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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388953Generated: October 30, 2026

Ammonium Hydroxide → HCID 68444145, compound

https://huagongshe.com/reaction/388953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 68443945HCID 68443945—
ReactantHCID 68444790HCID 68444790—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68444145HCID 68444145—

Reaction Steps

A solution of N-benzothiazol-6-yl-2-chloro-4-fluoro-5-nitrobenzamide (2 mmol) in dioxane (4 mL) was reacted with aqueous NH4OH using the conditions described in Example 115. After the formation of 4-amino-N-benzothiazol-6-yl-2-chloro-5-nitrobenzamide was complete, the reaction mixture was charged with N-methylpiperazine (12 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-benzothiazol-6-yl-2-(4-methyl-piperazin-1-yl)-5-nitrobenzamide as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377983B2
Source datasetuspto-grants-2013_02
ORD IDord-647b94447de34cdd896511816fecd527
Source noteuspto-grants-2013_02