HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → Nanterinone mesylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Nanterinone | HCID 71305 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Nanterinone mesylate | HCID 92089 | — |
Reaction Steps
A stirred solution of 8-methyl-6-(2,4-dimethylimidazol-1-yl)-2-(1H)-quinolone (365.7 g) in methanol (914 cm3) at 60° was treated with methanesulphonic acid (141.9 g) over 5 minutes. Ethyl acetate (3.4 l) was added and the solution was allowed to cool to room temperature for 1 hour followed by cooling in an ice bath for 2 hours. The solid was filtered off, washed with ethyl acetate (450 cm3) and dried in vacuo at 50° to afford the title compound, m.p. 282°-284°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04728653 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-50ff35339abf4d62bb5039949dc743ec |
| Source note | uspto-grants-1988_03 |