Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | Decahydroquinoline | HCID 92911 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | HCID 178470429 | HCID 178470429 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 58501887 | HCID 58501887 | — |
Reaction Steps
To a solution of decahydroquinoline (10) (1.5 equiv) in dry dichloromethane (0.5 M) under argon was added triethylamine (1.5 equiv) followed by triphosgene (1.5 equiv). The resulting heterogeneous mixture was stirred at room temperature for 15 minutes, concentrated in vacuo. The residue was taken up in dry toluene (0.25 M with respect to amine), treated with dimethylaminopyridine (DMAP) (1.0 equiv) and triazole (9) (1.0 equiv). The resulting mixture was heated to reflux for 1.5 hours, cooled to room temperature and diluted with ethyl acetate and brine, and the aqueous and organic layers were separated. The organic layer was washed with brine, 10% aqueous HCl, then brine, and dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (ethyl acetate/hexanes) to provide ethyl 1-(decahydroquinoline-1-carbonyl)-4-(2-phenoxyphenyl)-1H-1,2,3-triazole-5-carboxylate (11) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450350B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-5ab02473171841cba6c8d6809dd5b177 |
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| Source note | uspto-grants-2013_05 |
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