HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 2-Chloro-3-iodopyrazolo[1,5-A]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 2-Chloropyrazolo[1,5-a]pyridine | HCID 12284433 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Chloro-3-iodopyrazolo[1,5-A]pyridine | HCID 71743340 | — |
Reaction Steps
N-iodosuccinimide (1.06 g, 4.74 mmol) was added to a solution of 2-chloro-pyrazolo-[1,5-a]pyridine (27-2; 0.6 g, 3.95 mmol) in acetonitrile (18.0 mL). The resulting mixture was stirred at room temperature for 2 h and then concentrated under reduced pressure. The resulting residue was diluted with dichloromethane, washed with saturated aqueous sodium chloride solution, dried over magnesium sulphate, filtered and concentrated under reduced pressure. Purification by silica gel flash chromatography (5-10% ethyl acetate in hexanes) provided the title compound. 1H NMR (400 MHz, CDCl3) δ 8.36-8.34 (d, J=6.8 Hz, 1 H), 7.40-7.37 (d, J=8.8 Hz, 1 H), 7.26-7.23 (m, 1 H), 6.84-6.81 (m, 1 H). MS (M+1): 279.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09351973B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-026fe51dfcaf49f395c19ad0b857de4e |
| Source note | uspto-grants-2016_05 |