HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632593Generated: October 29, 2026
Hydrochloric Acid → (5S)-4-(4,4-Difluorocyclohexyl)-2-[1-(5-{[(2S)-2,3-dihydroxypropyl]oxy}pyrimidin-2-yl)piperidin-4-yl]-3-{(S)-fluoro[4-(trifluoromethyl)phenyl]methyl}-7,7-dimethyl-5,6,7,8-tetrahydroquinolin-5-ol dihydrochloride
https://huagongshe.com/reaction/632593
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 71657166 | HCID 71657166 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (5S)-4-(4,4-Difluorocyclohexyl)-2-[1-(5-{[(2S)-2,3-dihydroxypropyl]oxy}pyrimidin-2-yl)piperidin-4-yl]-3-{(S)-fluoro[4-(trifluoromethyl)phenyl]methyl}-7,7-dimethyl-5,6,7,8-tetrahydroquinolin-5-ol dihydrochloride | HCID 71657165 | 66% |
Reaction Steps
To a solution of 36.2 mg (50.1 μmol) of (5S)-4-(4,4-Difluorocyclohexyl)-2-[1-(5-{[(2S)-2,3-dihydroxypropyl]oxy}pyrimidin-2-yl)piperidin-4-yl]-3-{(S)-fluoro[4-(trifluoromethyl)phenyl]methyl}-7,7-dimethyl-5,6,7,8-tetrahydroquinolin-5-ol, which was prepared by a method similar to that of Reference Example 25, in 0.36 ml of acetone, 9.2 μl (110 μmol) of 35% hydrochloric acid was added dropwise with stirring at 45° C., and the mixture was stirred for 10 minutes. Then, stirring was continued at room temperature for 30 minutes, and the precipitated solid was obtained by filtration, washed with acetone and then dried under reduced pressure at 40° C. to provide 26.3 mg of the title compound as a white powder (yield: 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321747B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-f06fea0f3c4f40419df3476b96f6500d |
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| Source note | uspto-grants-2016_04 |
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