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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388969Generated: October 30, 2026

Piperazine → HCID 68443918, compound

https://huagongshe.com/reaction/388969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 68445499HCID 68445499—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68443918HCID 68443918—

Reaction Steps

A solution of the amide from above (1 mmol) in dioxane (2 mL) was reacted with aqueous NH4OH using the conditions described in Example 115. After the formation of 4-amino-2-chloro-N-(5-methyl-1H-indazol-6-yl)-5-nitrobenzamide was complete, charged with piperazine (5 mmol). The contents were heated at reflux for 10 h and the reaction mixture was cooled to RT. The contents were poured onto ice cold water with vigorous stirring. The solid formed was collected by filtration, washed with water, and dried in vacuo to provide the product, 4-amino-N-(5-methyl-1H-indazol-6-yl)-5-nitro-2-piperazin-1-yl-benzamide as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377983B2
Source datasetuspto-grants-2013_02
ORD IDord-52adc6ac782e4bd184b7ffbe244ddb55
Source noteuspto-grants-2013_02