HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497429Generated: October 30, 2026
1,10-Phenanthroline → HCID 86759850, compound
https://huagongshe.com/reaction/497429
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzyl [(1H-imidazol-2-yl)methyl]methylcarbamate | HCID 12125407 | — |
| Reactant | HCID 86759851 | HCID 86759851 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 86759850 | HCID 86759850 | 66.9% |
Reaction Steps
Benzyl 1H-imidazol-2-ylmethyl(methyl)carbamat (1.17 g, 4.76 mmol) from Part E, 1-[2-trifluoroacetamidomethyl-phenyl]-3-trifluoromethyl-6-[4-Iodo-2-fluorophenyl]-1,4,5,6-tetrahydropyrazolo-[3,4-c]-pyridin-7-one from Part D (1.63 g, 3.18 mmol), CuI (0.12 9, 20%), K2CO3 (0.66 g, 4.76 mmol), 1,10-phenanthroline (56 mg, 20%) were added together with 100 mL of DMSO. The mixture was degassed and then heated at 130° C. under N2 for 12 h. The mixture was cooled and aqueous NH4OH (200 mL of of 10% NH4OH) was added. The mixture was filtered through Celite® and washed with EtOAc. The two layers were separated and the aqueous layer was extracted with EtOAc. The combined EtOAc mixture was washed with brine, dried over MgSO4, concentrated, and chromatographed with EtOAc to give 1.34 g of the desired product (66.9%). MS (ES+): 631.3, (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06949550B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-8373de6249c24b8faf730d386b505b64 |
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| Source note | uspto-grants-2005_09 |
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