HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-Bromo-6-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine | HCID 18376034 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Bromo-6-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine | HCID 18376027 | 86.4% |
Reaction Steps
6-Chloro2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine (2.48 g, 10.05 mmol) was dissolved in anhydrous DMF (160 ml) and treated with NBS (1.967 g) for 1 h. The reaction mixture was partitioned between ethyl acetate and water. The organic phase was separated, washed with water, dried and concentrated to give the title compound as a brown solid (2.827 g, 86%). (CDCl3) δ 7.19 (3H, t, J 9 Hz, H-3′+H-5); 7.48 (1H, d, J 9 Hz, H4); 8.05(2H, m, H-2′); 8.49 (1H, br s, H-7); Tlc SiO2 cyclohexane:ethyl acetate (3:1) Rf 0.74 detection uv254.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06498166B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-12c0b8e66c984800801d9d9b99eeb3a6 |
| Source note | uspto-grants-2002_12 |