HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 6-Chloro-2-(piperazin-1-yl)-1,3-benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Dichlorobenzothiazole | HCID 77176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Chloro-2-(piperazin-1-yl)-1,3-benzothiazole | HCID 2746595 | 100% |
Reaction Steps
To a stirred solution of 1.07 g (5.24 mmol) of 2,6-dichlorobenzothiazole in dry DMF (25 mL) was added 2.4 g of potassium carbonate (15.7 mmol) and 0.5 g of piperazine (5.8 mmol). The mixture was stirred at room temperature for 4 h. When the reaction was complete it was partitioned between EtOAc (150 mL) and water (50 mL) and separated. The aqueous layer was extracted with EtOAC (2×100 mL). The combined organic layers were then washed with water (2×25 mL), brine, dried over Na2SO4, and the solvent was removed under reduced pressure to give 1.33 g (100%) of desired product as a white solid. MS (electrospray): exact mass calculated for C11H12CIN3S, 253.04; m/z found, 254.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07388011B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-194561370f28496e95436e2998a266d2 |
| Source note | uspto-grants-2008_06 |