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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558207Generated: October 26, 2026

Chlorosuccinimide → 4-(4-Bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid

https://huagongshe.com/reaction/558207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantSodium PyrosulfiteHCID 656671—
Reactant4-(4-Bromo-2-chlorophenylamino)-6-chloronicotinic acidHCID 21866984—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(4-Bromo-2-chlorophenylamino)-5,6-dichloronicotinic acidHCID 1166121790%

Reaction Steps

To a thick suspension of 4-(4-bromo-2-chlorophenylamino)-6-chloronicotinic acid (13.25 g, 36.8 mmol) in 350 ml DMF was added NCS (4.94 g, 37 mmol) and the suspension was stirred at room temperature for 3 days. Since the reaction did not go to completion (NMR control), an additional 1.987 g NCS was added and the mixture was stirred for 18 h, upon which the reaction went to completion. The mixture was poured into a solution of 20 g sodium metabisulfite in H2O (1 l) and the thick suspension was rest for 30 min. It was filtered, and the precipitate was washed with water, then with hexanes and it was dried in oil pump vacuo at 50° C. for 24 hours to obtain the desired compound as a white solid (13.11 g, 90%). 1H-NMR (500 MHz, DMSO-D6): δ=9.90 (s, br, 1H), 8.63 (s, 1H), 7.74 (s, 1H), 7.43-7.42 (dd, 1H), 6.99-6.97 (dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063049B2
Source datasetuspto-grants-2011_11
ORD IDord-465b1f20b5e746e790af590eb7aec95d
Source noteuspto-grants-2011_11