HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → 1-(6-Azetidin-1-ylpyridin-3-yl)cyclopropanecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Azetidine hydrochloride | HCID 12308726 | — |
| Reactant | 1-(6-Chloropyridin-3-yl)cyclopropane-1-carbonitrile | HCID 22159357 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | 1-(6-Azetidin-1-ylpyridin-3-yl)cyclopropanecarbonitrile | HCID 66662706 | — |
Reaction Steps
To a solution of 1-(6-chloropyridin-3-yl)cyclopropanecarbonitrile (200.0 mg, 0.001120 mol) in 1,4-dioxane (8.00 mL, 0.102 mol) at rt were added azetidine hydrochloride (128.3 mg, 0.001344 mol), palladium acetate (25.2 mg, 0.000112 mol), and sodium tert-butoxide (288 mg, 0.00291 mol). The reaction mixture was degassed and then microwave irradiated at 150° C. for 40 min. The reaction mixture was quenched with water and extracted with ethyl acetate and dichloromethane. The crude product was purified by combiflash. LCMS: m/z 200.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07304081B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-04b12b2af6c34489bf93b754e6ae029d |
| Source note | uspto-grants-2007_12 |