HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 2-Piperazin-1-yl-1,3-benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chlorobenzothiazole | HCID 11987 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Piperazin-1-yl-1,3-benzothiazole | HCID 592122 | — |
Reaction Steps
A solution of 1.7 g (0.01 mol) of 2-chlorobenzothiazole, 4.76 g (0.05 mol) of piperazine and 7 ml (0.05 mol) of triethylamine in 50 ml of ethanol is stirred for 48 hours at ambient temperature. The reaction mixture is concentrated by evaporation, mixed with water and extracted twice with dichloromethane. The combined organic phases are dried over sodium sulphate, the drying agent is filtered off and the filtrate is concentrated by evaporation. The residue is washed with diethylether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06821967B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-420e8e4315cd41a2b67845937dd71983 |
| Source note | uspto-grants-2004_11 |