HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 3-(Piperazin-1-yl)-1,2-benzoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 3-Chloro-1,2-benzoxazole | HCID 2779780 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-(Piperazin-1-yl)-1,2-benzoxazole | HCID 13232475 | 76% |
Reaction Steps
3-Chloro-1,2-benzisoxazole reacted with excess piperazine in the presence of pyridine to provide 3-(piperazin-1-yl)benzo[d]isoxazole (3A) in 76% yield. Reductive amination of compound (3A) with 2-carbomethoxy 2-methyl propionaldehyde gave alkylated piperazine (4A), which was purified over silica gel. Basic hydrolysis of the methyl ester of (4A) in aqueous ethanol followed by acidification gave the carboxylic acid (1) as the mono-HCl salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088778B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-cae11d1a78c943df9591b7e68e4c0f79 |
| Source note | uspto-grants-2012_01 |