HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645194Generated: November 1, 2026
HCID 66775543, compound → HCID 66775371, compound
https://huagongshe.com/reaction/1645194
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 66775543 | HCID 66775543 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66775371 | HCID 66775371 | 100.3% |
Reaction Steps
To a par bottle charged with benzyl 2-(6-((N-(3-(trifluoromethoxy)benzyl)-1-methyl-1H-imidazole-4-carboxamido)methyl)-3-aza-bicyclo[3.1.0]hexan-3-yl)acetate (2.7 gm, 5.07 mmol) in 80 mL CH3OH, was added 300 mg palladium hydroxide on carbon (20%). The mixture was hydrogenated under 40 psi H2 at room temperature for 1 hour. The mixture was filtered over a celite, the celite pad was washed with CH3OH and the resulting solution was concentrated to yield 2.3 gm of 2-(6-((N-(3-(trifluoromethoxy)benzyl)-1-methyl-1H-imidazole-4-carboxamido)methyl)-3-aza-bicyclo[3.1.0]hexan-3-yl)acetic acid as a yellow solid; 400 MHz 1H NMR (CDCl3) δ 7.54 (s, 1H), 7.23-7.33 (m, 3H), 7.15 (s, 1H), 7.05 (d, J=7.9 Hz, 1H), 5.4 (brs, 2H), 4.81 (brs, 1H), 3.96 (brs, 1H), 3.68 (s, 3H), 3.49 (s, 2H), 3.28 (brs, 1H), 3.12 (brs, 2H), 1.76 (brs, 1H), 1.66 (brs, 2H); MS (M+1) 452.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124639B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-dab18566e7934afcada6985ab560d47e |
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| Source note | uspto-grants-2012_02 |
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