HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Fluoro-2-{[2-(piperazin-1-yl)ethyl]sulfanyl}-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-[2-(5-Fluorobenzimidazol-2-ylthio)ethyl]-4-formylpiperazine | HCID 23116158 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Fluoro-2-{[2-(piperazin-1-yl)ethyl]sulfanyl}-1H-benzimidazole | HCID 23116156 | 81.8% |
Reaction Steps
1-[2-(5-Fluorobenzimidazol-2-ylthio)ethyl]-4-formylpiperazine (1.80 g, 5.8 mmol) was dissolved in methanol (20 mL), 12N hydrochloric acid (2 mL) was added thereto, followed by stirring for 18 hours at room temperature. The reaction mixture was concentrated under reduced pressure, and saturated ammonia-methanol was added thereto, followed by stirring for five minutes at room temperature. The solvent was removed under reduced pressure, and the residue was purified through silica gel column chromatography (chloroform: saturated ammonia-methanol=100:3), to thereby yield 1-[2-(5-fluorobenzimidazol-2-ylthio)ethyl]piperazine (1.33 g, yield 81%) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07223764B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-1a3fe4954d1548029244b48e0b0733ab |
| Source note | uspto-grants-2007_05 |