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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716874Generated: October 25, 2026

1-(3-Chlorophenyl)piperazine → Methyl 3-(4-(3-chlorophenyl)piperazin-1-yl)-2-phenylquinoxaline-6-carboxylate

https://huagongshe.com/reaction/716874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Chlorophenyl)piperazineHCID 1355—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 3-bromo-2-phenylquinoxaline-6-carboxylateHCID 86667202—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(4-(3-chlorophenyl)piperazin-1-yl)-2-phenylquinoxaline-6-carboxylateHCID 6704168592.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of methyl 3-bromo-2-phenylquinoxaline-6-carboxylate (150 mg, 0.44 mmol, 1.00 equiv), 1-(3-chlorophenyl)piperazine (172.5 mg, 0.88 mmol, 2.00 equiv), and DIEA (170.3 mg, 1.32 mmol, 3.00 equiv) in DMF (4 mL) was placed in a 20-mL sealed tube and stirred overnight at 100° C. in an oil bath, then quenched with water. The resulting solution was extracted with 6×20 mL of ethyl acetate, the organic layers combined and dried over anhydrous sodium sulfate, filtered to remove solids, and concentrated under vacuum. Purification via silica gel column (PE/EA (30:1)) yielded 186.7 mg (89%) of methyl 3-(4-(3-chlorophenyl)piperazin-1-yl)-2-phenylquinoxaline-6-carboxylate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193693B2
Source datasetuspto-grants-2015_11
ORD IDord-8a88c13c467145e083b4715d6ecb9c23
Source noteuspto-grants-2015_11