HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Tert-butyl-6-nitro-5-[4-phenylpiperazin-1-yl]benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | 2-Tert-butyl-5-chloro-6-nitrobenzothiazole | HCID 19794202 | — |
| Product | 2-Tert-butyl-6-nitro-5-[4-phenylpiperazin-1-yl]benzothiazole | HCID 20192955 | — |
Reaction Steps
A mixture of 7 g of 2-tert-butyl-5-chloro-6-nitrobenzothiazole described in Example 5, in 8.2 g of N-phenylpiperazine is heated at 150°-160° for 12 hours, cooled and poured into water. The paste is extracted with methylene chloride, washed with 2N HCl, then with 10% NaOH and then with water. The organic layer is dried, the solvent evaporated and the solid crystallised from isopropyl alcohol to give 2-tert-butyl-6-nitro-5-[4-phenylpiperazin-1-yl]benzothiazole, melting at 152°-155°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04680301 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-d21f091a14494fe698eebfb69a479ee2 |
| Source note | uspto-grants-1987_07 |