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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189775Generated: October 25, 2026

6-(4-Methylpiperazin-1-yl)pyridin-3-amine → 8-Benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acid [6-(4-methyl-piperazin-1-yl)-pyridin-3-yl]-amide

https://huagongshe.com/reaction/1189775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(4-Methylpiperazin-1-yl)pyridin-3-amineHCID 2763390—
Reactant8-Benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acidHCID 66914636—
SolventDichloromethane methanolHCID 21226129—
Product8-Benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acid [6-(4-methyl-piperazin-1-yl)-pyridin-3-yl]-amideHCID 44515978—

Reaction Steps

The title compound was prepared in analogy to the procedure described in Step 14.1 but stirring the reaction mixture for 20 h at rt, using 6-(4-methylpiperazin-1-yl)-pyridin-3-ylamine (prepared as described in Example 33 but using N-methyl-piperazine in Step 33.2) and 8-benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acid (Example 59). Title compound: ESI-MS: 481.0 [M+H]+; tR=3.81 min (System 1); TLC: Rf=0.40 (DCM/MeOH, 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674099B2
Source datasetuspto-grants-2014_03
ORD IDord-5f384e5eb4e64537bed328c7dfad81e3
Source noteuspto-grants-2014_03