HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187128Generated: November 2, 2026
HCID 59568679, compound → HCID 59568718, compound
https://huagongshe.com/reaction/1187128
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59568679 | HCID 59568679 | — |
| Reactant | HCID 68432653 | HCID 68432653 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59568718 | HCID 59568718 | — |
Reaction Steps
To a 5 ml microwave tube were added 5-(bromoacetyl)-4,6-dimethyl-2-benzofuran-1(3H)-one (0.220 g, 0.777 mmol), 1-[(2R)-2-hydroxy-2-(4-methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-1-ium chloride (0.215 g, 0.777 mmol), and a stir bar; the mixture was dissolved in THF (2 mL). The tube was capped, degassed and purged with N2. The tube was then placed in an oil bath and heated at 50° C. for 12 h; LC indicated formation of the desired product. The solution was concentrated to dryness, dissolved in MeOH (3.6 mL), filtered and was then subjected to purification by mass-directed HPLC to give 5-({4-[(2R)-2-hydroxy-2-(4-methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-1-yl}acetyl)-4,6-dimethyl-2-benzofuran-1(3H)-one. LC-MS (IE, m/z): 479 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673920B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-5d2ba7a6b6cb4c2fbf76398096145eb2 |
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| Source note | uspto-grants-2014_03 |
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