HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 6-Bromo-2-(4-cyclopropylpiperazin-1-yl)benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Bromo-2-chlorobenzothiazole | HCID 2049871 | — |
| Reactant | 1-Cyclopropylpiperazine | HCID 4742004 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Bromo-2-(4-cyclopropylpiperazin-1-yl)benzothiazole | HCID 59588803 | 31% |
Reaction Steps
To a solution of 6-bromo-2-chlorobenzothiazole (8.2 g, 33 mmol) in EtOH (115 mL) was added Et3N (16.7 g, 165 mmol), followed by 1-cyclopropylpiperazine (5 g, 39.6 mmol). The mixture was heated at reflux for 12 h. Then the mixture was evaporated to remove EtOH. Water (120 mL) was added to the residue and the mixture was extracted with CH2Cl2 (3×50 mL). The combined organic extracts were washed with brine, dried (Na2SO4) and concentrated to give a residue, which was purified by column chromatography on silica gel eluting with a mixture of EtOAc/petroleum ether (1:10 with 0.1% NH4OH added) to give 3.46 g (31%) 6-bromo-2-(4-cyclopropylpiperazin-1-yl)benzothiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772285B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-95b29f0564e64845bc24b4586d38f84e |
| Source note | uspto-grants-2014_07 |