HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 5-Methanesulphonamido-2-[N-(6-methanesulphonamidoquinol-2-ylmethyl)-N-methylamino]indane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Chloromethyl-6-methanesulphonamidoquinoline | HCID 19045572 | — |
| Reactant | 5-Methanesulphonamido-2-methylaminoindane | HCID 19888659 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Methanesulphonamido-2-[N-(6-methanesulphonamidoquinol-2-ylmethyl)-N-methylamino]indane | HCID 19888658 | — |
Reaction Steps
5-Methanesulphonamido-2-methylaminoindane (0.09 g), 2-chloromethyl-6-methanesulphonamidoquinoline (0.1 g) and sodium bicarbonate (0.2 g) were heated under reflux in acetonitrile (10 ml) for 11/2 hours. The solvent was then removed by evaporation in vacuo and the residue was taken up in methylene chloride, washed with aqueous sodium bicarbonate, dried (MgSO4) and evaporated in vacuo. The residue was purified by column chromatography on silica eluting with methylene chloride containing methanol (0% up to 2%) and the product-containing fractions were combined and evaporated to give the title compound as a form, yield 0.09 g. A sample was crystallised from deuterochloroform, m.p. 189°-191°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04829071 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-d497b3443726499eb3e9e06a9d99cd9f |
| Source note | uspto-grants-1989_05 |