HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715844Generated: October 30, 2026
Hydrochloric Acid → HCID 76372213, compound
https://huagongshe.com/reaction/715844
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86682424 | HCID 86682424 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 76372213 | HCID 76372213 | 86.5% |
Reaction Steps
To a solution of 1.28 g (1.70 mmol) of (−)-4-(4,4-Difluorocyclohexyl)-3-{fluoro[4-(trifluoromethyl)phenyl]methyl}-5-[(4-methoxybenzyl)oxy]-7,7-dimethyl-2-[1-(pyrimidin-2-yl)piperidin-4-yl]-5,6,7,8-tetrahydroquinoline, which was prepared by a method similar to that of Reference Example 15, in 8 ml of 1,4-dioxane, 4 ml of 6 N hydrochloric acid was added, and the reaction solution was stirred at 70° C. for 3 hours. After completion of the reaction, the reaction solution was poured into saturated sodium hydrogencarbonate aqueous solution and extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride aqueous solution and dried with anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. n-Heptane was added to the obtained residue and the precipitate was obtained by filtration to provide 0.93 g of the title compound as a white solid (yield: 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187450B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-e1d3dbcd768e4e4f8f7531bfdf05dc7d |
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| Source note | uspto-grants-2015_11 |
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