HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Piperidinecarboxylic acid → 2-(piperidin-4-yl)-1H-1,3-benzodiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Piperidinecarboxylic acid | HCID 3773 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 2-(piperidin-4-yl)-1H-1,3-benzodiazole | HCID 715810 | 38% |
Reaction Steps
This compound is synthesized as described by adaptation of the following reference: J. Heterocyclic Chem., 1989, 26, 54. A mixture of benzene-1,2-diamine (12.6 g, 116 mmol), piperidine-4-carboxylic acid (15 g, 116 mmol) and 4M aqueous HCl (250 mL) is stirred and heated under reflux for 48 h. The reaction mixture is cooled to room temperature and is made basic by addition of 5M aqueous NaOH. The precipitate formed is collected by suction filtration, washed with water and dried in the vacuum oven to afford 8.8 g (38%) of 2-(piperidin-4-yl)-1H-benzimidazole. m/z=202 [M++H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609696B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-928d8aeccbed413496fc2d1e4e3f0f88 |
| Source note | uspto-grants-2013_12 |