HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 6-Bromo-2-piperazin-1-yl-1,3-benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-Bromo-2-chlorobenzothiazole | HCID 2049871 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6-Bromo-2-piperazin-1-yl-1,3-benzothiazole | HCID 42281675 | — |
Reaction Steps
2-Chloro-6-bromobenzothiazole (2.29 g), piperazine (1.59 g) and sodium bicarbonate (3.10 g) were combined in isopropanol (75 mL) and the resulting orange solution was heated to reflux overnight, then concentrated to ˜15 mL, diluted with water, and extracted with DCM. The extracts were concentrated to yield an orange solid which was chromatographed (0 to 5% MeOH in DCM) to yield 6-bromo-2-(piperazin-1-yl)benzo[d]thiazole as a slightly pink solid. MS: 297.9 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481547B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-05bc984d4429494597eea9b37cc37540 |
| Source note | uspto-grants-2013_07 |