Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | HCID 11523287 | HCID 11523287 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | HCID 66545394 | HCID 66545394 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68469316 | HCID 68469316 | — |
Reaction Steps
A toluene solution (3.0 ml) of pyrrolidine (0.100 ml) was added to a mixture of 2-{1-[5-(2-bromophenyl)-4-methyl-4H-1,2,4-triazol-3-yl]-1-methylethyl}pyridine (360 mg), sodium tert-butoxide (136 mg), bis(dibenzylideneacetone)dipalladium (23.1 mg) and 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (31.4 mg) under a nitrogen condition, followed by stirring at 100° C. for 18 hours. The reaction solution was diluted with water (15 ml) and then extracted with ethyl acetate (15 ml). The organic layer washed with brine, dried over anhydrous magnesium sulfate and filtered and then the solvent was removed by evaporation under reduced pressure. The resulting crude product was purified by flash column chromatography (chloroform:methanol=90:10) and further purified by preparative thin layer chromatography (hexane:acetone=1:1) to obtain 81.4 mg of 2-(1-methyl-1-{4-methyl-5-[2-(1-pyrrolidinyl)phenyl]-4H-1,2,4-triazol-3-yl]ethyl}pyridine (pale yellow crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776897B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-f24347ad580e47a6b9d00f3a9ab3e115 |
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| Source note | uspto-grants-2010_08 |
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