HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloride methanol → N-{4-[(1R)-1-aminoethyl]-2-methylphenyl)methanesulfonamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | N-[4-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-methylphenyl]methanesulfonamide | HCID 58640404 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-{4-[(1R)-1-aminoethyl]-2-methylphenyl)methanesulfonamide hydrochloride | HCID 21097519 | — |
Reaction Steps
To N-[4-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-methylphenyl]methanesulfonamide (530 mg, 1.60 mmol) was added HCl-methanol (2.0 M, 5.0 mL) and 1,4-dioxane (5.0 mL). The solution was stirred at room temperature for 30 minutes and then concentrated in vacuo. Diethyl ether was added to precipitate amine hydrochloride. The precipitate was then filtered and washed with diethyl ether (450 mg, quant) to furnish 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-a0458d0345a94e5f8c4dcca15465382a |
| Source note | uspto-grants-2009_07 |