HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Aminoquinoline → n-(6-Quinolinyl)quinuclidine-3-carboxamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Aminoquinoline | HCID 11373 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Quinuclidinecarbonyl chloride Hydrochloride | HCID 12673437 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | n-(6-Quinolinyl)quinuclidine-3-carboxamide hydrochloride | HCID 10149725 | — |
Reaction Steps
172 mg (1.19 mmol) of 6-aminoquinoline are mixed with 461 mg (3.57 mmol) of N,N-diisopropylethylamine in 3 ml of DMF under argon at 0° C. 250 mg (2.57 mmol) of 3-quinuclidinecarbonyl chloride hydrochloride are dissolved in a little dry DMF and added dropwise to the reaction mixture at 0° C. It is then stirred at room temperature overnight. It is worked up by concentrating and taking up in dichloromethane. The crude product is chromatographed on silica gel 60 (mobile phase: dichloromethane/ethyl acetate 10:1, then dichloromethane/methanol 10:1, 3:1). The product fractions are combined and finally purified by preparative HPLC (RP18 column; mobile phase: acetonitrile/water, gradient 1:99→30:70).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07247728B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-fc776fb3e8584746a568e2d06187f522 |
| Source note | uspto-grants-2007_07 |