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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519644Generated: November 3, 2026

Sodium triacetoxyborohydride → HCID 56970864, compound

https://huagongshe.com/reaction/1519644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-[2-(piperazin-1-yl)ethyl]-2-benzofuran-1(3H)-oneHCID 59568671—
ReactantHCID 86694487HCID 86694487—
SolventDichloromethaneHCID 6344—
ProductHCID 56970864HCID 56970864—

Reaction Steps

A solution of crude 2-(cyclopropyloxy)-4-(2-oxoethyl)benzonitrile (80 mg, 0.4 mmol), 5-(2-piperazin-1-ylethyl)-2-benzofuran-1(3H)-one (150 mg, 0.6 mmol) and NaBH(OAc)3 (400 mg, 2 mmol) in 10 mL of anhydrous DCM was stirred at ambient temperature overnight. The reaction mixture was added 50 mL of DCM and washed with brine. The organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified with prep-TLC to afford 2-(cyclopropyloxy)-4-(2-{4-[2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-1-yl}ethyl)benzonitrile. 1H-NMR (400 MHz, CDCl3) δ ppm 7.77 (d, J=7.8 Hz, 1H), 7.37 (d, J=7.8 Hz, 1H), 7.31 (d, J=7.8 Hz, 1H), 7.27 (s, 1H), 7.11 (s, 1H), 6.78˜6.80 (m, 1H), 5.22 (s, 2H), 2.42˜2.93 (m, 17H), 0.77˜0.80 (m, 4H). (0.28 μM)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073882B2
Source datasetuspto-grants-2015_07
ORD IDord-dbefc149f9a84692bdfde709030083ee
Source noteuspto-grants-2015_07