HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 68443918, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 68445499 | HCID 68445499 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68443918 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820821B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-e961a6c291dc44db92508405f9eabf2f |
| Source note | uspto-grants-2010_10 |