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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173442Generated: October 31, 2026

1,2-Dichloroethane → HCID 67517720, compound

https://huagongshe.com/reaction/2173442

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant5-(2-piperazin-1-ylethyl)-2-benzofuran-1(3H)-one hydrochlorideHCID 66646732—
ReactantHCID 67517397HCID 67517397—
SolventDichloromethaneHCID 6344—
ProductHCID 67517720HCID 67517720—

Reaction Steps

A solution of [2-ethenyl-4-(1H-tetrazol-1-yl)phenyl]acetic acid (43 mg, 0.19 mmol) in 10 mL of anhydrous DCM was added 5-[2-(piperazin-1-yl)ethyl]-2-benzofuran-1(3H)-one hydrochloride (53 mg, 0.19 mmol), EDC (56 mg, 0.28 mmol), HOBt (38 mg, 0.28 mmol), TEA (115 mg, 1.14 mmol) and then stirred at ambient temperature overnight. Then DCM was added and then mixture was washed with brine, dried over anhydrous Na2SO4 and concentrated. The residue was purified by prep-TLC to afford 5-[2-(4-{[2-ethenyl-4-(1H-tetrazol-1-yl)phenyl]acetyl}piperazin-1-yl)ethyl]-2-benzofuran-1(3H)-one. 1H-NMR (400 MHz, CDCl3) δ ppm 9.0 (s, 1H), 7.75˜7.78 (m, 2H), 7.48˜7.51 (m, 1H), 7.26˜7.31 (m, 3H), 6.76˜6.84 (rn, 1H), 5.7 (d, J=17.2 Hz, 1H), 5.44 (d, J=10.9 Hz, 1H), 5.22 (s, 2H), 3.75 (s, 2H), 3.6˜3.65 (m, 2H), 3.45˜3.48 (m, 2H), 2.86˜2.9 (m, 2H), 2.59˜2.64 (m, 2H), 2.41˜2.5 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-dc8c9a94e1714875b6591579fea2450b
Source noteuspto-grants-2015_06