HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 5-fluoro-1-methyl-2-piperazin-1-yl-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-Chloro-5-fluoro-1-methyl-1H-benzimidazole | HCID 21985828 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 5-fluoro-1-methyl-2-piperazin-1-yl-1H-benzimidazole | HCID 22028248 | — |
Reaction Steps
0.7 g 2-chloro-5-fluoro-1-methyl-1H-benzimidazole and 1.3 g piperazine are suspended in 10 ml n-butanol and stirred for 48 hours at ambient temperature. The reaction mixture is evaporated to dryness and the product is purified by chromatography (aluminium oxide, methylene chloride/methanol 10/1). 0.73 g (V-8) are obtained as a solid. 1H NMR (400 MHz, DMSO): 6.9 (1H, t); 3.6 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637519B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-cfdb5f31942e4d3e870e8dc52a7ca39f |
| Source note | uspto-grants-2014_01 |