HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)pyridine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 6-(1-(tert-butoxycarbonyl)piperidin-4-yl)nicotinate | HCID 86730350 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)pyridine-3-carboxylic acid | HCID 86730349 | 52% |
Reaction Steps
A 2 M sodium hydroxide solution (20 mL) was added to a solution of methyl 6-(1-(tert-butoxycarbonyl)piperidin-4-yl)nicotinate described in Production Example 28-2 (1.07 g, 3.32 mmol) in ethanol (5 mL), and the mixture was stirred for 1 hour. 2 M hydrochloric acid was added to the reaction liquid at 0° C. The aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with a saturated saline solution and then dried over anhydrous sodium sulfate. The drying agent was separated by filtration and then the filtrate was concentrated under vacuum to obtain the title compound (534 mg, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08933099B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-4f2dfd6fb92c4eea90ae5c4f177f9485 |
| Source note | uspto-grants-2015_01 |