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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917027Generated: October 31, 2026

Hydrazine hydrate (1:1) → 4-(4-Bromo-2-chlorophenylamino)-5-chloro-6-hydrazinonicotinic acid ethyl ester

https://huagongshe.com/reaction/917027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant4-(4-Bromo-2-chlorophenylamino)-5,6-dichloronicotinic acidHCID 11661217—
Reactant4-(4-Bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid ethyl esterHCID 86596780—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
Product4-(4-Bromo-2-chlorophenylamino)-5-chloro-6-hydrazinonicotinic acid ethyl esterHCID 6886074436.1%
Product4-(4-Bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid ethyl esterHCID 86596780—

Reaction Conditions

Temperature90 °C

Reaction Steps

4-(4-Bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid ethyl ester (48) was prepared by standard methods from 4-(4-bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid. Hydrazine monohydrate (0.59 mL, 12.16 mmol) was added to a solution of 4-(4-bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid ethyl ester (48) (1.72 g, 4.05 mmol) in N,N-dimethylacetamide (20 mL). After stirring at 90° C. for 1 hour, the reaction mixture was cooled to room temperature and diluted with EtOAc. The organic layer was washed with water and brine, dried (Na2SO4) and concentrated. Purification by flash column chromatography using the Biotage system (20:1 CH2Cl2:EtOAc) provided the desired product (49) (307 mg, 18%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271178B2
Source datasetuspto-grants-2007_09
ORD IDord-4df591107a7348f7a4c0564bc75ff7eb
Source noteuspto-grants-2007_09