HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545435Generated: October 31, 2026
HCID 67133043, compound → HCID 178519289, compound
https://huagongshe.com/reaction/545435
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67133043 | HCID 67133043 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178519289 | HCID 178519289 | 77.6% |
Reaction Steps
A solution of 0.07 g (0.1 mmol) of [5-(1-benzyl-1H-[1,2,4]triazol-3-yl)-3-cyclopropyl-2-(4-trifluoromethoxy-phenyl)-3H-imidazol-4-yl]-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanone (intermediate 12) and a generous spatula of 10% palladium on activated charcoal in 1 ml of MeOH made acidic by addition of a few drops of 25% HCl was stirred under one atmosphere of hydrogen for 16 h. Then, the mixture was filtered over Hyflo, concentrated and the residue taken up in CH2Cl2. The organic phase was washed with saturated sodium hydrogen carbonate solution, dried with sodium sulphate and concentrated. Purification by flash column chromatography [CH2Cl2/MeOH 9:1 to 8:2] afforded 0.04 g (64%) of the title compound as a colorless amorphous solid. MS: 516.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935707B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-d5a19051cf1a492887ebcb85789d54ab |
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| Source note | uspto-grants-2011_05 |
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