HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloride methanol → ethyl 5-[(1R)-1-aminoethyl]-2-[(methylsulfonyl)amino]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | Ethyl5-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-[(methylsulfonyl)amino]benzoate | HCID 57762930 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | ethyl 5-[(1R)-1-aminoethyl]-2-[(methylsulfonyl)amino]benzoate | HCID 57762927 | 98.4% |
Reaction Steps
To a solution of ethyl 5-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-[(methylsulfonyl)amino]benzoate (4.3 g,11 mmol) in methanol (30 ml) was added hydrogenchloride-methanol solution (30 ml). The solution was stirred at room temperature for 30 minutes and then concentrated under reduced pressure. The given residue was recrystallized from methanol-diethyl ether. The precipitate was then filtered, washed with diethyl ether and collected to furnish 3.1 g (87% yield) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566739B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-03cf9079803349db97cb6c5dd4de1683 |
| Source note | uspto-grants-2009_07 |