HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700598Generated: November 2, 2026
Methanesulfonic Acid → HCID 178493040, compound
https://huagongshe.com/reaction/1700598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 10913183 | HCID 10913183 | — |
| Reactant | HCID 178418668 | HCID 178418668 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178493040 | HCID 178493040 | 103.6% |
Reaction Steps
To a solution of aminoguanidine hydrochloride (0.048 g) in methanol (20 ml) was added methanesulfonic acid (0.042 g), and the mixture was refluxed for 1 hour. To the mixture were added 7-(2-chlorophenyl)-4-methoxy-5,6,7,8-tetrahydroquinolin-5-one (0.12 g) and methanesulfonic acid (0.042 g), and the mixture was stirred at 50° C. for 9 hours and at 60° C. for 16 hours. Under reduced pressure, the solvent was evaporated. To the residue was added water, and the mixture was washed with ethyl acetate. Under reduced pressure, the solvent was evaporated, and the residue was recrystallized from water-ethanol to give 7-(2-chlorophenyl)-5-guanidinoimino-4-methoxy-5,6,7,8-tetrahydroquinoline methanesulfonate (Compound 79) (0.19 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06350749B1 |
|---|
| Source dataset | uspto-grants-2002_02 |
|---|
| ORD ID | ord-7569e7388a9543f0b1e84c0758386150 |
|---|
| Source note | uspto-grants-2002_02 |
|---|