HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 2-(4-Cyclopropylpiperazin-1-yl)benzothiazole-6-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Cyclopropylpiperazine | HCID 4742004 | — |
| Reactant | 2-Chloro-1,3-benzothiazole-6-carbonitrile | HCID 21985859 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 2-(4-Cyclopropylpiperazin-1-yl)benzothiazole-6-carbonitrile | HCID 59588789 | 43% |
Reaction Steps
A suspension of 2-chlorobenzothiazole-6-carbonitrile (3.5 g, 18 mmol), 1-cyclopropylpiperazine (3.63 g, 28.8 mmol) and ammonium chloride (0.96 g, 18 mmol) in butan-1-ol (112 mL) was heated at reflux for 48 h. The solvent was removed under reduced pressure and the residue was diluted with water (30 mL). The mixture was made alkaline with potassium carbonate and extracted with CH2Cl2 (3×20 mL). The combined organic extracts were concenrated to give a residue which was purified by column chromatography on silica gel (20% ethyl acetate in petroleum ether) to give 2.2 g (43 5) of 2-(4-cyclopropylpiperazin-1-yl)benzothiazole-6-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394842B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-ba2688646505410394d5387b3ab02438 |
| Source note | uspto-grants-2013_03 |