HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoropyridine-5-carbonyl chloride → 3-(5-(6-Fluoropyridin-3-yl)-1,2,4-oxadiazol-3-yl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoropyridine-5-carbonyl chloride | HCID 14623602 | — |
| Reactant | 3-Cyano-N-hydroxy-benzamidine | HCID 57368933 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-(5-(6-Fluoropyridin-3-yl)-1,2,4-oxadiazol-3-yl)benzonitrile | HCID 67025966 | — |
Reaction Steps
3-Cyano-N′-hydroxybenzimidamide (0.322 g, 1 mmol) was dissolved in pyridine 10 mL and 6-fluoronicotinoyl chloride (Frontier Scientific, 0.160 g, 1 mmol) was added. The reaction mixture was heated to reflux for 3 hours and then cooled to room temperature. The cooled reaction mixture was quenched with water (25 mL) and filtered. The solid was further purified with flash column chromatography (5% methanol/dichloromethane) to give the titled product. 1H NMR (300 MHz, DMSO-d6) δ 7.56-7.52 (m, 1 H), 7.85 (t, J=7.9 Hz, 1 H), 8.15-8.12 (m, 1 H), 8.43-8.41 (m, 1 H), 8.49 (m, 1 H), 8.8-8.74 (m, 1 H), 9.11-9.0 (m, 1 H) ppm; MS (DCI/NH3) m/z 267 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486979B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-543e11d18deb4aa1a479123e021b1a73 |
| Source note | uspto-grants-2013_07 |