HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 11201996, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2,6-dichloro-N-(cyclohexylmethyl)-5-quinolinecarboxamide | HCID 86013022 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11201996 | HCID 11201996 | 80.7% |
Reaction Steps
A stirred solution of 2,6-dichloro-N-(cyclohexylmethyl)quinoline-5-carboxamide (Example 43 (a)) (200 mg) and piperazine (160 mg) in acetonitrile (2 mL) was heated at 80° C. in a CEM Discover microwave for 1 hour after which it was cooled to room temperature and concentrated. The residue was purified (Waters' SCX resin, ammonia in methanol (7 M) as eluant) and the resultant product was converted to the dihydrochloride salt by treatment with hydrochloric acid (4M in 1,4-dioxane). Recrystallisation (methanol/ethyl acetate) afforded the title compound as a solid (110 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07408065B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-8fe27363cd784db28322b139749aeb9b |
| Source note | uspto-grants-2008_08 |