine and MgSO4, filtered, and evaporated in vacuo to yield 1.401 g (87%) of N-((5-bromo-2-chloropyridin-4-yl)methylene)-2-methylpropan-2-amine. 1H NMR (400 MHz, DMSO) δ 8.72 (s, 1H), 8.43 (s, 1H), 7.78 (s, 1H), 1.28 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09206175B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-85412a6799804f5193757dbc0100e076 |
| Source note | uspto-grants-2015_12 |