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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187128Generated: November 2, 2026

HCID 59568679, compound → HCID 59568718, compound

https://huagongshe.com/reaction/1187128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59568679HCID 59568679—
ReactantHCID 68432653HCID 68432653—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59568718HCID 59568718—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673920B2
Source datasetuspto-grants-2014_03
ORD IDord-5d2ba7a6b6cb4c2fbf76398096145eb2
Source noteuspto-grants-2014_03