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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857510Generated: October 30, 2026

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

https://huagongshe.com/reaction/857510

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 numberUS07144907B2
Source datasetuspto-grants-2006_12
ORD IDord-031bbe1587c24fceaafce0f80a7cd4c8
Source noteuspto-grants-2006_12