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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254190Generated: October 31, 2026

1-Methylpiperazine → HCID 21854014, compound

https://huagongshe.com/reaction/254190

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantOxalyl chlorideHCID 65578—
ReactantIndole-3-Carboxylic AcidHCID 69867—
SolventDichloromethaneHCID 6344—
ProductHCID 21854014HCID 21854014—

Reaction Steps

1H-Indole-3-carboxylic acid (1.61 g, 0.01 moles) was stirred with oxalyl chloride (0.99 g, 0.011 moles) in 20 mL dichloromethane at 0 to 25° C. for 3-4 hours. After completion of the reaction (TLC), volatile substances were distilled off under the reduced pressure. The residue was taken in 20 mL dichloroethane and to this stirred solution, was added N-methylpiperazine (1.1 g, 0.011 moles). The reaction mixture was further stirred for next 3-5 hours, till the reaction completes (TLC). Reaction mixture was diluted with dichloromethane 20 mL), washed with water, brine and saturated solution of sodium bicarbonate. The organic layer was dried over sodium sulfate and the organic solvents were evaporated under vacuo. The product was purified using column chromatography on silica gel G stationary phase and suitable combinations of ethyl acetate and methanol in increasing gradient, as the mobile phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875605B2
Source datasetuspto-grants-2011_01
ORD IDord-cc4e0ab2ff76430bafd695424be4e25e
Source noteuspto-grants-2011_01