HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 86643500, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-Chloro-3-pyridylamine | HCID 80528 | — |
| Reactant | Toluene water | HCID 22272177 | — |
| Reactant | HCID 68430510 | HCID 68430510 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 86643500 | HCID 86643500 | 49.8% |
Reaction Steps
A mixture of p-toluenesulfonic acid (10 mg), 2-(4-Fluoro-phenyl)-1-(2-methylthio-pyrimidin-4-yl)-ethanone (200 mg, 0.76 mmoles) and 3-amino-2-chloropyridine (90 mg, 0.7 mmoles) in 3 mL of toluene was refluxed overnight with a Dean-Stark removal of water/toluene azeotrope. The reaction mixture was further concentrated, the brown residue suspended in an ethyl acetate/hexane mixture (9/1) and filtered. The solid was solubilised in ethyl acetate and purified by chromatography on silica gel (ethylacetate/hexane 1/1) to give 130 mg of (2-Chloro-pyridin-3-yl)-[2-(4-fluoro-phenyl)-1-(2-methylthio-pyrimidin-4-yl)-ethylidene]-amine as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084395B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-a07094c3b3514f33a195038242b7295b |
| Source note | uspto-grants-2011_12 |