HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466144Generated: November 3, 2026
Dimethylformamide → 1-[2-(2,1,3-Benzoxadiazol-5-yl)ethyl]-4-[2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-2-one
https://huagongshe.com/reaction/1466144
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(2-Bromoethyl)-2-benzofuran-1(3H)-one | HCID 67513163 | — |
| Reactant | 1-[2-(2,1,3-Benzoxadiazol-5-yl)ethyl]-2-piperazinone | HCID 89526184 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-[2-(2,1,3-Benzoxadiazol-5-yl)ethyl]-4-[2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-2-one | HCID 117599340 | — |
Reaction Steps
A mixture of 1-[2-(2,1,3-Benzoxadiazol-5-yl)ethyl]piperazin-2-one (54 mg, 0.22 mmol), 5-(2-Bromoethyl)-2-benzofuran-1(3H)-one (105 mg, 0.44 mol), Triethylamine (0.15 mL, 1.1 mmol), and DMF (1.5 mL) was heated to 60° C. for 24 hours. The reaction was diluted with EtOAc, washed with water and brine, dried over MgSO4, and purified by prep-TLC (5% MeOH in DCM) to deliver the title product. LC-MS (IE, m/z): 407 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999990B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-c57cace3171b47c0992b1ce7cd99b956 |
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| Source note | uspto-grants-2015_04 |
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