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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632590Generated: October 29, 2026

Benzenesulfonic Acid → HCID 131735435, compound

https://huagongshe.com/reaction/632590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic AcidHCID 7371—
ReactantHCID 71656881HCID 71656881—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 131735435HCID 13173543583.5%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321747B2
Source datasetuspto-grants-2016_04
ORD IDord-4b9a5dde98a64cbfa476acc90c3c11c2
Source noteuspto-grants-2016_04