HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519601Generated: November 1, 2026
Triethylamine → 5-{2-[4-(5,6,7,8-Tetrahydronaphtho[2,3-c][1,2,5]oxadiazol-6-yl)piperazin-1-yl]ethyl}-2-benzofuran-1(3H)-one
https://huagongshe.com/reaction/1519601
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(2-Bromoethyl)-2-benzofuran-1(3H)-one | HCID 67513163 | — |
| Reactant | 6-Piperazin-1-yl-5,6,7,8-tetrahydronaphtho[2,3-c][1,2,5]oxadiazole hydrochloride | HCID 86694449 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-{2-[4-(5,6,7,8-Tetrahydronaphtho[2,3-c][1,2,5]oxadiazol-6-yl)piperazin-1-yl]ethyl}-2-benzofuran-1(3H)-one | HCID 68071677 | — |
Reaction Steps
To a solution of 6-Piperazin-1-yl-5,6,7,8-tetrahydronaphtho[2,3-c][1,2,5]oxadiazole hydrochloride (20 mg, 0.068 mmol), 5-(2-bromoethyl)-2-benzofuran-1(3H)-one (33 mg, 0.14 mmol), and tetrabutylammonium iodide (2.5 mg, 6.8 umol) in DMF (2 mL) was added triethylamine (0.028 mL, 0.20 mmol). The mixture was heated to 55° C. for 6 hours. LC showed formation of the desired product, which was separated by mass-directed HPLC. LC-MS (IE, m/z): 419 [M+1]+. (0.21 μM)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073882B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-89d291171bcb478194f7939caa2ef695 |
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| Source note | uspto-grants-2015_07 |
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