HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465745Generated: October 30, 2026
Potassium Phosphate, Tribasic → tert-Butyl 4-(7-bromo-2-naphthyl)-3-oxopiperazine-1-carboxylate
https://huagongshe.com/reaction/1465745
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-N,2-N-dimethylcyclohexane-1,2-diamine | HCID 551074 | — |
| Reactant | 2,7-Dibromonaphthalene | HCID 625355 | — |
| Reactant | Tert-butyl 3-oxopiperazine-1-carboxylate | HCID 3157178 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | tert-Butyl 4-(7-bromo-2-naphthyl)-3-oxopiperazine-1-carboxylate | HCID 131732665 | — |
Reaction Steps
To a 20 mL microwave vial charged with 2,7-dibromonaphthalene (1.1 g, 3.8 mmol), tert-butyl 3-oxopiperazine-1-carboxylate (0.50 g, 2.5 mmol), and a stir bar was added copper (I) iodide (95 mg, 0.50 mmol), N,N′-dimethylcyclohexane-1,2-diamine (142 mg, 1.0 mmol), K3PO4 (1100 mg, 5.0 mmol), and dioxane (15 mL). The mixture was purged three times with nitrogen, and heated to 150° C. in a microwave reactor. The crude solution was diluted with EtOAc, adsorbed onto silica gel, and purified by silica gel chromatography (Hex:EtOAc). The solvent was removed to provide the title compound. LC-MS (IE, m/z): 405 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999991B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-c0d3925e28e445d2a7e268e18f092f10 |
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| Source note | uspto-grants-2015_04 |
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