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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519619Generated: November 3, 2026

Sodium cyanoborohydride → 5-Fluoro-2-methoxy-4-(2-{4-[2-(4-methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-1-yl}ethyl)benzonitrile

https://huagongshe.com/reaction/1519619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5-[2-(piperazin-1-yl)ethyl]-2-benzofuran-1(3H)-oneHCID 59568671—
Reactant5-Fluoro-2-methoxy-4-(2-oxoethyl)benzonitrileHCID 86694458—
SolventMethanolHCID 887—
Product5-Fluoro-2-methoxy-4-(2-{4-[2-(4-methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-1-yl}ethyl)benzonitrileHCID 68071886—

Reaction Steps

To a mixture of 5-[2-(piperazin-1-yl)ethyl]-2-benzofuran-1(3H)-one (95 mg, 0.27 mmol) and 5-fluoro-2-methoxy-4-(2-oxoethyl)benzonitrile (40 mg, 0.23 mmol) in methanol (1.0 mL) at 0° C. was added sodium cyanoborohydride (20 mg, 0.32 mmol) and the mixture was stirred at room temperature for 12 hours. The reaction mixture was concentrated and purified by mass-directed HPLC to provide 5-fluoro-2-methoxy-4-(2-{4-[2-(4-methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-1-yl}ethyl)benzonitrile. LC-MS (IE, m/z): 438.4 [M+1]+. (0.034 μM)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073882B2
Source datasetuspto-grants-2015_07
ORD IDord-2e32292d4b834c6cba262b0bcb2eeb55
Source noteuspto-grants-2015_07