HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-3-pyridylamine → HCID 73088680, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-3-pyridylamine | HCID 80528 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2-(4-Fluorophenyl)-1-(pyridin-4-yl)ethanone | HCID 11042133 | — |
| Reactant | Toluene water | HCID 22272177 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 73088680 | HCID 73088680 | 64% |
Reaction Steps
To a solution of 2-(4-fluorophenyl)-1-(pyridin-4-yl)ethanone (5.20 g, 24 mmol) and 3-amino-2-chloropyridine (4.04 g, 31.4 mmol) in toluene (150 ml) was added p-toluenesulfonic acid monohydrate (457 mg. 2.4 mmol) and the reaction mixture was brought to reflux with Dean-Stark removal of the toluene/water azeotrope. After 24 h, toluene was removed in vacuo and the residue was resuspended in ethyl acetate. The precipitate was collected by vacuum filtration to give (2-chloropyridin-3-yl)-[2-(4-fluorophenyl)-1-(pyridin-4-yl)-vinyl]amine (5.0 g) as a tan solid. The filtrate was concentrated in vacuo and purified by flash column chromatography (50%-80% ethyl acetate:hexanes gradient) to give additional 1.50 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06479507B2 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-e999f75cd32948e89c6e5319467ceca4 |
| Source note | uspto-grants-2002_11 |