HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113068Generated: October 31, 2026
1,10-Phenanthroline → HCID 21071235, compound
https://huagongshe.com/reaction/2113068
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzyl (2-oxopiperidin-3-yl)carbamate | HCID 13556445 | — |
| Reactant | 1-(4-Iodophenyl)cyclopropane-1-carboxylic acid | HCID 21706477 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21071235 | HCID 21071235 | — |
Reaction Steps
Part A. To a mixture of (2-oxo-piperidin-3-yl)-carbamic acid benzyl ester (1.35 g, 5.44 mmol) and 1-(4-iodo-phenyl)-cyclopropanecarboxylic acid (1.56 g, 5.42 mmol, 1.0 eq) in DMSO (5 mL) was added K2CO3 (3.00 g, 21.73 mmol, 4.0 eq), CuI (0.52 g, 2.74 mmol, 0.5 eq), and 1,10-phenanthroline (0.50 g, 2.74 mmol, 0.5 eq) sequentially. The mixture was heated at 120° C. overnight under N2. After cooling, EtOAc and H2O was added. The mixture was filtered. The filtrate was washed with 1N NaOH. The aqueous layer was acidified with conc. HCl, and extracted with EtOAc (3×). The organics were washed with brine, dried over MgSO4, filtered, and concentrated to give crude 1-[4-(3-benzyloxycarbonyl-amino-2-oxo-piperidin-1-yl)-phenyl]-cyclopropanecarboxylic acid (0.69 g, slightly contaminated with disubstituted compound). LC/MS (ESI) 409.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524863B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-10870804bcc442fea890041807ea6e5b |
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| Source note | uspto-grants-2009_04 |
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