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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300198Generated: November 2, 2026

N-bromobutanimide → 3-Bromo-6-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/2300198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant6-Chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridineHCID 18376034—
SolventDimethylformamideHCID 6228—
Product3-Bromo-6-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridineHCID 1837602786.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498166B1
Source datasetuspto-grants-2002_12
ORD IDord-12c0b8e66c984800801d9d9b99eeb3a6
Source noteuspto-grants-2002_12