Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86758141 | HCID 86758141 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86758140 | HCID 86758140 | 69.5% |
Reaction Steps
0.3 g of (prop-2-ynyl) (3R,4R)-4-[3-(6-methoxyquinolin-4-yl)propyl]-1-(prop-2-ynyl)piperidine-3-carboxylate in 3 cm3 of dioxane and 1.48 cm3 of N sodium hydroxide were heated, with stirring, at a temperature in the region of 70° C. for 17 hours. The reaction mixture was concentrated under reduced pressure (5 kPa) at a temperature in the region of 50° C. 1.48 cm3 of normal aqueous hydrochloric acid were added to the solid residue obtained, followed by 10 cm3 of water. The solution obtained was extracted with 5 times 20 cm3 of dichloromethane. The organic extracts were combined and then concentrated under reduced pressure (5 kPa). 0.189 g of (3R,4R)-4-[3-(6-methoxyquinolin-4-yl)propyl]-1-(prop-2-ynyl)piperidine-3-carboxylic acid was obtained in the form of a foam with a white color.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403610B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-c3dbb50a3b6f4eccb41af679a420e2fc |
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| Source note | uspto-grants-2002_06 |
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