HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 66591622, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| Reactant | HCID 66591684 | HCID 66591684 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 66591622 | HCID 66591622 | 73.9% |
Reaction Steps
A mixture of 4-(4-{2-oxo-2-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethylcarbamoyl}-[1,2,3]triazol-1-yl)-piperidine-1-carboxylic acid tert-butyl ester (prepared by the method used for the synthesis of Example 136, starting from 1-Boc-4-aminopiperidine) (380 mg, 0.65 mmol) in dioxane.HCl (5 mL) was stirred at ambient temperature for 1 hr. The reaction mixture was concentrated under reduced pressure to get the crude solid which was purified by recrystallisation from a mixture of MeOH and diethyl ether to afford 252 mg (73.9% Yield) of 1-piperidin-4-yl-1H-[1,2,3]triazole-4-carboxylic acid {2-oxo-2-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethyl}-amide hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129376B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-9b764e143f5d429cb468d56458bc4aa6 |
| Source note | uspto-grants-2012_03 |