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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466144Generated: November 3, 2026

Dimethylformamide → 1-[2-(2,1,3-Benzoxadiazol-5-yl)ethyl]-4-[2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-2-one

https://huagongshe.com/reaction/1466144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant5-(2-Bromoethyl)-2-benzofuran-1(3H)-oneHCID 67513163—
Reactant1-[2-(2,1,3-Benzoxadiazol-5-yl)ethyl]-2-piperazinoneHCID 89526184—
SolventEthyl AcetateHCID 8857—
Product1-[2-(2,1,3-Benzoxadiazol-5-yl)ethyl]-4-[2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-2-oneHCID 117599340—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-[2-(2,1,3-Benzoxadiazol-5-yl)ethyl]piperazin-2-one (54 mg, 0.22 mmol), 5-(2-Bromoethyl)-2-benzofuran-1(3H)-one (105 mg, 0.44 mol), Triethylamine (0.15 mL, 1.1 mmol), and DMF (1.5 mL) was heated to 60° C. for 24 hours. The reaction was diluted with EtOAc, washed with water and brine, dried over MgSO4, and purified by prep-TLC (5% MeOH in DCM) to deliver the title product. LC-MS (IE, m/z): 407 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999990B2
Source datasetuspto-grants-2015_04
ORD IDord-c57cace3171b47c0992b1ce7cd99b956
Source noteuspto-grants-2015_04