HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 18182346, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Ethynyl-1-azabicyclo[2.2.2]octan-3-ol | HCID 3613517 | — |
| Reactant | HCID 18182263 | HCID 18182263 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18182346 | HCID 18182346 | 57% |
Reaction Steps
A mixture of 720 mg of 2-benzyl-3-bromo-6-(2-methoxyethyloxy)pyridine, 340 mg of 3-ethynyl-3-quinuclidinol, 130 mg of tetrakis(triphenylphosphine)palladium(0), 42 mg of cuprous iodide, 0.93 ml of triethylamine and 3 ml of N,N-dimethylformamide was heated under stirring in an oil bath kept at 80° C. for 2 hours in a nitrogen atmosphere. After cooling as it was, the mixture was extracted with ethyl acetate-dilute aqueous ammonia. The organic phase was washed with water and brine, dried over anhydrous magnesium sulfate and evaporated. The residue was subjected to NH-silica gel column chromatography and eluted with 20-100% ethyl acetate/hexane and then with 2.5% methanol/ethyl acetate, to give 500 mg of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06599917B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-c966ac3de3394109a200fb0fcddc1c4f |
| Source note | uspto-grants-2003_07 |