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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716415Generated: November 3, 2026

1-Methylpiperazine → HCID 16059211, compound

https://huagongshe.com/reaction/1716415

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 16059210HCID 16059210—
ProductHCID 16059211HCID 1605921122%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 20 mg (0.041 mmol) of (1-benzyl-2-methyl-1H-indol-3-yl)-[4-(2-chloro-benzoimidazol-1-yl)-piperidin-1-yl]-methanone (the preparation of which is described in example 1) and N-methyl-piperazine was heated in a sealed tube at 90° C. for 8 hours, cooled to RT and then concentrated in vacuo. Flash chromatography (CH2Cl2/MeOH 9/1) afforded 5 mg (22%) of (1-benzyl-2-methyl-1H-indol-3-yl)-{4-[2-(4-methyl-piperazin-1-yl)-benzoimidazol-1-yl]-piperidin-1-yl}-methanone as white solid. ES-MS m/e (%): 547.5 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803815B2
Source datasetuspto-grants-2010_09
ORD IDord-ec0bc9abad99435587628696caab5aa1
Source noteuspto-grants-2010_09