HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797001Generated: November 2, 2026
HCID 178418361, compound → HCID 178509631, compound
https://huagongshe.com/reaction/1797001
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178522787 | HCID 178522787 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Product | HCID 178509631 | HCID 178509631 | — |
Reaction Steps
An ethanolic solution of {4-[4-(3-Trifluoromethyl-phenyl)-1H-imidazol-2-yl]-cyclohexylmethyl}-carbamic acid benzyl ester (4.15 g, 0.0091 mol) and 10% Pd/Carbon (400 mg) was shaken overnight under 55 psi of hydrogen in a Paar apparatus. The mixture was filtered through celite and concentrated under reduced pressure to give a foam, which was triturated with EtOAc/Hexanes/MeOH to produce C-{4-[4-(3-trifluoromethyl-phenyl)-1H-imidazole-2-yl]-cyclohexyl}-methylamine as a filterable solid. 1H NMR (DMSO-d6): δ 0.93–1.05 (m, 2H), 1.30–1.4 (m, 2H), 1.42–1.55 (m, 2H), 1.85 (d, J=12.8 Hz, 2H), 1.99 (d, J=11.6 Hz, 2H), 2.4–2.5 (m, 1H), 2.56–2.66 (m, 1H), 7.43–7.48 (m, 1H), 7.50–7.55 (m, 1H), 7.63 (s, 1H), 7.99 (d, J=7.9 Hz, 1H), 8.02 (s, 1H). MS 324 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07034034B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-83d1f0e41d0a486f9f7b84b61b806266 |
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| Source note | uspto-grants-2006_04 |
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