HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid monohydrate → 2-amino-3-methyl-N-(2-morpholinoethyl)-pentanamide Ditosylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2-amino-3-methyl-N-[2-(morpholin-4-yl)ethyl]pentanamide | HCID 11959372 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-amino-3-methyl-N-(2-morpholinoethyl)-pentanamide Ditosylate | HCID 86675481 | 90% |
Reaction Steps
To a solution of 2-amino-3-methyl-N-(2-morpholinoethyl)-pentanamide free base (15 g, 0.062 mol) dissolved in anhydrous tetrahydrofuran (300 mL, 20 vol) was added p-toluenesulfonic acid monohydrate (23.4 g, 0.123 mol, 2 eq) in one portion. The initially clear mixture becomes cloudy and produces a mild exotherm. After about 15 min, crystals begin to precipitate from solution and the mixture continued to stir for 1.5 h. The solids were collected by vacuum filtration, and the wet cake was dried in a 40° C. vacuum oven to afford 32.5 g (90% yield) of 2-amino-3-methyl-N-(2-morpholinoethyl)-pentanamide Ditosylate as a white solid. 1H NMR confirmed the identity and XRD pattern matches the small scale screen sample pattern.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09271986B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-d5c6438016eb415aa820d5c3f6964a6f |
| Source note | uspto-grants-2016_03 |