HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 2-Tert-butyl-6-nitro-5-[piperazin-1-yl]benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-Tert-butyl-5-chloro-6-nitrobenzothiazole | HCID 19794202 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Tert-butyl-6-nitro-5-[piperazin-1-yl]benzothiazole | HCID 20192922 | — |
Reaction Steps
A solution of 13.5 g of 2-tert-butyl-5-chloro-6-nitrobenzothiazole described in Example 5, and 40 g of anhydrous piperazine in 100 ml of dimethylsulphoxide is heated at 140° for 2 hours, cooled and poured into ice-water. The yellow solid is filtered, washed with water and dried at 80° to yield 2-tert-butyl-6-nitro-5-[piperazin-1-yl]benzothiazole, melting at 144°-146°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04680301 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-ac16951992334c82be030710957fc663 |
| Source note | uspto-grants-1987_07 |