HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632590Generated: October 29, 2026
Benzenesulfonic Acid → HCID 131735435, compound
https://huagongshe.com/reaction/632590
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonic Acid | HCID 7371 | — |
| Reactant | HCID 71656881 | HCID 71656881 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 131735435 | HCID 131735435 | 83.5% |
Reaction Steps
To a solution of 30.0 mg (0.0408 mmol) of (5S)-4-(4,4-Difluorocyclohexyl)-3-{(S)-fluoro[4-(trifluoromethyl)phenyl]methyl}-2-{1-[5-(3-hydroxy-3-methylbutoxy)pyrimidin-2-yl]piperidin-4-yl}-7,7-dimethyl-5,6,7,8-tetrahydroquinolin-5-ol, which was prepared by a method similar to that of Reference Example 16, in 0.4 ml of tert-butyl methyl ether, 0.013 ml (0.041 mmol) of 3.16 M benzenesulfonic acid aqueous solution was added dropwise with stirring at 40° C. Then, the reaction mixture was cooled to room temperature and stirred for 30 minutes. The precipitated solid was obtained by filtration, washed with tert-butyl methyl ether and then dried under reduced pressure at 60° C. to provide 29.8 mg of the title compound as a white powder (yield: 82%).
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-4b9a5dde98a64cbfa476acc90c3c11c2 |
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| Source note | uspto-grants-2016_04 |
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