HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-(Piperidin-4-yl)-1,3-benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(4-(Benzo[d]thiazol-2-yl)piperidin-1-yl)ethanone | HCID 9218695 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Piperidin-4-yl)-1,3-benzothiazole | HCID 1477439 | 46% |
Reaction Steps
To a solution of 1.4 g of 1-(4-(benzothiazol-2-yl)piperidin-1-yl)ethanone in 10 mL of MeOH was added 7.5 mL of KOH (45 wt. % solution). After refluxing for 18 hours, the reaction was cooled to room temperature. The mixture was partitioned between EtOAc and water. The organic phase was washed with brine and dried over MgSO4. Concentration under reduced pressure gave 540 mg of the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248755B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-d0be67bac92b4883aa6f514c01c77427 |
| Source note | uspto-grants-2001_06 |