HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409923Generated: October 31, 2026
HCID 71233209, compound → HCID 71233212, compound
https://huagongshe.com/reaction/2409923
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 71233209 | HCID 71233209 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 71233212 | HCID 71233212 | 78% |
Reaction Steps
To a solution of benzyl ((1R,2R)-2-(((S)-3-methyl-1-(4-(trifluoromethyl)phenyl)piperidin-3-yl)amino)cyclohexyl)carbamate (420 mg, 0.858 mmol) in MeOH (4 mL) was added palladium on carbon (10%) (84 mg, 0.789 mmol) under nitrogen atmosphere. The resultant black color suspension was stirred under hydrogen balloon pressure at RT for 2 h. The reaction mass was filtered on Celite and the filter cake was washed with methanol (3×5 mL). The filtrate was concentrated and dried under vacuum to get (1R,2R)—N1-((S)-3-methyl-1-(4-(trifluoromethyl)phenyl)piperidin-3-yl)cyclohexane-1,2-diamine (300 mg, 0.667 mmol, 78% yield) as off white solid. This was directly used for next reaction with out any further purification. Anal. Calcd. for C19H28F3N3 m/z 355.4, found: 490.4 (M+H)+; This was taken for next step with out any further characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815909B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-1d3f0eb220fb445a8e087a717f610510 |
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| Source note | uspto-grants-2014_08 |
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