HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-Pyridyl-pyrrolidin-1-yl-benzoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,5-Dichlorobenzooxazole | HCID 10397578 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | 3-(4-Fluorophenyl)-2-(2-pyridyl)-pyrrolidine | HCID 23356879 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Pyridyl-pyrrolidin-1-yl-benzoxazole | HCID 86750192 | — |
Reaction Steps
The crude pyrrolidine (5.9 g, 0.025M) was dissolved in 100 mL 1,4-dioxane containing N,N-diisopropylethylamine (435 mL, 0.025M). Then 2,5-dichlorobenzoxazole (4.7 g, 0.025M) was added and the resulting yellow solution was heated at reflux for 2 hours, cooled to room temperature and diluted with 250 mL ethyl acetate. The reaction mixture was washed with 200 mL portions of water and saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to obtain a yellow oil. Chromatography on silica gel with methylene chloride-methanol resulted in 4.6 g (47%) of the desired cis-+/--5-chloro-3-(4-fluorophenyl)-2-(2-pyridyl-pyrrolidin- 1-yl-benzoxazole, mp 149°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05594008 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-d66a00aa640d45e9a2356da1dd1bb551 |
| Source note | uspto-grants-1997_01 |