HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → {4-[(2-Pyridin-3-ylpiperidin-1-yl)sulfonyl]phenyl}amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(4-{[2-(pyridin-3-yl)piperidin-1-yl]sulfonyl}phenyl)acetamide | HCID 659759 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | {4-[(2-Pyridin-3-ylpiperidin-1-yl)sulfonyl]phenyl}amine | HCID 2770922 | 78.7% |
Reaction Steps
A 1.81 ml portion of methanesulfonic acid was added to a methanol solution (10 ml) of 1.0 g N-(4-{[2-(pyridin-3-yl)piperidin-1-yl]sulfonyl}phenyl)acetamide and stirred overnight at room temperature. The reaction liquid was poured into ice water and neutralized with sodium bicarbonate, and then layer separation operation was carried out by adding ethyl acetate. The organic layer was washed with saturated sodium chloride aqueous solution, dried with anhydrous sodium sulfate and then concentrated under a reduced pressure to obtain 695 mg of 4-{[2-(pyridin-3-yl)piperidin-1-yl]sulfonyl}aniline as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101580B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-4b59a8b4d78b455c86b6d0f266d83bd8 |
| Source note | uspto-grants-2012_01 |