HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922539Generated: October 25, 2026
hydrogen chloride CPME → N-(4-{trans-2-[(2-phenylpiperidin-4-yl)amino]cyclopropyl}phenyl)-3-(trifluoromethyl)benzamide dihydrochloride
https://huagongshe.com/reaction/922539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | hydrogen chloride CPME | HCID 66926893 | — |
| Reactant | Tert-butyl 2-phenyl-4-{[trans-2-(4-{[3-(trifluoromethyl)benzoyl]amino}phenyl)cyclopropyl]amino}-piperidine-1-carboxylate | HCID 86729901 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-{trans-2-[(2-phenylpiperidin-4-yl)amino]cyclopropyl}phenyl)-3-(trifluoromethyl)benzamide dihydrochloride | HCID 86729902 | — |
Reaction Steps
tert-Butyl 2-phenyl-4-{[trans-2-(4-{[3-(trifluoromethyl)benzoyl]amino}phenyl)cyclopropyl]amino}-piperidine-1-carboxylate (62 mg) was dissolved in THF (0.5 mL), and the mixture was ice-cooled to 0° C. 4N Hydrochloric acid/cyclopentyl methyl ether solution (5.0 mL) was added, and the mixture was stirred at room temperature overnight. The solvent was evaporated under reduced pressure. The residue was recrystallized from methanol/diisopropyl ether to give the title compound (24 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278931B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-b25bf44b8300471eb1fb2b2cbc70396c |
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| Source note | uspto-grants-2016_03 |
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